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Sr Investigator Management Solutions (IMS) Specialist (budget experience) hybrid CDMX Mexico (Open)65095756166915120

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 36065095756150914121

**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 Mexico65095756134915122

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 Mexico65095756118274123

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)65095756101763124

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 preferred65095756085762125

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.65095756069505126

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 Mexico65095756053122127

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 Based65095756036611128

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

Quality Analyst65095755844865129

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

Electronic Equipment Repair Technician650956366104351210

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 Coordinator650956365628191211

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

Data Steward, Scent650898484811541212

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

Manual Tester650897291100181213

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

Customer Support Team Lead650896149148171214

Customer Support Team Lead

Apollo.io is the leading go\-to\-market solution for revenue teams, trusted by over 500,000 companies and millions of users globally, from rapidly growing startups to some of the world's largest enterprises. Founded in 2015, the company is one of the fastest growing companies in SaaS, raising approximately $250 million to date and valued at $1\.6 billion. Apollo.io provides sales and marketing teams with easy access to verified contact data for over 210 million B2B contacts and 35 million companies worldwide, along with tools to engage and convert these contacts in one unified platform. By helping revenue professionals find the most accurate contact information and automating the outreach process, Apollo.io turns prospects into customers. Apollo raised a series D in 2023 and is backed by top\-tier investors, including Sequoia Capital, Bain Capital Ventures, and more, and counts the former President and COO of Hubspot, JD Sherman, among its board members. As a **Customer Support** **Team Lead**, you will play a critical role in driving the success of our customer support team by coaching and developing representatives, ensuring operational excellence, and fostering a culture of feedback and recognition. You will be responsible for monitoring team performance, implementing coaching plans, and maintaining a deep understanding of our processes and products. This role requires a proactive leader who thrives in a data\-driven environment, excels in cross\-functional collaboration, and is committed to driving both employee and customer success. **Responsibilities** * **2\+ years in a leadership role within customer support or a related field.** * **Prior experience with SaaS, CRM, and telephony tools is a bonus** * **English (Advanced Level Required)** * Contribute to in\-office leadership presence, supporting employees in a hybrid/in\-office environment while maintaining a strong connection with remote teams. * Provide consistent coaching and developmental feedback through weekly 1:1 meetings, ensuring discussions focus on behavioral improvements and performance trends. * Utilize key performance indicators (KPIs) to identify areas for growth and focus discussions on the behaviors driving results. * Document insights from performance inspections and develop action plans to address areas of opportunity. * Plan and lead weekly team meetings in alignment with our company values focusing on team skill development, team\-building, and important business updates. \- Foster a culture of continuous learning through training sessions, mentoring, and career progression planning. * Maintain open lines of communication across teams, providing clear and timely updates on processes, changes, and performance expectations. \- Embody customer obsession by serving as the primary escalation point for unresolved customer issues, ensuring timely and satisfactory resolution. * Actively contribute to cross\-functional projects aimed at enhancing customer experience and driving retention. * Lead by example in ethical decision\-making, fostering inclusivity, fairness, and integrity in all interactions. **Competencies** * Coaching \& Development. Ability to mentor, guide, and upskill employees through structured coaching plans. * Team Engagement \& Motivation. Builds a positive work environment that drives team performance and morale. * Conflict Resolution. Effectively manages disputes, escalations, and difficult conversations with professionalism. * Recognition \& Employee Support – Ensures employees feel valued and supported through structured recognition programs. * KPI Analysis \& Reporting – Proficient in tracking, analyzing, and leveraging performance data (CSAT, AHT, FCR, SLA). * Accountability \& Goal Setting \- Holds employees accountable through coaching, action plans, and performance reviews. * Operational Inspection \& Risk Management – Maintains oversight of business health through proactive inspection processes. * Customer Advocacy – Understands customer needs and ensures support processes align with customer expectations. * Escalation \& Issue Resolution – Quickly identifies customer concerns, escalating when necessary to ensure high\-quality resolutions. * Quality Assurance (QA) \& Continuous Improvement – Uses QA insights to refine support processes and improve service delivery. * Cross\-Functional Collaboration – Works effectively with leadership, HR, product, and other departments. * Stakeholder Management – Ensures clear communication with both local and global teams to align strategies. * Change Management – Clearly communicates new policies, tools, and strategies while securing buy\-in from employees. * Workflow \& Process Optimization – Identifies inefficiencies in support operations and recommends process improvements. * Knowledge Management – Ensures accurate and updated documentation of processes, FAQs, and customer resources. * CRM \& Ticketing Systems (Salesforce, Zendesk, Freshdesk, etc.) – Utilizes customer support tools effectively. \- Data Analytics \& Reporting Tools * Proficient in dashboards and performance tracking platforms. * Crisis Management – Able to quickly assess and resolve operational or customer\-impacting issues. ### **We are AI Native** Apollo.io is an AI\-native company built on a culture of continuous improvement. We’re on the front lines of driving productivity for our customers—and we expect the same mindset from our team. If you're energized by finding smarter, faster ways to get things done using AI and automation, you'll thrive here. ### **Why You’ll Love Working at Apollo** At Apollo, we’re driven by a shared mission: to help our customers unlock their full revenue potential. That’s why we **take extreme ownership** of our work, **move with focus and urgency**, and **learn voraciously** to stay ahead. We invest deeply in your growth, ensuring you have the resources, support, and autonomy to **own your role and make a real impact**. Collaboration is at our core—we’re **all for one**, meaning you’ll have a team across departments ready to help you succeed. We encourage **bold ideas and courageous action**, giving you the freedom to experiment, take smart risks, and drive big wins. If you’re looking for a place where your work matters, where you can push boundaries, and where your career can thrive—Apollo is the place for you.

