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Category:Testing & Quality Assurance

Night Shift Mobile Services Coordinator65095756365697120

Night Shift Mobile Services Coordinator

Night Shift Mobile Services Coordinator **Department:** Operations / MOVICARE Mobile Services **Branch:** Head Office **Schedule:** Monday to Saturday, from 21:00 to 07:00 hours **Job Objective** Coordinate, supervise, and execute mobile services during the night shift, ensuring proper handling of sample collection, specimen pickups, emergencies, and patient transfers, as well as providing administrative support (data entry, billing, and quotation issuance) to guarantee comprehensive, timely, and high-quality service. **Main Responsibilities** * Coordinate and assign scheduled mobile sample collection and specimen pickup services for the shift. * Monitor scheduled services and respond to messages through official communication channels. * Address urgent and emergency requests, accompanying patients via ambulance or specimen pickup when any area is understaffed. * Enter test orders into the system, bill patients, and issue quotations, ensuring data accuracy. * Coordinate and record requested patient transfers, guaranteeing patient safety. * Provide operational support during critical situations or staff shortages in any department. * Prepare shift reports (services performed, emergencies handled, incidents, and cash movements). * Maintain effective communication with unit supervisors and administrative departments. * Comply with safety protocols, patient care standards, and internal regulations. **Requirements** * Education: Technical degree in Emergency Medical Services, Paramedicine, Nursing, or related field (preferred but not mandatory). Experience: * Coordination of services or direct patient care. * Experience in cash handling (billing) and medical test quotation is preferred. Knowledge: * Basic pre-hospital care and patient transfer assistance (preferred). * Basic laboratory/imaging and mobile services processes. * Proficiency in scheduling, data entry, and billing systems. Skills: * Organization and planning. * Ability to respond effectively in emergencies. * Clear and empathetic communication. * Direct interaction with patients and clients. **Personal Competencies** * Proactivity and accountability. * Results- and service-oriented mindset. * Teamwork and collaboration. * Problem-solving under pressure. * Commitment to patient quality and safety. **We Offer** * Competitive salary commensurate with the position. * Job stability. * Initial and ongoing training on patient care protocols, billing, and quotation procedures. * Opportunities for career growth within the organization. Employment Type: Full-time, Indefinite-term contract Salary: $10,046.52 – $12,295.68 per month Benefits: * Salary increases * Savings fund * Employee discount * Gym discount * Discounts and preferential pricing * Paternity leave exceeding statutory requirements * Company parking * Free parking * Flexible working hours * Option for indefinite-term contract * Cafeteria service * Gym service * Company phone Work Location: On-site employment

Calle Emiliano Zapata 116, Centro, 56100 Texcoco de Mora, Méx., Mexico

$MXN 10,046-12,295/year

Quality Auditor65095756217603121

Quality Auditor

**QUALITY AUDITOR POSITION (AUTOMOTIVE)** **DUE TO PRODUCTION INCREASE** **Publication Date:** January 15, 2026 **Salary:** 9,000 (MXN) \- 10,000\.00 (MXN) per month **Job Description:** We are seeking QUALITY AUDITORS due to increased production at an automotive company located in Lerma, Parque Litos (across from Plaza Sendero). Next to the security booth, please drop your job application in the mailbox and/or provide your details through this channel. INTERVIEWS ONLY. THANK YOU! Requirements: * High school diploma or technical degree * Availability to work rotating shifts * Proven experience as a quality auditor in an industrial manufacturing company, preferably automotive. Key responsibilities include: initiating first-defect stoppage upon identifying non-compliance with Quality Management System standards; identifying non-conformities versus defined standards; labeling NOK parts; completing QRAP forms; identifying customer complaints; complying with Valeo’s standard requirements. We offer: * Benefits exceeding legal requirements (transportation, cafeteria, year-end bonus, savings fund, grocery vouchers, career progression by category, educational assistance, etc.) * Available transportation routes: Colinas del Sol, Ameyalco, Zinacantepec * Communities served: Almoloya de Juárez, Santiago Miltepec, San Cristóbal H., San Andrés C., El Cerrillo, San Miguel Ameyalco, San Mateo Atenco, San Juan de las Huertas, San Antonio Acahualco, San Luis Mextepec, Seminario, Toluca, Metepec. *\- At Valeo, we comply with current labor laws and are committed to fostering a culture of belonging by hiring talent based on competencies, skills, and potential; we do not discriminate for any reason, including gender, age, ethnic origin, physical appearance, marital status, health conditions due to any illness, socioeconomic status, disability, sexual orientation, gender identity or expression; therefore, during the recruitment process, we will not request personal information.* *\- At Valeo, we commit to ensuring that our employees enjoy, day after day, a respectful workplace, free from discrimination and sexual harassment, as stipulated in our Global Code of Ethics and Business Conduct.* \-*By complying with labor legislation, our recruitment process incurs no cost to applicants and/or candidates. Thus, under no circumstances will we ask you to deliver, deposit, or transfer money or any other resource.* \-*If you require specific accommodations during the recruitment process, please inform the recruiter at the outset.* *Thank you for your attention* Job Type: Full-time Benefits: * Salary increases * Transportation assistance or service * Paternity leave exceeding statutory requirements * Company parking * Life insurance * Cafeteria service * Grocery vouchers Work Location: On-site employment Job Type: Full-time Salary: $9,000\.00 \- $10,000\.00 per month Benefits: * Transportation assistance or service * Company parking * Free parking * Life insurance * Cafeteria service * Free uniforms * Grocery vouchers Work Location: On-site employment

Av. Reolín Barejon 21, La Estacion, 52006 Lerma de Villada, Méx., Mexico

$MXN 9,000-10,000/month

Sr Investigator Management Solutions (IMS) Specialist (budget experience) hybrid CDMX Mexico (Open)65095756166915122

Sr Investigator Management Solutions (IMS) Specialist (budget experience) hybrid CDMX Mexico (Open)

**Updated:** January 7, 2026 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25104568 Not ready to apply? Join our Talent Network **Description** Sr Investigator Management Solutions (IMS) Specialist (budget experience) hybrid CDMX Mexico (Open) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** JOB SUMMARY The IMS Budget Specialist I plays an important role to the Clinical Development Services team. As the liaison between Operations Management, Site Contracts, Clinical Operations, Investigator Management Solutions Payments Team, the IMS Budget Specialist I will provide analytical insight and support reviewing site budgets, study protocols, and ensuring alignment within the dedicated clinical trial management system. JOB RESPONSIBILITIES  Analyzes and interprets the payment terms and conditions of fully executed site clinical trial agreement (CTA).  Ensures accuracy of contract budget \& clinical trial management system (CTMS) template alignment.  Inputs site budget cost utilizing the templates within CTMS.  Engages project team with the quality control of the cost structure created within CTMS.  Serves as subject matter expert for department and project teams concerning contract interpretation and development of payment strategy.  Ensures the presence of required vendor financial account details participating in clinical trial.  Ensures acquisition and completeness of tax related documentation.  Participates in payment setup issue resolution.  Liaises with internal departments including the Operations, Finance, and Legal teams.  Performs a variety of administrative functions, updates and maintains setup details and progress status of contractual site budgets in the database, and other related duties as assigned.  Works with enterprise financial systems.  Ability to multi\-task on several projects. Possess strong communication skills and be an effective team player.  Proactively participates in Investigator Payment Planning (IPP) Meetings, providing input to payment strategy planning for incoming studies.  Minimal travel may be required (up to 25%). QUALIFICATION REQUIREMENTS (please indicate if ‘preferred’)  Bachelor’s degree, or equivalent education and experience, plus minimal experience in contract administration or finance.  Requires strong communication, verbal, written, and interpersonal.  Ability to build team relationships with line management, employees, and HR team.  Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), email, and voicemail.  Ability to interact and build relationships with all levels of employees.  Ability to organize and prioritize work to meet frequent deadlines is essential.  Strong customer services skills and ability to maintain confidentiality. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

Mgr, FSP 36065095756150914123

**Updated:** January 7, 2026 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25104647 Not ready to apply? Join our Talent Network **Description** Mgr, FSP 360 Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** **Overall, the role will be responsible for three primary performance areas:** **1\) Customer Delivery and Success** * Develops and fosters strong, collaborative relationships with customers. Solicits feedback from customer PoC (s) for continuous improvement of service delivery and to strengthen customer relationships on an individual or (PoC) country\-specific level. * Responsible for delivery and compliance with agreed\-upon KPIs in relation to daily activities of their team members; develops and executes mitigation and remediation plans for non\-compliance as needed. * Responsible for headcount management, in relation to their own team, to ensure resource needs are identified and addressed in a timely fashion. Responsible for creation of job requisitions at expected level of quality. * Proactively communicates and manages customer issues through assigned escalation channels. * Ensures quality and adherence to Standard Operating Procedures/Work Instructions (SOP/WIs) and compliance with federal and local guidelines and ICH GCPs. Ensures all staff follow the required training and complete the required documentation. Provides regular compliance updates to management accordingly. * Conducts oversight visits as required for Clinical Research Associates. * Responsible for all system updates, and compliance with systems and relevant procedure and practices applicable to the customer and Syneos Health processes. **2\) Business Impact** * Responsible for knowledge sharing across their own team to disseminate best practices and lessons learned in support of the overall FSP 360 operating model. Makes informed and data\-driven decisions that positively impact their own team's performance within the business unit. * Responsible for delivering BU revenue targets by attracting and retaining the right talent. Responsible for balancing the right size and skill level team against the expected customer delivery. * May serve as a Company representative at professional meetings or seminars. 3\) **People Leadership** * Responsible for active management of team members’ performance through the established Syneos Health process; at an individual contributor level. * Verifies that team members adhere to training guidelines, maintain their training records and individual and corporate training needs are identified and addressed. * Provides administrative oversight (for example, HR processes, timecards, expense reports). * Supports team members’ professional development through coaching, providing opportunities to increase knowledge and skill levels, and by delegating tasks commensurate with skill level. * Proactively works to ensure team members’ engagement, retention and turnover rates remain within expected levels. * Demonstrates commitment to diversity, equity, and inclusion through continuous development of all staff, modeling inclusive behaviors and proactively managing bias. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Responsible for interacting and engaging with internal and external stakeholders for functional team members, acting as a Syneos Health ambassador with customers. Responsible for managing team members’ performance in line with project deliverables. Accountable for direct supervision of FSP 360 multifunctional staff. May act as an SME where country/region/functional knowledge is key.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