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

Painter650892599386901215

**PAINTER** Good day, We are a metal-mechanical company that manufactures loading dock levelers, hydraulic systems, excavator cabs for the mining sector, and platform seals. For our painter vacancy, we require at least 6 months of experience in applying vinyl and acrylic paint on metal structures, paint preparation, equipment calibration, and paint leveling. A technical test will be administered. We are offering a gross monthly salary of $11,800.00, plus benefits exceeding statutory requirements. Our location is at Av. Estado de México No. 6, Col. Profesor Cristóbal Higuera, C.P. 52940, Atizapán de Zaragoza. As a reference, we are two blocks from the Red Cross. Shifts: Monday to Friday, 6:00 a.m. to 2:30 p.m.; Saturdays, 6:00 a.m. to 2:30 p.m. Monday to Friday, 2:30 p.m. to 10:00 p.m. Are you interested in scheduling an interview and technical test? What is your name, how old are you, where are you located, and what experience do you have in the metal-mechanical industry?

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

$MXN 11,800/month

MIG Welder650892599224331216

**MIG WELDER** Good day. We are a metal-mechanical company that manufactures hydraulic loading dock levelers, excavator cabins for the mining sector, and platform seals. For the MIG welder position, the salary would be $11,800.00 gross per month, depending on experience, plus $470 in meal vouchers and a 4% savings fund contribution; uniforms are provided free of charge. A technical test must be completed. Candidates must have at least one year of experience welding with solid wire. REQUIREMENTS: * Operation and adjustment of MIG welding equipment. * Operation of manual oxy-cutting and plasma cutting equipment. * Use of various tools (grinder, rotary tool, drill, etc.). * Interpretation of engineering drawings. Benefits we offer include all statutory benefits plus additional ones such as punctuality bonus, meal vouchers, savings fund, and safety equipment provided from day one. Shift Availability: Monday to Friday, 6:00 a.m. to 2:30 p.m.; Saturdays, 6:00 a.m. to 2:00 p.m. Monday to Friday, 2:30 p.m. to 10:00 p.m. We are located in the municipality of Atizapán de Zaragoza, State of Mexico (as a reference, two blocks from the Red Cross). What is your name, how old are you, where are you located, and what experience do you have in the metal-mechanical industry?

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

$MXN 11,800/month

Management System and Certifications Coordinator.650625952087051217

Management System and Certifications Coordinator.

Transportadora Consolidada is looking for your TALENT as a **Management System and Certifications Coordinator**, if you meet all the requirements, do not hesitate to apply. **Requirements:** * Industrial Engineering / Business Administration or related degree * Knowledge of policies and procedures * Quality management * Continuous improvement * Auditing * Mexican Official Standards related to Transportation * ISO 9001:2015, OEA / CTPAT / NORMEX certifications, among others. * Ability to audit departments and present findings * High level of documentary and methodological organization * Analytical ability * Excellent communication skills * Interpersonal skills * Goal-oriented **Responsibilities:** * Maintain the entire Management System up-to-date and valid * Develop the annual internal and external audit plan and ensure its execution * Ensure documentary evidence and traceability * Identify risks and opportunities for improvement in processes * Propose lean improvements, simplification, and automation * Track action plans with responsible parties and deadlines * Prepare all departments for audits * Ensure response times of no more than 72 hours for critical requests * Coordinate continuous improvement plans based on data * Promote operational discipline through evidence * Review processes to simplify and eliminate bureaucracy * Document improvements and ensure their implementation **Work location:** Cuautitlán Izcalli Monday to Friday 8:00 am to 5:00 pm Rotating Saturdays: 8:00 am to 12:00 pm Position type: Full-time Salary: $20,000.00 per month Workplace: On-site employment

C. Lázaro Cárdenas 66, San Francisco Tepojaco, 54745 Cuautitlán Izcalli, Méx., Mexico

$MXN 20,000/year

Analyst - Data Governance650625950156831218

Analyst - Data Governance

As an Analyst \- Data Governance, you are responsible for hands\-on execution and maintenance of our master data and for enforcing policies and processes around data attributes. You will be part of a business\-enabling team that performs day\-to\-day activities around maintaining master data of customer, supplier and product domains. Additionally, you will work with business owners and data management team to help troubleshoot data issues. **Responsibilities:** * Monitors, validates, and executes data create and change requests in data hub in an accurate and timely manner. * Identifies master data exceptions, and further analyze and resolve exceptions with assistance of master data steward. * Conducts data quality audits and compiles issues and impacts for review and action with business. * Performs basic statistical and relational analysis of large data sets to identify and correct inconsistencies. * Executes data cleansing, data enrichment and testing cycles for ERP upgrades and projects. * Participates in governance projects to identify and implement process improvements and increase efficiency. * Enforces data standards to achieve continued data cleanliness. **Qualifications:** * Bachelor’s Degree is required * Technology or Business degree is preferred * 1 year of knowledge of computer system applications: Microsoft Office (E\-mail, Excel and Word), Oracle ERP is required; 2 years preferred. * 1 year of knowledge of data domain and business operations is required: 2 years preferred. * 1 year of skills with data handling and manipulation is preferred. * 1 year of experience with master data management and data tools is preferred. * Able to work independently as well as in a team environment. * Strong written, oral communication, and interpersonal skills with a positive disposition. * Strong attention to detail with a passion for accuracy. * Reliable with strong organizational skills and solution\-oriented philosophy. * Ability to prioritize tasks and demonstrate a willingness to accept new challenges. * Willingness to accommodate temporary working hour changes as required by workflow and deadlines. * Ability to work effectively with all levels of management to accomplish goals and objectives preferred. * Knowledge of project planning and LEAN process improvement preferred At Wesco, we build, connect, power and protect the world. As a leading provider of business\-to\-business distribution, logistics services and supply chain solutions, we create a world that you can depend on. Our Company’s greatest asset is our people. Wesco is committed to fostering a workplace where every individual is respected, valued, and empowered to succeed. We promote a culture that is grounded in teamwork and respect. With a workforce of over 20,000 people worldwide, we embrace the unique perspectives each person brings. Through comprehensive benefits and active community engagement, we create an environment where every team member has the opportunity to thrive. Learn more about Working at Wesco here and apply online today! Founded in 1922 and headquartered in Pittsburgh, Wesco is a publicly traded (NYSE: WCC) FORTUNE 500® company. *Wesco International, Inc., including its subsidiaries and affiliates (“Wesco”) provides equal employment opportunities to all employees and applicants for employment. Employment decisions are made without regard to race, religion, color, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, or other characteristics protected by law. US applicants only, we are an Equal Opportunity Employer.* *Los Angeles Unincorporated County Candidates Only: Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act.*