Safety & PV Specialist I or II (CPQA & medical devices experience) Home Based Mexico65095756134915124

Safety & PV Specialist I or II (CPQA & medical devices experience) Home Based Mexico

**Updated:** January 7, 2026 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25104865 Not ready to apply? Join our Talent Network **Description** Safety \& PV Specialist I or II (CPQA \& medical devices experience) Home Based Mexico Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** * Enter information into PVG quality and tracking systems for receipt and tracking ICSR as required. Assists in the processing of ICSRs according to Standard Operating Procedures (SOPs) and project/program\-specific safety plans as required. Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability. Enters data into safety database. Codes events, medical history, concomitant medications, and testsCompiles complete narrative summaries. Identifies information to be queried and follows up until information is obtained and queries are satisfactorily resolved. Assists in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements. * Maintains safety tracking for assigned activities. * Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, MedDRA coding as required. * Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA. * Manual recoding of un\-recoded product and substance terms arises from ICSRs. * Identification and management of duplicate ICSRs. * Activities related to SPOR / IDMP. * Quality review of ICSRs. * Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post\-marketing programs as appropriate. * Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCP, ICH guidelines, GVP, project/program plans and the drug development process. * Fosters constructive and professional working relationships with all project team members, internal and external. * Participates in audits as required/appropriate. * Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities. Qualifications: * Bachelor’s Degree in life science, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills, and abilities to perform the job. * Safety Database systems and knowledge of medical terminology required. * Good understanding of clinical trial process across Phases II\-IV and/or post\-marketing safety requirements, ICH GCP, GVP and regulations related to Safety and Pharmacovigilance. * Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), Visio, email (Outlook), Team Share (or another management/shared content/workspace) and internet. * Ability to work independently and in a team environment. * Excellent communication and interpersonal skills, both written and spoken. * Good organizational skills with proven ability to prioritize and work on multiple tasks and projects. * Detail oriented with a high degree of accuracy and ability to meet deadlines. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Roles within Pharmacovigilance \& Safety job family are responsible for providing expertise on pharmacovigilance services. This includes participating in all aspects of the medical safety team's involvement in assigned trials, such as performing medical review and clarification of trial\-related Adverse Events, providing aggregate reviews of safety information, and serving as an internal consultant to pharmacovigilance case processing teams. Provides and contributes trends and safety signal detection and risk management assessment and provides safety support to the clinical development teams. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Entry to developing individual contributor. Delivers work of limited scope, typically smaller, less complex projects. Requires theoretical knowledge of a professional area, typically obtained through education and/or prior experience.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

Safety & PV Specialist (case processing) Hybrid Mexico65095756118274125

Safety & PV Specialist (case processing) Hybrid Mexico

**Updated:** December 4, 2025 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25103060 Not ready to apply? Join our Talent Network **Description** Safety \& PV Specialist (case processing) Hybrid Mexico Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** * Enter information into PVG quality and tracking systems for receipt and tracking ICSR as required. Assists in the processing of ICSRs according to Standard Operating Procedures (SOPs) and project/program\-specific safety plans as required. Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability. Enters data into safety database. Codes events, medical history, concomitant medications, and testsCompiles complete narrative summaries. Identifies information to be queried and follows up until information is obtained and queries are satisfactorily resolved. Assists in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements. * Maintains safety tracking for assigned activities. * Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, MedDRA coding as required. * Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA. * Manual recoding of un\-recoded product and substance terms arises from ICSRs. * Identification and management of duplicate ICSRs. * Activities related to SPOR / IDMP. * Quality review of ICSRs. * Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post\-marketing programs as appropriate. * Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCP, ICH guidelines, GVP, project/program plans and the drug development process. * Fosters constructive and professional working relationships with all project team members, internal and external. * Participates in audits as required/appropriate. * Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities. Qualifications: * Bachelor’s Degree in life science, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills, and abilities to perform the job. * Safety Database systems and knowledge of medical terminology required. * Good understanding of clinical trial process across Phases II\-IV and/or post\-marketing safety requirements, ICH GCP, GVP and regulations related to Safety and Pharmacovigilance. * Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), Visio, email (Outlook), Team Share (or another management/shared content/workspace) and internet. * Ability to work independently and in a team environment. * Excellent communication and interpersonal skills, both written and spoken. * Good organizational skills with proven ability to prioritize and work on multiple tasks and projects. * Detail oriented with a high degree of accuracy and ability to meet deadlines. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Roles within Pharmacovigilance \& Safety job family are responsible for providing expertise on pharmacovigilance services. This includes participating in all aspects of the medical safety team's involvement in assigned trials, such as performing medical review and clarification of trial\-related Adverse Events, providing aggregate reviews of safety information, and serving as an internal consultant to pharmacovigilance case processing teams. Provides and contributes trends and safety signal detection and risk management assessment and provides safety support to the clinical development teams. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Entry to developing individual contributor. Delivers work of limited scope, typically smaller, less complex projects. Requires theoretical knowledge of a professional area, typically obtained through education and/or prior experience.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

Sr Clinical Data Scientist CDM (Hybrid -ARG & MEX Only)65095756101763126

Sr Clinical Data Scientist CDM (Hybrid -ARG & MEX Only)

**Updated:** December 16, 2025 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25102142\-OTHLOC\-7304\-2DH Not ready to apply? Join our Talent Network **Description** Sr Clinical Data Scientist CDM (Hybrid \-ARG \& MEX Only) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** \*\*\*This role is only open to hiring in Argentina and Mexico. Hybrid \- 2 days in office per week (Buenos Aires and Mexico City) \*\*\*Proficiency in English is required \- Please submit CVs in English. \*\*\*Previous experience within Veeva Vault is required. * Serves as Functional Lead for Clinical Data Science including primary contact for internal liaison between Clinical Data Science and Project Management, Clinical Monitoring, and other functional groups* Acts as central steward of clinical data quality, monitors risks through the holistic review of clinical and operational data, using high level knowledge of the protocol, taking into account the specific therapeutic area aspects of the protocol related to the data collected and aligning with cross functional operational plans to drive comprehensive clinical data quality* Ensures the required data elements and corresponding data quality oversight steps are identified to support the defined study analysis* Works with assigned project teams to communicate, address, troubleshoot and resolve data related questions and recommends potential solutions; escalates issues which potentially impact patient safety and study analysis* Coordinates cross functional data cleaning activities to ensure quality standards and timelines are met for clinical data deliverables Ensures the required data elements and corresponding data quality oversight steps are identified to support the defined project analysis* Drives the development of the clinical data acquisition plan and corresponding data flow diagram with the study team, assess risks associated with protocol design, study set parameters that could impact the credibility and reliability of the trial results, aligns data flow with the study protocol to ensure data collected meets regulatory and study endpoint requirements.* Drives the development of analytical tools, utilizes analytical platform/dashboard to detect potentially unreliable data that may impact the validity of the trial results Performs analytic reviews as defined in scope of work and data acquisition plan, identifies root cause to systematically resolve data issues* Monitors and communicates project progress to the Sponsor and project team including use of project status reports and tracking tools/metrics* Ensures launch, delivery and completion of all Clinical Data Sciences activities and milestones according to contractual agreement and relevant Standard Operating Procedures (SOPs), guidelines, and regulations* Review, maintain budget and identify out of scope for Clinical Sciences activities, raise to PM to be implemented in required change order* Plans, manages, and requests Clinical Data Science resources for assigned projects* Coordinates the work of the assigned Clinical Data Science team* Develops and maintains project plans, specifications, and documentation in line with SOP requirements* Maintains documentation on an ongoing basis and ensures that all TMF filing is up to date for necessary files* Participates in, and presents at internal, Sponsor, third\-party, and investigator meetings on behalf of clinical data science responsibilities* Prepares input, and participates in proposal bid defense meetings and request for proposals on behalf of clinical data science responsibilities* Plans for and creates necessary documentation to support internal and external audits; participates in such audits on behalf of clinical data sciences responsibilities* Trains and mentors new or junior team members* Maintains proficiency in Clinical Data Science systems and processes through regular training. May attend/represent the company at professional meetings/conferences* Performs other work\-related duties as assigned. Minimal travel may be required (up to 25%)**Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Responsible for the end\-to\-end coordination of cross functional data collection and cleaning activities to ensure clinical study data deliverables are fit for purpose and align with the executed contract and sponsor expectations and timelines.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

CSR Appendices Coordinator - RIMS System Exp preferred65095756085762127

CSR Appendices Coordinator - RIMS System Exp preferred

**Updated:** January 10, 2026 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25103128\-OTHLOC\-7302\-2DR Not ready to apply? Join our Talent Network **Description** CSR Appendices Coordinator \- RIMS System Exp preferred Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** **Roles and Responsibilities:** * Defines scope of Clinical Study Reports (CSR) Appendices with the document author. Coordinates and track activities and perform detailed quality reviews. Import and route documents in the regulatory information management systems (RIMS). * Confirm completeness of documents (e.g. Casebooks, Literature References) by obtaining, compiling, and organizing in the regulatory information management system (RIMS). Maintain strong knowledge of CSR and CSR Appendices and CTD structure. * Effectively communicates deliverables needed to stakeholders. Must demonstrate good interpersonal and organizational communication skills, including conflict management skills. * Effectively attends to multiple tasks within overlapping timeframes; builds positive and productive relationships that enable high quality documents to be completed on time. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Responsible for authoring of Clinical Study Report (CSR) Appendices and managing clinical and regulatory references.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

Safety & PV Specialist II - MXN Office Based - Exp in Mailbox Mgmt & All Report Processing would be preferred.65095756069505128

Safety & PV Specialist II - MXN Office Based - Exp in Mailbox Mgmt & All Report Processing would be preferred.