Perif. Blvd. Manuel Ávila Camacho 3130-piso 7, Valle Dorado, 54020 Tlalnepantla, Méx., Mexico

Principal Technical Support Engineer (Familiar w/ Advanced Process Control)650624856797471219

Principal Technical Support Engineer (Familiar w/ Advanced Process Control)

The driving force behind our success has always been the people of AspenTech. What drives us, is our aspiration, our desire and ambition to keep pushing the envelope, overcoming any hurdle, challenging the status quo to continually find a better way. You will experience these qualities of passion, pride and aspiration in many ways — from a rich set of career development programs to support of community service projects to social events that foster fun and relationship building across our global community. The Role We are seeking a Chemical Engineer to join our Advanced Process Control (APC) team to work as a Principal Technical Support Engineer. The ideal candidate should be able to learn new concepts quickly. The candidate should be an innovative thinker, demonstrate high initiative, have great communication skills and work to the highest ethical standards. Your Impact Troubleshoot \& resolve chemical engineering related industry problems reported by the customer base using AspenTech’s proprietary software Function as a global expert and assist worldwide staff to resolve advanced chemical engineering related industry problems reported by the customer base using AspenTech’s proprietary software Communicate with customers through phone, chat, web\-conferencing, email and in\-person Own escalation of all assigned customer issues and drive holistic resolution cross\-functionally within AspenTech. Work with cross functional management to ensure global issue escalation meets ongoing customer needs. Identify new content areas and lead teams to create technical white papers for publication to AspenTech’s web knowledgebase for areas of expertise Deliver high\-quality advanced level and tailored training classes, which are based on principles of chemical engineering and industrial processes, to industry\-recognized expert users Using expert knowledge of industry trends, lead development of AspenTech’s customer\-facing training materials for new applications and focus in the industry. Mentor others to tailor training materials to specific plants and processes based on customer industrial business needs. Lead a small team functioning as subject matter experts (SME) in AspenTech’s pre\-release beta software testing program to drive improved product quality Lead complex pre\-sales consultations, based on chemical engineering principles and industrial processes, to identify prospects’ business problems and articulate AspenTech’s products as the solution Lead others to architect, configure and deploy AspenTech solutions in customer environments based on customer business needs Conduct health checks on assigned accounts Lead cross\-functional improvement projects as needed with regular updates to an AspenTech management team What You'll Need Bachelor's, Master’s or Ph.D. degree in Chemical Engineering or closely related discipline 6\-10 years of relevant experience. University experience may count. Strong understanding of Chemical Engineering principles with demonstrated expertise Knowledge of Advanced Process Controls is a plus, but not required. Knowledge of chemical and manufacturing business processes in the refining, chemical, pharmaceutical or process industries. Work experience in such an environment is beneficial. Detail\-oriented with hands\-on problem\-solving skills Prior exposure to AspenTech products or competitor tools Strong written and verbal communication skills. Ability to communicate effectively with senior management about business initiatives. Ability to present complex information in a clear and concise manner. Strong customer first mindset, with the ability to identify opportunities that create value for customers Ability to manage multiple responsibilities and competing priorities Ability to travel. Travel is usually less than 25% and may occasionally be international.

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

Electrical Officer650622677902101220

Electrical Officer

**JOIN US AS AN ELECTRICAL OFFICER!** We are a company dedicated to the manufacturing of robotic cells and automated equipment, offering products and services meeting the highest quality standards. **WHAT DO WE LOOK FOR IN AN ELECTRICAL OFFICER?** * Minimum 2–3 years’ experience in installation and maintenance of wiring, control systems, and lighting. * Knowledge of electrical installations, conduit, and cable trays. * Inspection of electrical components and support in activities related to control panel assembly. You will perform testing, installations, and diagnose electrical faults to repair internal or external company wiring, as well as other related equipment or control devices; interpret blueprints; and support activities related to control panel assembly. **KEY SKILLS FOR THIS POSITION** * Strong problem-solving ability. * Ability to work independently and as part of a team. * Commitment to safety and workplace cleanliness. **Education:** Electrical Technician **Salary: $10,000.00–$12,000.00** **Fixed shift of 10 hours (8:00–18:00)** **If interested, contact us via WhatsApp at 5522608471 or apply through this channel by submitting your CV.** Job type: Full-time Salary: $10,000.00–$12,000.00 per month Work location: On-site employment

Adolfo López Mateos 18, San Martin, 54600 Tepotzotlán, Méx., Mexico

$MXN 10,000-12,000/year

Instalador de GPS650622677414431221

Instalador de GPS

TÉCNICO INSTALADOR DE GPS Requisitos: \* Licencia de conducir \* Experiencia mínima de 3 años en instalación de GPS \* Disponibilidad de horario y disponibilidad para viajar Actividades: \* Instalación de: GPS, accesorios como: botón de pánico, paro de motor, sensor de enganche, entre otros. \* Desinstalaciones, revisión de GPS \* Manejo de pruebas de servicios \* Experiencia en sistemas eléctricos de camiones y/o automóviles. \* Capacidad para manejar herramientas \* Capacidad para interpretar diagramas eléctricos. \* Instalación de accesorios automotrices \* Resguardo y control de los equipos asignados para la realización de los servicios. \* Resguardo y buen uso de las herramientas/el equipo celular asignados. \* Emisión oportuna y correcta de las hojas de trabajo realizadas. Aptitudes: \* Compromiso \* Responsabilidad \* Honestidad \* Proactividad \* Actitud de servicio \* Capacidad de respuesta rápida Tipo de puesto: Tiempo completo Sueldo: $12,000\.00 \- $14,000\.00 al mes Beneficios: * Seguro de vida * Uniformes gratuitos * Vales de despensa Lugar de trabajo: Empleo presencial

3J7F+M8 Nantzha, Hgo., Mexico

$MXN 12,000/year

Welding Technician (Official)650622676331531222

Welding Technician (Official)

Job Objective Support the execution of welding and industrial maintenance tasks, ensuring quality, safety, and compliance with the technical standards established by the company. Main Responsibilities * Perform welding tasks on metal structures, pipelines, and industrial components under supervision. * Assist in preparing materials, tools, and welding equipment. * Interpret basic blueprints and technical specifications related to assigned projects. * Comply with industrial safety regulations and proper use of personal protective equipment (PPE). * Collaborate in preventive and corrective maintenance tasks for machinery and structures. * Maintain order and cleanliness in the work area. Working Conditions * Work schedule: Full-time. * Location: Zumpango, State of Mexico. * Contract: Initial probationary period with potential for permanent employment. * Benefits: Statutory benefits, continuous training, and opportunities for growth within the company. Job Type: Full-time, Indefinite-term Salary: Starting at $2,800.00 per week Benefits: * Free uniforms Workplace: On-site employment

Av. Jesus Carranza 9, San Juan, 55600 Zumpango de Ocampo, Méx., Mexico

$MXN 2,800/month

Project Engineer650622675413771223

Project Engineer

Education: Industrial Engineering, PREFERABLY English is essential: fluent conversational level. Skills and knowledge: Fundamentals of IATF16949:2016 standard Knowledge of Core Tools Project Management (Project management and monitoring — Project program monitoring, Direct communication and negotiation with customers and suppliers, Coordination of project follow-up meetings) The position is responsible for assessing the technical feasibility of new projects, coordinating with multidisciplinary teams, customers, and suppliers to validate requirements, proposals, and development viability. It provides comprehensive project follow-up from planning and execution through to release for mass production, ensuring compliance with timelines, activities, and technical specifications. Additionally, it maintains constant communication with customers and suppliers, coordinates testing and validation, participates in the *Safe Launch* phase, and provides internal support to the engineering department. Job type: Full-time, Contract-based Salary: $10,000.00 \- $14,000.00 per month Work location: On-site employment