**Updated:** December 3, 2025 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25102866 Not ready to apply? Join our Talent Network **Description** Safety \& PV Specialist II \- MXN Office Based \- Exp in Mailbox Mgmt \& All Report Processing would be preferred. Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** Job Description* Enters information into PVG quality and tracking systems for receipt and tracking ICSR as required. * May assist in the preparation of the project plans such as Safety Management Plan. * May perform set\-up, delivery and close\-out of safety and pharmacovigilance projects. * Processes ICSRs according to Standard Operating Procedures (SOPs) and project/program\-specific safety plans. * Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability. * Enters data into safety database. * Codes events, medical history, concomitant medications, and tests. * Compiles complete narrative summaries. * Assesses information to be queried and follows up until information is obtained and queries are satisfactorily resolved. * Participates in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements. * Coordinates with data management staff concerning reconciliation of safety data between the clinical and safety databases. * Maintains safety tracking for assigned activities. * Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, and MedDRA coding as required. * Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA. * Manual recoding of un\-recoded product and substance terms arises from ICSRs. * Identification and management of duplicate ICSRs. * Activities related to SPOR / IDMP. * Quality review of ICSRs. * Quality review for the work performed by peers. * Serves as a subject matter expert in SPVG, which includes resolution of project related routine queries; mentoring, coaching, and training of new hires. * Fosters constructive and professional working relationships with all project team members, internal and external. * Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities. * Ensures distribution of all required individual expedited and periodic reports for both clinical and post\-marketing projects to the Safety Submissions team if contracted to submit the reports. * Participate in audits/inspections as required. * Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post\-marketing programs as appropriate. * Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCP, ICH guidelines, GVP, project/program plans and the drug development process. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Job Description Summary Performs safety and pharmacovigilance program delivery activities including (but not limited to) all aspects of the collection, processing, and reporting of individual cases safety reports (ICSRs), literature screening and review for safety, drug coding, maintenance of drug dictionary, Medical Dictionary for Regulatory Activities (MedDRA) coding, data management activities which includes cleaning and validation of data (xEVMPD product dictionary, manual recoding of substance/product terms arising from ISCR reports, management of duplicate ICSR cases, Quality review of ICSRs, Substances, Products, Organizations and Referential (SPOR) / Identification of Medicinal Products (IDMP) activities)) and the preparation of expedited and periodic safety reports, while adhering to all data privacy guidelines, Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), regulatory guidelines, company and project/program\-specific procedures for clinical trials and/or post\-marketing safety programs. The processing of information may include filtering, cleaning, migrating, analyzing, reporting, filing or publication of data and information.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

CRA II or Sr CRA assign to client CDMX Mexico65095756053122129

CRA II or Sr CRA assign to client CDMX Mexico

**Updated:** January 6, 2026 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25101362 Not ready to apply? Join our Talent Network **Description** CRA II or Sr CRA assign to client CDMX Mexico Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** * Conduct on\-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms * Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates * Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials * Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues * Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow\-up letters, and action plans * Collaborate with cross\-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct **Qualifications:** * Bachelor's degree in a related field or equivalent experience * Minimum of 2\-4 years of experience in clinical research monitoring * Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements * Excellent communication and interpersonal skills * Ability to work independently and manage multiple priorities * Proficiency in using clinical trial management systems and other relevant software **Certifications:** * Certified Clinical Research Associate (CCRA) or equivalent certification preferred **Necessary Skills:** * Attention to detail and strong analytical skills * Problem\-solving abilities and critical thinking * Ability to work effectively in a team environment * Strong organizational and time management skills * Proficiency in Microsoft Office Suite *We are always excited to connect with great talent. This posting is intended for an* *upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available.* We are always excited to connect with great talent. This posting is intended for a \[possible] upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Roles within Clinical Monitoring/CRA job family at the P21 level are responsible for ensuring that clinical research studies are conducted in accordance with widely accepted clinical practices. This includes conducting on\-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring. These roles involve individual contributors with responsibility in a professional or technical discipline or specialty, and may manage two or fewer employees. The majority of time is spent contributing to the design, implementation, or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Impact and Contribution Roles within Clinical Monitoring/CRA job family at the P21 level have a significant impact on the quality and integrity of clinical research studies. By ensuring adherence to clinical practices and protocols, these roles contribute to the reliability and validity of study results. They play a crucial role in the development and implementation of monitoring tools and procedures, which enhance the overall efficiency and effectiveness of clinical trials. Their contributions are essential for advancing medical knowledge and improving patient outcomes. Core Focus • Conduct thorough on\-site and remote monitoring of clinical research studies • Develop and implement tools, procedures, and processes to ensure quality monitoring • Manage defined components of projects or processes within their area of responsibility • Utilize practical knowledge of a professional area, typically obtained through education combined with experience • Maintain high standards of clinical practice and ensure the success of clinical trials

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

Medical Editor II - (Formatting Regulatory Documents) - Home Based650957560366111210

Medical Editor II - (Formatting Regulatory Documents) - Home Based

**Updated:** January 6, 2026 **Location:** Tlalnepantla, MEX, Mexico **Job ID:** 25102337\-OTHLOC\-7302\-2DR Not ready to apply? Join our Talent Network **Description** Medical Editor II \- (Formatting Regulatory Documents) \- Home Based Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** **Roles and Responsibilities:** * Defines scope of formatting of clinical and regulatory documents with the document author. Coordinates and track activities and perform detailed quality reviews. Import and route documents in the regulatory information management systems (RIMS). * Ensure document format and styles are consistent with the defined in RIMS and are consistent with the clinical and regulatory templates. Ensure document properties and naming conventions are used. Maintain strong knowledge of RIMS styes and formatting standards. * Effectively communicates deliverables needed to stakeholders. Must demonstrate good interpersonal and organizational communication skills, including conflict management skills. * Effectively attends to multiple tasks within overlapping timeframes; builds positive and productive relationships that enable high quality documents to be completed on time. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Responsible for ensuring the quality of clinical and regulatory documents are formatted to the requirements in the AbbVie style guide and document templates.

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

Support Specialist, Technical650957558949131211

Support Specialist, Technical

The Support Specialist, Technical is responsible for providing advanced technical support to Restaurant365 customers across the R365 platform. This role focuses on troubleshooting configuration, workflow, and data\-related issues in a complex SaaS / ERP environment, supporting business critical restaurant operations. The ideal candidate brings strong technical aptitude, structured problem\-solving skills, and the ability to communicate clearly with both technical and non\-technical stakeholders. ### **How you'll add value:** * Provide technical support for Restaurant365 platform * Manage customer communications through tickets, live chat, and outbound phone support * Gather detailed technical and business information from customers to troubleshoot reported issues * Diagnose configuration, workflow, and data\-related issues and deliver accurate solutions * Educate customers on Restaurant365 system functionality and best practices * Route non\-technical or non\-applicable issues to appropriate teams when necessary * Identify, document, and escalate suspected software defects with clear reproduction steps and impact details * Participate in live chat rotations * Manage a personal queue of customer tickets while meeting SLA and quality standards * Identify gaps in internal and customer\-facing documentation and contribute improvements * Assist Support leadership in rolling out new platform features or workflows * Demonstrate reliable and punctual attendance across assigned shifts, including remote or hybrid setups, while ensuring clear and timely communication with management regarding availability, scheduling changes, or unforeseen delays — particularly when supporting customers across multiple time zones ### **What you'll need to be successful in this role:** * High attention to detail, particularly when working with system configuration and financial data * Strong Excel skills, including data review and validation * Flexible and adaptable to shifting customer and team needs * Solution\-oriented mindset with the ability to troubleshoot and communicate clearly under pressure * Excellent written and verbal communication skills, with the ability to simplify complex technical concepts * Strong technical aptitude and comfort working across multiple support platforms (ticketing systems, chat, outbound phone) * Experience working with integrated systems and understanding how data flows between applications * Reliable and punctual attendance in assigned shifts and workdays including providing clear and timely communication with management regarding availability and scheduling changes **PREFERRED QUALIFICATIONS*** Bachelor’s degree with emphasis in business, finance, accounting, or information systems * Restaurant industry experience * Strong understanding of general business processes and workflows * Previous experience in a technical support or customer\-facing technical role * Experience supporting SaaS or ERP platforms (e.g., enterprise software, financial systems, or operational management tools)

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

Quality Analyst650957558448651212

Quality Analyst

Job Summary Are you passionate about ensuring safe and compliant material release while driving quality decisions and food safety risk management?* IFF is a global leader in flavors, fragrances, food ingredients and health \& biosciences. We deliver sustainable innovations that enhance products used every day. Taste: We design unique flavors with deep technical expertise that shape food and beverage brands, set trends, and elevate consumer experiences. This role is 100% onsite in Tlalnepantla, operating under rotating shifts: + 6:30 am – 2:30 pm + 1:30 pm – 9:30 pm + 8:30 am – 5:00 pm Additionally, the role works two Saturdays and rests the following two, on a rotating basis. You will join the Global Quality – Taste team, a collaborative, analytical and results‑driven group where together we create meaningful impact. Your potential is our inspiration. Where You’ll Make a Difference + Ensure the safe and compliant release of raw materials and materials. + Perform physical‑chemical and sensory analyses of raw materials and finished products (liquids, powders, spray, emulsions). + Conduct root‑cause investigations for out‑of‑specification (OOS) results and quality deviations. + Make quality and food safety decisions regarding materials with deviations. + Draft and update standard operating procedures (SOPs). + Promote and comply with safety, environmental, quality and food safety practices. + Report unsafe conditions and propose improvements in SHE. + Perform sampling of raw materials and follow up on supplier deviations. + Review performance indicators (KPIs), trends and improvement opportunities. What Makes You the Right Fit + Degree in Food Engineering, Chemistry, Biotechnology or related fields. + 2–3 years of experience in quality control in food, ingredients or regulated industries. + Proficiency in SAP Quality (QM) and handling notifications. + Knowledge of analytical instruments, chromatography, sampling and quality control principles. + Strong decision‑making ability in assessing material quality. + Critical thinking, problem‑solving and analytical mindset. + Effective communication to collaborate with Production, Maintenance and SHE. + Availability to work rotating shifts and a two‑Saturdays‑on / two‑Saturdays‑off schedule. + Strong compliance orientation, documentation discipline and attention to detail. How You Will Make an Impact + Making informed decisions that protect product quality and food safety. + Supporting continuous improvement through data analysis and deviation follow‑up. + Operating with strong alignment to safety, quality and regulatory standards. Why Choose Us? + Direct impact on the quality of the Taste business product portfolio. + Technical and professional development within a global environment. + Structured and predictable rotating shift system. + Culture focused on operational excellence, safety and food safety. + Exposure to advanced quality systems, standards and technologies. + Collaboration with multidisciplinary teams across plant operations. We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity \& expression, sexual orientation, or disability. Visit IFF.com/careers/workplace\-diversity\-and\-inclusion to learn more

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

CCTV INSTALLATION TECHNICIAN650956419873291213

CCTV INSTALLATION TECHNICIAN

Join us as a **CCTV Installation Technician**! We are a company committed to excellence in service and the well-being of our workforce. **Requirements** * Minimum education level: high school or equivalent (technical training preferred). * Experience installing CCTV, access control systems, and electronic security systems. * Knowledge of CAT cable termination. * Proficiency with tools (drill, cable punch-down tool, tester, etc.). * Cable laying and routing (UTP, coaxial, and power cables). * Assistance with work at heights. * Preferred: basic knowledge of electricity, electronics, or networking. * Experience installing and maintaining CCTV equipment. * Willingness to learn and follow established procedures. * Responsible, punctual, and service-oriented. * Ability to work effectively in a team. * Desire for professional development and growth. **Main Responsibilities** * Installation and basic support of security cameras (CCTV). * Support in data network and structured cabling installations. * Basic installation of IP telephony, access control, and alarm systems. * Conduit installation, cable laying, and termination (UTP, raceways, and conduits). * Support in preventive and corrective maintenance. * On-site work at client locations. * Basic completion of service reports and assistance to the lead technician. **We Offer** * Salary: **$11,000 net monthly** * Statutory benefits * Growth opportunities * Schedule: * Monday to Friday, **09:00 to 18:00 hrs** * Saturdays, **09:00 to 13:00 hrs** **Interested candidates:** Submit your CV via this platform or WhatsApp **55 4875 5124**. Job type: Full-time Salary: Up to $11,000.00 per month Benefits: * Employee discount * Option for an indefinite-term contract Work location: On-site employment

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

$MXN 11,000/month

Senior Research Analyst - Oil Supply650956412788491214

Senior Research Analyst - Oil Supply

Wood Mackenzie is the global data and analytics business for the renewables, energy, and natural resources industries. Enhanced by technology. Enriched by human intelligence. In an ever\-changing world, companies and governments need reliable and actionable insight to lead the transition to a sustainable future. That’s why we cover the entire supply chain with unparalleled breadth and depth, backed by over 50 years’ experience. Our team of over 2,400 experts, operating across 30 global locations, are enabling customers’ decisions through real\-time analytics, consultancy, events and thought leadership. Together, we deliver the insight they need to separate risk from opportunity and make confident decisions when it matters most. **WoodMac.com** **Wood Mackenzie Brand Video** **Wood Mackenzie Values** * Inclusive – we succeed together * Trusting – we choose to trust each other * Customer committed – we put customers at the heart of our decisions * Future Focused – we accelerate change * Curious – we turn knowledge into action **Wood Mackenzie's Research** Wood Mackenzie’s research groups provide integrated subscription, research and advisory services to inform and support our client’s commercial and strategic decisions in the complex and rapidly changing energy industry across all sectors of the economy. Combining our deep knowledge of transport, battery technologies and raw material supply chains with our expertise in power, renewables, storage, and fuels modelling, and emerging technologies like hydrogen and CCUS, Wood Mackenzie can provide data and insight spanning the entire energy value chain. We cover supply chains, technology costs, policy and market issues, fundamentals\-based outlooks, scenario modelling, price forecasting, asset valuation, and commodity market landscapes. **Team Profile** Wood Mackenzie’s Oil Supply team provide granular analysis and commercial insight into global liquids supply in both the short and long\-term. The team sits within the Oil and Chemicals commodities group, but collaborates extensively across different teams, including upstream, downstream, chemicals and oil markets. Our oil supply analysis forms a key part of our integrated market outlooks, supporting our crude oil price outlooks. **Role Purpose** This role is for a **Senior Analyst** in the team, with the focus to analyse short\- and long\-term supply trends, both regionally and globally. We are seeking an enthusiastic candidate who is passionate about the future of the oil industry and how it will develop in the coming decades to meet the needs of society in a sustainable manner. Candidates will require an analytical mindset, an eye for detail, strong communication skills and have a flair for presenting to audiences \- both in small and large groups. The successful candidate will join a global team of world\-class industry experts undertaking industry\-leading fundamental research and modelling of all aspects of the oil and chemicals value chains. Our research and consulting services provide clients with unique insight into the future of the oil and refining sector and the markets which it serves, giving them a robust platform to make the best commercial and strategic decisions. The role offers the opportunity to develop modelling and forecasting techniques and industry knowledge through regular interaction with other members of the global Oils and Chemicals team. **Main Responsibilities** * Lead our short and long\-term supply analysis for specific regions, maintaining relevant data through secondary and primary research and that data quality, consistency and accuracy reflect market realities. * Work closely with colleagues in other Wood Mackenzie research teams to build a robust, integrated view of how supply will adapt through the energy transition. * Pro\-actively contribute to methodology and modelling improvements. * Present the outlook for regional supply to clients and prospects in meetings and via web\-calls where appropriate. * Work with the product managers of the evolving suite of oil market product offerings to deliver high quality content, which clearly communicates our analysis to clients. Contribute to development plans for the products, providing ideas and support for enhancements and improvements. * Respond to internal and external enquiries regarding oil supply in a timely and professional manner. * Work closely with the sales and marketing teams to service clients and grow the client base. **Knowledge and Experience** * You have demonstrable interest and relevant experience in the upstream oil sector. Experience as an engineer or analyst in oil market analysis would be a distinct advantage. * You have a knowledge of oil supply fundamentals with ability to develop and maintain short and long\-term models. * You have effective interpersonal and communication skills, including the presentation skills necessary to articulate your findings to industry participants at a range of levels. This is coupled with your ability to communicate highly complex and detailed market analysis, delivering messages that are easily understood. * You can learn established processes and procedures carefully, with attention to detail, while also an ability to improve and evolve current processes. * Strong analytical and problem\-solving capabilities. Interested in using both qualitative and quantitative methods to answer market questions. * Self\-driven. Capable of switching between the roles of an individual contributor and a collaborative leader. * Strong communication skills. Comfortable interacting with senior levels amongst customers and industry stakeholders. * Passionate, with a deep intellectual curiosity, about the energy and commodity industries. * Growth mindset, with a desire to develop yourself and others in the team. * Passion for using Artificial Intelligence and all the new analytical methods available to help us grow faster and better. * Strong excel skills required. Understanding of Python an advantage. **Equal Opportunities** We are an equal opportunities employer. This means we are committed to recruiting the best people regardless of their race, colour, religion, age, sex, national origin, disability or protected veteran status. You can find out more about your rights under the law at www.eeoc.gov If you are applying for a role and have a physical or mental disability, we will support you with your application or through the hiring process.