Calle Av. del Convento S/N, El Trebol, 54614 Tepotzotlán, Méx., Mexico

$MXN 10,000/month

Electromechanical Technician650622674794251224

Electromechanical Technician

**Job Description** Electrician Technician, Industrial Maintenance Technician or Electromechanical Technician Ages 25 to 50 Availability to rotate shifts Industrial maintenance of injection and extrusion machinery and equipment Preventive and corrective maintenance Resident of the Huehuetoca area **Job Type, Category and Subcategory** Electromechanical Technician Indefinite-term employment with probationary period Shift rotation **Qualifications and Skills** Knowledge Electricity Mechanics Hydraulics PLC Temperature and speed control **Benefits** Salary: MXN 14,500.00 Grocery vouchers (10%), Savings Fund (4%) and monthly punctuality bonus Job type: Full-time, Indefinite-term Salary: $14,500.00 – $14,501.00 per month Benefits: * Savings fund * Free parking * Free uniforms * Grocery vouchers Experience: * Maintenance: 3 years (Preferred) Work location: On-site

RQ2J+54 Coyotepec, State of Mexico, Mexico

$MXN 14,500/year

Budget Analyst650622674188831225

**Job Opening: Budget Analyst** **Department:** Financial Reporting **Location:** Big Ben Building, Tlalnepantla, State of Mexico **Monthly Salary:** $12,000 to $13,000 net (depending on experience) **Position Profile:** We are seeking a Budget Analyst with strong analytical skills and solid financial judgment to join our Financial Reporting department. This role is critical for budget planning and monitoring, as well as for analysis supporting strategic decision-making. **Requirements:** * Bachelor’s degree in Accounting, Finance, Business Administration, or related field * Minimum 1 year of experience in financial analysis or budgeting * Intermediate-to-advanced proficiency in Excel (technical test will be administered) * Experience using financial management software and databases * Excellent verbal and written communication skills * High sense of responsibility and confidentiality **Key Skills and Knowledge:** * Financial Analysis: In-depth knowledge of accounting principles and financial analysis tools * Budgeting: Experience in developing, controlling, and monitoring annual budgets, including forecasting * Effective Communication: Ability to present financial information clearly and understandably * IT Tools: Advanced proficiency in spreadsheets, financial software, and databases * Analytical Thinking: Ability to analyze data, identify trends, and formulate recommendations **Benefits and Perks:** * 20-day Christmas bonus * 12 vacation days starting from the first year * 25% vacation premium * 7.5% savings fund * Major medical expense insurance effective from the third month * Grocery vouchers * “Contigo Más” membership with access to telemedicine. **Work Schedule:** Monday to Friday, full-time On-site work at the Big Ben Building, Tlalnepantla. **If you meet the requirements, please send us your updated CV with a photo, including details of your most recent job.** Please note that an **intermediate-to-advanced level of Excel proficiency** is required for this position and will be assessed via a **technical test**. **Thank you for your interest in joining our team! We’re excited to meet you and discover your full potential.** Employment Type: Full-time Salary: $12,000.00 – $13,000.00 per month Benefits: * Complimentary beverages * Savings fund * Grocery vouchers Application Question(s): * How old are you? * How many years of experience do you have in developing and managing annual budgets, including forecasting and monitoring? * How many years of experience do you have applying accounting principles and using financial analysis tools? Experience: * Financial Analysis: 2 years (Mandatory) * Budgeting: 2 years (Mandatory) * Communication Skills: 2 years (Mandatory) * IT Tools Proficiency: 2 years (Mandatory) * Analytical Skills: 2 years (Mandatory) * Microsoft Excel: 4 years (Desirable) Work Location: On-site employment