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

Electronic Equipment Repair Technician650956366104351215

Electronic Equipment Repair Technician

**DIEBOLD NIXDORF DE MEXICO S.A. DE C.V. is seeking an Electronic Equipment Repair Technician at Lago Esmeralda - Atizapán de Zaragoza, State of Mexico** ------------------------------------------------------------------------------------------------------------------------------------------------------ **Summary of Responsibilities:** Repairs and tests mechanical and electromechanical assemblies and subassemblies. Works from drawings, sketches, wiring diagrams, and written or verbal instructions to understand and perform repair and/or testing activities. Ensures work complies with established technical, product, and quality requirements. Key Responsibilities: * Become familiar with Electronic Repair Technician practices and procedures. * Under guidance, performs routine Electronic Repair Technician tasks, including: identifying, isolating, and correcting product failures. * Disassembles, cleans, and refurbishes assigned product components. * Assists in performing tests, recording results, and reporting findings. Develops practical knowledge of DN product lines and associated diagnostic and test procedures. * Participates in regular product/repair/maintenance training (on-the-job, classroom, and online). * Learns and adheres to DN policies, electrostatic discharge (ESD) sensitivity requirements, and safety standards. * Learns and gains understanding of operational manuals, equipment capabilities, and manufacturer instructions. * Understands drawings, electrical schematics, and diagrams, as well as their use for diagnosing and resolving anomalies. * Assists in special projects as assigned. **Requirements:** * Education: Minimum of high school diploma or completed technical degree. * Experience: Minimum 0–2 years of experience in electronic equipment repair areas. (Professional internships or academic projects may be considered.) * Strong verbal and written communication skills. * Work location: Atizapán de Zaragoza, Esmeralda Zone. **Desired Education Level:** Upper Secondary **Desired Experience Level:** Entry Level **Departmental Function:** Maintenance and Repairs **Industry:** Manufacturing, Consumer Goods **Skills:** * Attention to Detail * Organization * Teamwork *This job posting originates from the Talenteca.com job board:* *https://www.talenteca.com/anuncio?j\_id\=696941cd6100002600947b28\&source\=indeed*

C. Pioneros del Cooperativismo 214, Mexico Nuevo, 52966 Cdad. López Mateos, Méx., Mexico

Traffic and Logistics Coordinator650956365628191216

Traffic and Logistics Coordinator

Job Objective Coordinate and monitor traffic operations during the night shift, ensuring timely dispatch of units, operator supervision, and compliance with established routes, schedules, and procedures. Main Responsibilities * Coordinate unit departures and arrivals during the night shift. * Assign trips and monitor operators en route. * Monitor units and report incidents. * Maintain constant communication with operators and internal departments. * Record trips, schedules, and operational events. Requirements * Education: Completed high school or technical degree (bachelor’s degree preferred). * Experience: 1 to 3 years in traffic or logistics (preferred). * Basic knowledge of routes, dispatching, and operator control. * Computer and traffic system proficiency. Competencies * Organization and control * Effective communication * Decision-making * Working under pressure * Availability for night shift Job Type: Probationary period Contract Duration: 3 months Salary: $14,000.00 - $16,000.00 per month Work Location: On-site employment

10 de Junio 3, Villas de Santa María, Centro, 55785 Santa María Tonanitla, Méx., Mexico

$MXN 14,000/year

Backend Java Developer650956365000991217

Backend Java Developer

API's Developer **Job Description:** We are looking for an API Developer passionate about quality, speed of delivery, and teamwork. The ideal candidate must have experience developing high-performance API solutions, ensuring scalability, security, and process optimization, while also fostering continuous improvement and innovation within an agile environment. **Responsibilities:** * **Quality Development**: Build robust, scalable, and secure solutions with a strong focus on code quality. * **Speed of Delivery**: Meet established deadlines without compromising development quality. * **Team Collaboration**: Collaborate closely with other developers, designers, and project management teams. * **Optimization and Performance**: Improve API efficiency and performance through optimization practices. * **Innovation and Continuous Improvement**: Propose and implement improvements to processes and technologies used. * **Incident Management and Support**: Resolve technical incidents and provide timely support to ensure API operational continuity. **Functions:** * **Needs Identification**: Analyze user requirements and translate them into technical specifications. * **RESTful API Development**: Design and maintain efficient, scalable RESTful APIs. * **Data Integrity**: Ensure data quality and consistency across APIs. * **Technical Documentation Development**: Document processes, methodologies, and technical specifications. * **Security and Authentication Management**: Implement security mechanisms to protect APIs and data. * **API Maintenance and Support**: Provide ongoing support and perform enhancements on existing APIs. * **Production Deployment Monitoring**: Monitor and track production deployments. * **Quality Testing**: Conduct quality testing using various tools and methodologies. * **Technical Incident Management**: Address and manage technical incidents to ensure proper API functionality. **Technical Requirements:** **Intermediate Level:** * **Java 17+** / **Spring Boot** * **Swagger** * **Artifactory** * **Gradle / Maven** * **Git and GitLab** * **JUnit and Mockito** * **Postman** * **Artillery and JMeter** * **SonarQube** **Basic Level:** * **Docker** * **Oracle, PL/SQL, SQL (DDL, DML)** * **MongoDB** * **AWS (Elastic Container Service - ECS, CloudWatch, S3)** * **Jira** **Desired Skills:** * **Scalability and Maintainability**: Ensure APIs are scalable and easy to maintain over time. * **API Security Management**: Implement security best practices to protect data. * **Stakeholder and Client Collaboration**: Work effectively with clients and other stakeholders to identify needs and deliver appropriate solutions. * **Version and Deployment Management**: Manage versions and ensure correct API deployment. * **Testing and Code Quality**: Apply agile methodologies and automated testing to ensure delivered code quality. **We Offer:** * **Competitive salary** and additional benefits. * Opportunity to **work with cutting-edge technologies** in a dynamic team. * **Professional growth opportunities** and continuous training. * **Statutory benefits** * **SGMM** * **Work Mode: On-site** If you're passionate about technology and excited about API development, we want to meet you! **Send a WhatsApp message to 5516404825 with the job title “API's Developer”** Employment Type: Full-time Salary: $30,000.00 - $35,000.00 per month Benefits: * Major medical expense insurance Work Location: On-site employment

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

$MXN 30,000-35,000/year

M26116 Payroll Analyst650898485299221218

M26116 Payroll Analyst

CIMMYT is a cutting\-edge, non\-profit, international organization dedicated to solving tomorrow’s problems today. It is entrusted with fostering improved quantity, quality, and dependability of production systems and basic cereals such as maize, wheat, triticale, sorghum, millets, and associated crops through applied agricultural science, particularly in the Global South, through building strong partnerships. This combination enhances the livelihood trajectories and resilience of millions of resource\-poor farmers, while working towards a more productive, inclusive, and resilient agrifood system within planetary boundaries. CIMMYT is a core CGIAR Research Center, a global research partnership for a food\-secure future, dedicated to reducing poverty, enhancing food and nutrition security, and improving natural resources. For more information, visit cimmyt.org CIMMYT is seeking a dynamic, self\-motivated, and service\-oriented professional for the position of Payroll Analyst with strong focus on laws and regulations related to social security, including social security contribution requirements, retirement plan contributions, payroll taxes and other related legal aspects to work in the Human Resources Unit. The position will be based at CIMMYT headquarters in Texcoco, near Mexico City. **Specific duties:** * Payroll system and IMSS employee movements (high, re\-entry and retirement) * Calculation of priority settlements * Determination and submission of the bimonthly variable of the different employer records on the dates established in the social security law. * Generate the calculation and reconciliation of the monthly and bimonthly payment of the IMSS and INFONAVIT vs emissions vs SUA vs. Payroll on the dates established in the fiscal legislation. * Confirmation of INFONAVIT credit through the platform and validation in each payroll period. * Attention and follow up to IMSS\-INFONAVIT requirements and procedures. * Reconciliation of accounts related to payroll process, reimbursement of disabilities and CIGNA insurance. * Follow up of information for Actuarial Calculation and audits. * Administration of the food coupons. * Fillinf the report of HQ disabilities and the stations to maintain internal control within the payroll area in relation to the sequence and payment thereof. * Concentration and follow\-up of the labor risk formats (ST7\-ST2\- STPS) to present the annual declaration on the dates established in the Social Security Law **Requirements** * The candidate must have a bachelor’s degree in accounting or a related area. * The candidate must have 4 to 5 years of working experience in Payroll and Social security * The candidate must have an intermediate level of English, (English test will be administered; candidate must score a minimum of B1 as per CEFR). * The candidate must have an advance knowledge of ERP’s and Microsoft Office * The candidate must have demonstrated experience in the preparation of relevant and timely financial management information including the use of visual information. * The selected candidate must exhibit the following competencies: Critical thinking, Teamwork, Client * Orientation, Problem\-Solving decision\-making, Negotiation, and Conflict resolution. **Benefits** CIMMYT offers an attractive remuneration package and support for continuous professional development. In addition to the provisions of the Mexican Labor Law our package of benefits includes year\-end bonus (40 days), vacation premium (56%), life and medical insurance, supermarket coupons, savings fund, social Mexican benefits (IMSS, SAR / Infonavit).

Av. Juárez Nte. 227, Centro, 56100 Texcoco de Mora, Méx., Mexico

Data Steward, Scent650898484811541219

Data Steward, Scent

Job Summary What’s your next big career move? If it involves driving meaningful change, we should talk. IFF is a global leader in flavors, fragrances, food ingredients and health \& biosciences. We deliver sustainable innovations that elevate everyday products. Scent: Harnessing the full emotional power of scent, driven by pioneering creativity, science, consumer expertise and a mindful approach to fragrance design Location \& Work Style The role is based in Tlalnepantla (Hybrid role). Be part of a dynamic, innovative, and collaborative team where together we can achieve greatness and make a real impact. ✨ *Your potential is our inspiration.* Where You’ll Make a Difference * Act as the subject matter expert for fragrance formulas, ingredients, and regulatory records. * ️ Define and enforce data standards, policies, and taxonomies for scent\-specific data. * ️ Manage metadata, lineage, and technical specifications for fragrance data. * ✅ Apply governance policies to ensure consistency across R\&D, production, and marketing. * Monitor and resolve data quality issues, ensuring accuracy and compliance. * Track and report key data quality metrics and health indicators. * Ensure regulatory compliance and secure access to proprietary formulas. * Collaborate with cross\-functional teams to resolve data issues and enable analytics. * Drive continuous improvement in data management processes and tools. ✅ What Makes You The Right Fit * Bachelor’s degree in Data Management, Information Systems, Chemistry, or related field (Master’s is a plus). * 3–5\+ years of experience in data governance, stewardship, or quality roles. * Experience with large, complex chemical or material datasets. * Skilled in SQL for querying and profiling data; Python or R is a plus. * ️ Familiarity with governance tools (Atlan, Collibra, Informatica, Talend). + ️ Knowledge of modern data platforms (Snowflake, Redshift, Databricks). * Understanding of metadata, lineage, and master data management. * Knowledge of GDPR, CCPA, and compliance frameworks. * Strong communication and collaboration skills across technical and business teams. ✨ How Would You Stand Out? * Experience in fragrance industry, R\&D, or analytical labs. * Familiarity with chemometric analysis and laboratory instrumentation. * Ability to design and deliver data literacy programs for scientific teams. Why Choose Us? * Join a global leader in fragrance innovation and data excellence. * Opportunities for professional growth and cross\-functional collaboration. * ️ Work with cutting\-edge data platforms and governance tools. * Competitive compensation and benefits package. * Inclusive and diverse work environment that values your expertise. * ✨ Make a real impact on the future of fragrance creation. We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity \& expression, sexual orientation, or disability. Visit IFF.com/careers/workplace\-diversity\-and\-inclusion to learn more

Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico

Partner Enablement Instructional Designer650898484478731220

Partner Enablement Instructional Designer

**Join Udemy. Help** **define****the future of learning.** Udemy is an AI\-powered skills acceleration platform built to help people and teams grow. It’s personalized, practical, and focused on real\-world impact. Our mission is simple: to transform lives through learning. Your work helps people around the world build skills they can use, whether they’re picking up something new or leveling up to stay ahead. Over 80 million learners and 17,000 businesses already learn with Udemy. If you’re excited by change, energized by learning, and ready to have a real impact, you’ll feel right at home. **Where we Work** Udemy is a global company headquartered in San Francisco, with additional U.S. offices in Denver and Austin, and international hubs in Australia, India, Ireland, Mexico, and Türkiye. ***T******his is an in\-office position, requiring three days a week in the office (Tuesday, Wednesday, Thursday) and flexibility on Mondays and Fridays*****.** **About your skills** * Design and Development Expertise *: Design and develop a world class learning experience, including microlearnings, in the flow of work for our partner ecosystem* * Project Management*: be able to manage an end\-to\-end project and ensure the project is delivered on time, within the budget and ensure the right people provide input* * *AI Concepts :**understand AI concepts like Machine Learning, Generative AI and Prompt Engineering, data analysis for insights, and using AI tools to automate tasks (like transcription, translation, video editing) and create adaptive, accessible, and engaging learning experiences, focusing on human oversight for quality and ethics* * Cross\-Functional Collaboration*:* *have strong strategic communications and cross functional skills. You can bring people together, getting behind ideas and recommendations working towards a shared goal, breaking down silos to leverage diverse skills for better problem solving, innovation, and achieving complex projects that span functions, leading to stronger outcomes. People like working with you.* **About this role** This role is focused on planning, designing and creating learning offerings for partners for our top strategic priorities. This includes enablement programs for business GTM initiatives, specific Partners and Partner skills development. The Learning Instructional Design Associate will co\-ordinate and execute the instructional design for partner skills courses as well as broader selling skills learning journeys, ensuring that the learning provided meets the business objectives, is exciting and well\-structured for the audience and actionable for immediate application. The role is strategic due to the variety of topics, broad range of stakeholders and complexity due to the number of offerings. **What you’ll be doing** Design and Development Expertise * Create best in class AI learning curricula: support the design and development of enablement initiatives for Sales \& CS processes, Udemy systems and products, industry knowledge, and the Udemy corporate vision. * Consult on projects and recommend design ideas: partner with sales \& CS enablement teams, subject matter experts, and facilitators to establish content needs * Partner with enablement teams to ensure a learning needs analysis has been conducted to identify the knowledge, skills, and competencies required of learners for them to complete job tasks efficiently and effectively * Transform technical content into engaging and immersive learning experiences * Create courses and learning content using an array of eLearning and video development tools (Articulate Storyline, Articulate Rise, Camtasia, Vyond, Adobe Photoshop and InDesign) and always consider Udemy products first * Create virtual live courses and workshops based on design concepts for maximum interactivity and learner engagement, using virtual deployment platforms, eg Zoom * Write and edit storyboards, interactive scripts, and other learning documentation * Design and develop additional learning materials including PowerPoint presentations, virtual and live instructor\-led training sessions, participant/facilitator guides, and job aids * Ensure content is clear, accurate, consistent, and grammatically fluent * Design visually appealing, professional content that adheres to Udemy brand guidelines Industry Expertise * Audit courses and assist with evaluating the effectiveness of learning programs, making recommendations accordingly * Apply an understanding of adult learning theories and methodologies * Remain current with industry trends and practices; challenge yourself to continually innovate and improve your work and the work of the team as a whole * Work with learning business partner to plan for launch and reporting courses you create Project Management Expertise * Successfully manage multiple projects to achieve project goals/meet deadlines * Work collaboratively with diverse stakeholders to achieve project goals * Build relationships with cross\-functional partners to understand how global audience of learners engages with your content * Work collaboratively with learning vendors where applicable to create and deliver high quality, best in class Udemy relevant enablement **What you’ll have** * **2\+ years of corporate instructional design experience** * **Portfolio of work samples demonstrating knowledge of instructional design models and adult learning theories, as well as proficiency in eLearning authoring tools and other design tools** * **Excellent oral and written communication and presentation skills** * **Bachelor’s or Master’s degree in instructional design, education, communications, or related field with writing emphasis** * **Highly organized and quality\-oriented with attention to details while keeping a good overview** * **Strong team player who can work collaboratively with colleagues on all levels of the organization especially in virtual and international teams** * **Experience with the following tools preferred: HighSpot, Gong, Articulate Storyline, Articulate Rise, Camtasia, Vyond, Zoom, ChatGPT, NotebookLM. Optional: Adobe Photoshop and InDesign, AirTable, project management.** * **Input to Asana to ensure the Field Dashboard is up to date for tracking \& impact measurement** * **Ability to leverage analytics and performance data to assess the effectiveness of learning programs and drive continuous improvement** * **Proven track record of managing multiple projects simultaneously with effective prioritization and stakeholder communication** * **Ability to bring creative and fresh approaches to learning design to drive learner engagement and knowledge retention.** **Posting Date:** December 31st, 2025 **Application Window:** We anticipate the application window will be open until January 19th, 2026\. Based on business needs, this opportunity may remain posted beyond or closed before the anticipated application window. ###### **\#LI\-KC2** At Udemy, we strive to be transparent around compensation. Actual compensation for this role is based on several factors, including but not limited to job\-related skills, qualifications, experience, and specific work location due to differences in the cost of labor. In addition to a base salary, this role is also eligible for equity. Hiring Compensation Range $456,000—$570,000 MXN**Why work here?** **You’ll grow here.** Learning is part of the job. You’ll get full access to Udemy courses, a monthly UDay to invest in yourself, and a budget to spend on whatever helps you improve. Many people are diving into AI lately, but what you focus on is up to you. **AI is real here.** We use it in the way we learn and the way we work. You’ll have the space and tools to experiment, apply, and get better at using AI in practical ways. **You’ll own your work.** We trust people to lead, make decisions, and follow through. You don’t need to wait for permission or layers of approval to have an impact. **You’ll build with others.** We collaborate openly and shape ideas together. Everyone has a voice, and good thinking is welcomed from any direction. **You’ll see your impact.** What you build helps people grow their skills, change their careers, or find a path forward. You’ve got the experience, why not use it to help others gain theirs? *Bring your curiosity. We’ll bring the platform and the support. Let’s* ***LEARN*** *together.* **Our Benefits Start with U** Our benefits start with you and were built to provide you and your family with the protection and care you need, making it easy to access the right coverage when you need it most. Benefits vary by region, and we encourage applicants to review our Australia Benefits, India Benefits, Ireland Benefits, Mexico Benefits, Turkiye Benefits \& US Benefits, pages to get an understanding of some of the benefits we offer. For details on region\-specific benefits, please refer to the information provided during the hiring process. *Benefits outlined are provided as a general overview and may vary depending on the location, role, and employment classification. All benefits are subject to change at the discretion of the organization and in accordance with applicable laws and policies.* *At Udemy, we value diversity and inclusion and consider qualified applicants without regard to race, color, religion, sex, national origin, ancestry, age, genetic information, sexual orientation, gender identity, marital or family status, veteran status, medical condition, or disability. We understand that not everyone will match each of the qualifications. However, we also realize that everyone has unique experiences that can add value to our company. Even if you think your background might not perfectly align, we'd love to hear from you!* ***Information regarding data privacy is available within the*** ***Udemy Careers Privacy Notice******.***

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

$MXN 456,000-570,000/year

IT Helpdesk Specialist650897316449301221

IT Helpdesk Specialist

**OUR COMPANY:** EOS IT Solutions is a Global Technology and Logistics company, providing Collaboration and Business IT Support services to some of the world's largest industry leaders, delivering forward\-thinking solutions based on multi\-domain architecture. Customer satisfaction and commitment to superior quality of service are our top business priorities, along with investing in and supporting our partners and employees. We are a true International IT provider and are proud to deliver our services through global simplicity with trusted transparency. **WHAT YOU WILL DO:** As a Helpdesk Specialist, you will play a crucial role in ensuring the smooth and efficient operation of our organization's information technology infrastructure. You will be responsible for providing technical support to our internal and external stakeholders, resolving issues promptly, and maintaining a high level of customer satisfaction. Your expertise and dedication will contribute to the overall success of our IT department and the company as a whole. This role is 100% onsite in Mexico City, MX **KEY RESPONSIBILITIES:** * Processing of laptop replacement queue. * First point of contact within Global Service Desk (GSD) support channels including (but not limited to) ITSM ticketing platforms, Slack support channels (as determined by GSD leadership), and in\-office walk\-up support. * Respond to common technical difficulties, training and guidance requests from user base involving desktop/laptop hardware and software/applications * Monitoring and actioning appropriate ITHELP Jira queues as directed by GSD * Software Provisioning / Deprovisioning within scope/access constraints of role within GSD * Adherence to standard escalation processes for IT tickets * Adherence to standard ticket handling practices as directed by GSD (e.g., components, labels, other ITSM related fields) * Slack Administration (within role access constraints) * Google Workspace Administration (within role access constraints) * Laptop imaging and set up for new and existing employees. * Ensure Standard Operation Principles (SOPs) are followed, and all processes and procedures adhere to EOS company policy/standards. * Primary ownership of cadenced (as directed by GSD) office desk workspaces for peripheral testing, replacement and general tech readiness * Other IT/Helpdesk support as needed. **REQUIRED CRITERIA:** * Technical certification or bachelor's degree in IT\-related field preferred. * Ability to communicate and write proficiently in a corporate environment. * 3\-6\+ years of proven experience in a helpdesk or technical support role. * Strong understanding of Apple operating systems, software applications, and network systems. * Excellent problem\-solving and communication skills. * A commitment to providing exceptional customer service. * Ability to work independently and in a team\-oriented environment. * Familiarity with IT service management (ITSM) and helpdesk software is a plus. *The EOS pay range for this job is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, experience, education, knowledge, skills, and abilities, as well as internal equity, market data, or other laws.* *EOS is committed to creating a diverse and inclusive work environment and is proud to be an equal opportunity employer. We invite you to consider opportunities at EOS regardless of your gender; gender identity; gender reassignment; age; religious or similar philosophical belief; race; national origin; political opinion; sexual orientation; disability; marital or civil partnership status or other non\-merit factor.* *\#LI\-AM1* *\#Onsite* *\#NAMERHV*

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

Automation Tester650897291578891222

Automation Tester

Location Mexico City, Mexico This job is associated with 2 categories See all At NTT DATA, we are more than a technology company: we are a global team of over +190,000 professionals present in +50 countries. We collaborate across key sectors such as telecommunications, financial services, industry, energy, public sector, and healthcare, delivering innovative solutions that drive digital transformation. Our mission is to provide technological, strategic, and business solutions—spanning from consulting to application development and maintenance. We achieve this through teamwork, the talent of our people, and a culture that challenges the status quo, always betting on innovation that brings us closer to the future. What are we looking for? Automation Tester with at least 1 year of experience in test automation and preferably with knowledge in the Telecommunications (Telco) sector. Location: CDMX (near Diana Cazadora) Work modality: On-site Bachelor’s or Engineering degree in Systems or related field; current student or graduate We offer: * Competitive salary commensurate with experience under a 100% payroll scheme * Statutory benefits * Work-life balance policy (Concilia) NTT offers one of the most comprehensive training programs, focused on 6 core areas covering competencies: \-NTT Assets \-Soft Skills \-Management \-Technical \-UN \-Languages What profile do we seek at NTT? We seek capable individuals with ambition and drive, eager to learn and who embrace the company’s purpose as their own. What technical knowledge should you have? * Design, develop, and maintain automated test scripts for web, mobile, microservices, and API applications. * Collaborate with manual testing teams to analyze requirements and prioritize automation of the test case backlog. * Execute and monitor automated tests, ensuring software quality. * Identify, report, and track defects detected during execution. * Document developed scripts and generate test result reports. * NICE TO HAVE: Ensure automated tests are properly integrated into CI/CD pipelines. * Continuously optimize and improve existing automation scripts. * Attend site as required for specific tests or technical validations. What will be your responsibilities? * Responsible for automating tests for web, mobile, microservices, and API applications, collaborating with manual testing teams to convert the script backlog into automated tests. On-site attendance availability according to project needs is mandatory. * Knowledge of automation tools such as Selenium, Appium, RestAssured, Postman, or similar. * Experience in testing web, mobile, microservices, and API applications. * Programming skills (Java, Python, JavaScript, or another relevant language). * NICE TO HAVE: Knowledge of integrating automated tests into CI/CD pipelines (Jenkins, GitLab CI, etc.). * Availability to attend site as required by project needs. * Ability to work collaboratively within a team and with manual testers. * Experience using test management tools such as JIRA, TestRail, or similar. Want to know more? If you’re interested in learning more about our opportunity, contact us at mexico.reclutamiento@nttdata.com or +52 55 8503 9100. You can find more information about NTT DATA at www.nttdata.com. At NTT DATA, all our selection processes are based on talent and equal opportunity. We do not discriminate on the basis of age, gender, sexual orientation, marital status, religion, race, nationality, or disability.

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

Tester - Testing650897291421461223

Tester - Testing

Location Mexico City, Mexico This job is associated with 2 categories See all NTT Data Company, we are all the people who make it up. A team of more than 139,000 professionals, as diverse as the 50 countries where we operate and the different sectors in which we develop our activities; telecommunications, financial institutions, industry, utilities, energy, public administration and healthcare. What is our mission? To offer technological, business, strategy, application development and maintenance solutions, being a benchmark in consulting. All thanks to collaboration among teams, the human quality of our people and our refusal to settle for the status quo—we constantly seek innovation that brings us closer to the future. We are currently looking for a: Tester - Testing who will carry out the following activities: Minimum 4 years of experience in: * Knowledge of Software Testing Methodologies. * Experience in designing and executing functional tests, regression tests, and integration tests. * Familiarity with methodologies such as ISTQB, Scrum, and DevOps for managing testing cycles. * Experience leading Testing Teams, generating testing strategies and work plans. * Experience in the Insurance Sector and related Regulations. * Knowledge of business processes and common systems in the insurance sector (e.g.: policies, claims, quotations). Main responsibilities: Testing Strategy Planning and Management. Define and oversee the testing strategy (manual and automated) to ensure software quality. Prioritize and assign testing tasks to the team based on criticality and business impact. Test Design and Execution. Create detailed test cases based on project requirements and ensure their efficient execution. Ensure traceability of test cases with functional and non-functional requirements. Collaboration and Communication with Project Teams. Act as a liaison between development, quality assurance, and business teams, ensuring quality objectives are met. Generate detailed reports on test status, coverage, and defects found, proposing solutions for continuous improvement. Is English required? Intermediate level Benefits: * Salary commensurate with experience under a 100% payroll scheme * Statutory benefits and above-standard benefits. * VRIM and SGMM * Work-Life Quality Policy (Concilia) NTT offers one of the most comprehensive training programs, focused on 6 core areas covering competencies: -NTT Assets -Soft Skills -Management -Technical -UN -Languages What kind of profile do we seek at NTT? We seek capable individuals with ambition and drive, eager to learn and who embrace the company’s purpose as their own. Minimum academic qualification: Technical Superior University Degree (TSU), Bachelor’s Degree or Engineering degree. * 4 years’ experience as a Tester. * ISTQB * Scrum * DevOps * APIs * Software Testing Methodologies

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

Tester Jr650897291264031224

Tester Jr. At least 1 year of experience in Testing fundamentals, test analysis and design * Degree related to Computer Science. * Minimum 1 year of experience in manual testing. * SQL proficiency. * Agile methodology knowledge is a plus. * Hybrid work arrangement (2 days per week in the office: Thursdays and Fridays; no remote work on those days). Employment type: Full-time Salary: $14,000.00 - $15,000.00 per month Benefits: * Salary increases * Employee discounts * Discounts and preferential pricing * Sick leave days * Medical expense insurance * Major medical expense insurance * Remote work Work location: Hybrid remote in 11520, Granada, CDMX

Lago Margarita 43, Chapultepec Morales, Granada, Miguel Hidalgo, 11520 Ciudad de México, CDMX, Mexico

$MXN 14,000-15,000/year

Manual Tester650897291100181225

Mexico City Manual Tester **Recruiter:**David Reyes **Position:**Manual tester **Location:** CDMX **Industry:** IT, Banking **Work modality:** Hybrid\-Onsite **Your responsibilities:** * Document progress, changes, and key decisions in ALM, as well as extract information from ALM and generate progress reports. * Participate in planning sessions, retrospectives, daily stand\-ups, or follow\-up meetings according to the adopted methodology. * Ensure effective and timely communication with members of involved teams. **Required knowledge and experience:** * ISTQB certification * Agile methodology experience * Executive communication * Risk management * Interaction with users holding positions at the Deputy Director level and above * Availability to attend onsite when required at Patio\-Santa Fe **Skills:** Ability to work under pressure, high work quality, and results\-oriented **Your career at Capgemini** * Working in a team environment, our consultants focus on analyzing, designing, and developing technology\-based solutions for Capgemini’s clients. * You will collaborate with functional, technical, and business specialists to help develop the implementation and integration of innovative solutions and systems, including methodologies, techniques, and tools. * You will contribute responsibly and promptly to customer satisfaction by delivering services and products that generate added value. * Capgemini offers competitive compensation and benefits exceeding statutory requirements. * Our global headquarters are in Paris, France, and we operate in over 50 countries. We have more than 340,000 professionals in Mexico, located in Mexico City, Aguascalientes, and Monterrey. * Capgemini has developed proprietary global methodologies: Collaborative Business Experience and Rightshore. **You’ll love working at Capgemini because:** * We offer a unique recruitment and onboarding experience and support you in building the foundation of your professional career and skills. * We provide a collaborative work environment grounded in our seven core values: Honesty, Boldness, Trust, Freedom, Team Spirit, Modesty, and Fun. * We foster an environment that enables you to plan and develop your career. *“At Capgemini Mexico, our goal is to attract top talent and build a diverse and inclusive workplace; therefore, we do not discriminate based on race, gender, sexual orientation, gender identity or expression, or any other personal characteristic. All applications are welcome and will be considered for selection based solely on candidate merit relative to the job requirements and/or experience. For validation purposes, we will securely use your data—including but not limited to video images or screenshots—during the selection, hiring, and/or onboarding processes. For your security, you may review our privacy notice at:* *https://www.capgemini.com/mx\-es/aviso\-de\-privacidad\-para\-candidatos\-a\-ocupar\-una\-vacante/* Ref. code 392695\-es\_ES Posted on 13 Jan 2026 Experience level Experienced professionals Contract type Permanent Location Mexico City Business unit ABL AMERICAS Brand Capgemini Professional communities Quality Engineering \& Testing

Ópalo Sur 32, Tizayuca, 43806 Tizayuca, Hgo., Mexico

Site Reliability Engineer650897281392671226

Site Reliability Engineer

**Important Information:** * Years of Experience: 5\+ years * Job Mode: Full\-time * Work Mode: Remote within Mexico **Job Summary:** We are seeking a Site Reliability Engineer (19324\) to ensure the reliability, scalability, and performance of custom platforms running on AWS infrastructure and Kubernetes. This role focuses on Tier 3 issue resolution, operational readiness for new releases, and proactive improvements to platform stability and customer experience through SRE best practices. **Responsibilities and Duties:** Troubleshoot and resolve Tier 3 platform issues for AWS\-based custom applications. Collaborate closely with engineering teams to prepare Operations for new releases and feature enhancements. Identify recurring issues and implement automation, tooling, or process improvements to prevent reoccurrence. Design and implement strategies to improve platform reliability, scalability, and performance. Monitor system health and proactively identify risks or degradation. Participate in incident response, root cause analysis, and post\-mortem reviews. Contribute to operational documentation, runbooks, and readiness plans. Partner with internal stakeholders to continuously enhance customer experience and platform robustness. **Qualifications and Skills:** Hands\-on experience supporting and operating AWS cloud environments. Strong knowledge of Kubernetes and container orchestration concepts. Proficiency in Python or Go for automation and scripting. Experience with platform support, troubleshooting, and performance optimization. Familiarity with CI/CD pipelines, monitoring, and observability tools. Strong problem\-solving abilities with an engineering\-focused mindset. **Role\-specific Requirements:** Ability to handle complex production incidents and drive them to resolution. Experience working closely with development teams on operational readiness. Proven ability to identify systemic issues and implement long\-term solutions. Understanding of SRE principles, incident management, and reliability metrics. **Technologies:** AWS, Kubernetes, Docker, Python, Go, CI/CD pipelines, Monitoring and Observability tools, Terraform or CloudFormation (preferred) **Skillset Competencies:** Cloud Infrastructure Management, Container Orchestration, Automation and Scripting, Incident Response, Root Cause Analysis, Reliability Engineering, Cross\-team Collaboration, Documentation and Operational Excellence **About Encora:** Encora is the preferred digital engineering and modernization partner of some of the world's leading enterprises and digital native companies. With over 9,000 experts in 47\+ offices and innovation labs worldwide, Encora's technology practices include Product Engineering \& Development, Cloud Services, Quality Engineering, DevSecOps, Data \& Analytics, Digital Experience, Cybersecurity, and AI \& LLM Engineering. At Encora, we hire professionals based solely on their skills and qualifications, and do not discriminate based on age, disability, religion, gender, sexual orientation, socioeconomic status, or nationality.

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

Test Automation Engineer650896152448021227

Test Automation Engineer

At Cognizant we have an ideal opportunity for you to be part of one of the largest companies in the digital sector worldwide. A Great Place To Work where we look for people who contribute new ideas, experiencing a dynamic and growing environment. At Cognizant we promote an inclusive culture, where we value different perspectives providing career growth and development opportunities. \#WelcomeToCognizant! As a Test Automation Engineer you will play a crucial role in ensuring the quality and reliability of our software products. You will leverage your expertise in automation and scripting to design and execute test plans identify defects and collaborate with cross\-functional teams to enhance product performance. Your contributions will directly impact the companys mission to deliver innovative solutions that improve societal outcomes. Qualifications * Demonstrate proficiency in Automation Desk and vTestStudio for effective test automation. * \+2 years of experience in scripting skills in Python, Bash and CAPL for efficient test execution. * Possess experience in Generative AI to enhance testing capabilities. * Showcase expertise in test framework development to support robust testing processes. * Have a solid understanding of auto\-verification and validation in software testing. ADVANCED ENGLISH IS A MUST Hybrid role in CDMX Responsibilities * Design and implement comprehensive test plans to ensure software quality and performance. * Collaborate with development teams to understand product requirements and create effective test strategies. * Utilize Automation Desk and vTestStudio to automate test cases and streamline testing processes. * Develop and execute scripts using Python Bash and CAPL to perform automated testing and validation. * Apply Generative AI techniques to enhance test coverage and efficiency. * Lead efforts in test framework development to support ongoing testing activities. * Conduct auto\-verification and validation to ensure compliance with industry standards. * Identify document and track defects using established processes and tools. * Provide detailed reports on test results and collaborate with teams to resolve issues. * Participate in code reviews and provide feedback to improve product quality. * Ensure all testing activities are conducted in accordance with company policies and procedures. * Stay updated with the latest testing methodologies and tools to continuously improve testing practices. * Travel as required to collaborate with teams and stakeholders for project success. Why Cognizant? Improve your career in one of the largest and fastest growing IT services providers worldwide Receive ongoing support and funding with training and development plans Have a highly competitive benefits and salary package Get the opportunity to work for leading global companies We are committed to respecting human rights and build a better future by helping your minds and the environment We invest in people and their wellbeing. We create conditions for everyone to thrive. We do not discriminate based on race, religion, color, sex, age, disability, nationality, sexual orientation, gender identity or expression, or for any other reason covered. At Cognizant we believe than our culture make us stronger! Join us now!

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

Vehicle Systems Engineer650896152284171228

Vehicle Systems Engineer

Join our dynamic team as a Test Analyst where you will play a crucial role in ensuring the quality and reliability of automotive systems. With your expertise in diagnostics validation and test plan development you will contribute to the advancement of automotive technology. This position requires a proactive approach to component and system testing ensuring compliance with industry standards. You will collaborate with cross\-functional teams to enhance auto\-verification and validation process **Responsibilities** * Conduct comprehensive diagnostics validation to ensure the accuracy and reliability of automotive systems. * Develop detailed test plans that align with project requirements and industry standards. * Utilize automotive protocols to effectively communicate and troubleshoot system issues. * Implement testing strategies using CANoe and CANalyzer tools to optimize system performance. * Collaborate with engineering teams to integrate dSPACE solutions into testing processes. * Manage test and defect processes to identify and resolve issues efficiently. * Execute component testing to validate individual parts of automotive systems. * Perform system testing to ensure overall functionality and compliance. * Enhance auto\-verification and validation processes to improve system reliability. * Communicate findings and insights to stakeholders to drive informed decision\-making. * Travel as required to support testing activities and collaborate with global teams. * Work from office during day shifts to maintain consistent communication with team members. * Utilize English language skills to document and present test results effectively. **Qualifications** * * Demonstrate proficiency in diagnostics validation and test plan development. * Possess strong knowledge of automotive protocols and testing tools like CANoe and CANalyzer. * Experience with dSPACE solutions is highly desirable. * Familiarity with test and defect management processes is essential. * Expertise in component and system testing is required. * Ability to enhance auto\-verification and validation processes is crucial. * Excellent communication skills in English are mandatory. **Certifications Required** ISTQB Certification Automotive Testing Certification

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

Data Engineer, YouTube Marketing650896151810581229

Data Engineer, YouTube Marketing

Please submit your resume in English \- we can only consider applications submitted in this language. Only applications of candidates with Mexican citizenship will be evaluated for this role in compliance with the provisions of Article 7 of the Federal Labor Law. ### **Minimum qualifications:** * Bachelor's degree or equivalent practical experience. * 3 years of experience in an investigative role (e.g., media analytics, advertising sales, consulting, or financial analysis). * Experience with coding, relational databases, SQL queries, database definitions, and schema design. * Experience designing data pipelines, and dimensional data modeling for synch and asynch system integration and implementation using internal (e.g., Flume, etc.) and external stacks (e.g., DataFlow, Spark, etc.). ### **Preferred qualifications:** * Experience supporting client\-side media and marketing data science. * Experience with big data technologies (e.g., Hadoop, Spark). * Experience in a non\-technical stakeholder\-facing role. * Understanding of incrementality measurement methodologies and frameworks. * Ability to be proactive and flexible to operate in a changing, constantly evolving and collaborative environment. **About the job** ----------------- In this role, you will play a vital role in building and maintaining the data infrastructure that fuels our marketing strategy. You will design, develop, and optimize data pipelines, ensuring data quality and accessibility for advanced analytics. You will enable the marketing team to leverage data\-driven insights to optimize campaigns and measure the impact of marketing initiatives.Know the user. Know the magic. Connect the two. At its core, marketing at Google starts with technology and ends with the user, bringing both together in unconventional ways. Our job is to demonstrate how Google's products solve the world's problems\-from the everyday to the epic, from the mundane to the monumental. And we approach marketing in a way that only Google can\-changing the game, redefining the medium, making the user the priority, and ultimately, letting the technology speak for itself.**Responsibilities** -------------------- * Design, develop, and maintain scalable and reliable data pipelines to collect, process, and store data from various data sources. * Implement data quality checks and monitoring to ensure data accuracy and integrity. * Collaborate with cross\-functional teams (e.g., marketing, data science, engineering, analytics) to understand data requirements and deliver impactful data solutions. * Optimize data infrastructure for performance, efficiency, and scalability to meet evolving business needs. * Create and maintain dashboards and reports to provide actionable insights to the marketing team. Google is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. See also Google's EEO Policy and EEO is the Law. If you have a disability or special need that requires accommodation, please let us know by completing our Accommodations for Applicants form.

Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico

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