Av. 30 de Noviembre A, San Andres Atenco, 54040 Tlalnepantla, Méx., Mexico

$MXN 12,000-13,000/year

Repair Technician - Atizapan650521855290901226

Repair Technician - Atizapan

**DIEBOLD NIXDORF DE MEXICO S.A. DE C.V. is seeking a Repair Technician - Atizapan in Atizapán De Zaragoza - Atizapán de Zaragoza, Estado de México** --------------------------------------------------------------------------------------------------------------------------------------------------- **Job Description** Repairs and tests mechanical and electromechanical assemblies and subassemblies. Works from drawings, schematics, wiring diagrams, and written or oral instructions to understand and perform repair and/or test activities. Ensures work complies with established technical, product, and quality requirements. **Responsibilities** * Becomes familiar with field service technician practices and procedures. * Under guidance, performs routine repair technician tasks, including: identifying, isolating, and correcting causes of product malfunction. * Disassembles, cleans, and refurbishes components of assigned products. * Assists with test performance, recordkeeping, and reporting. * Develops working knowledge of Diebold product lines and associated diagnostic and test procedures. * Participates in periodic training on products, repair, and maintenance (on-the-job, classroom, and web-based). * Learns and adheres to DN policies, electrostatic discharge sensitivity, and safety guidelines. * Learns and understands operational manuals, equipment capabilities, and manufacturer instructions. Gains understanding of blueprints, schematics, and electrical diagrams and their use in diagnosing and locating abnormalities. * Provides assistance on special projects assigned. **Qualifications** * Required education or equivalent work experience. * Minimum 0–2 years of relevant experience or equivalent combination of education and experience as a Repair Technician. * Strong written and verbal communication skills. * Experience with mechanical or electromechanical assemblies. * High school diploma or GED or equivalent experience. **Who We Are** *Why join Diebold Nixdorf?* *Brightest minds + technology & innovation + business transformation Diebold Nixdorf people are more than 23,000 teammates with diverse talents and experience across 130+ countries, leveraging future technologies to deliver personalized, secure consumer experiences that connect people with commerce. Our culture is fueled by our values of collaboration, decisiveness, urgency, willingness to change, and accountability.* * *Diebold Nixdorf is an equal opportunity employer and values diversity in our organization. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, gender identity, age, marital status, veteran status, or disability.* *\*\* To all staffing agencies: Diebold Nixdorf does not accept resumes from agencies. Please do not send resumes to our employment alias, to Diebold Nixdorf employees, or to any other location within the organization. Diebold Nixdorf is not responsible for fees related to unsolicited resumes\*\*.* *We are a global company operating across multiple locations and entities. As we aim to find the best solution for our candidates, various legal entities may apply to a job offer. A list of our operating entities can be found here \- \** **Desired Education Level:** Upper Secondary **Desired Experience Level:** Entry Level **Departmental Function:** Maintenance and Repairs **Industry:** Information Services **Skills:** * Attention to Detail * Communication * Sense of Urgency *This job posting originates from the Talenteca.com job board:* *https://www.talenteca.com/anuncio?j\_id\=69626aff3c00004500a2bf91\&source\=indeed*

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

Sheet Metal and Painting Assistant650519013235231227

Sheet Metal and Painting Assistant

**AUTOFIN GROUP INVITES YOU TO JOIN THE TEAM!!!!** JOIN AS: **Sheet Metal and Painting Assistant** **Requirements:** \- Minimum 1 year of experience \- Basic/intermediate knowledge of sheet metal work, painting, polishing, tool handling (technical test required) \- Valid driver's license **We offer:** \* Monthly gross salary of $15,800 + statutory benefits from day one \* Weekly payments \* Schedule: Mon-Fri from 9:00 am to 6:00 pm, and Sat from 9:00 am to 1:00 pm Work location: Perinorte **Interested candidates may apply through this channel or via WhatsApp at 56\-2565\-2941** Job type: Full-time, indefinite term Salary: $15,000\.00 \- $16,000\.00 per month Benefits: * Option for indefinite-term contract Workplace: On-site employment

JR97+X7 Buenavista, State of Mexico, Mexico

$MXN 15,800/year

Mechanical Design Engineer650510406946591228

Mechanical Design Engineer

ALKA MANUFACTURER S.A. DE C.V. is a leading company supplying equipment and services to the automotive industry across three major divisions: marketing, projects, and contract manufacturing; we are seeking: MECHANICAL DESIGN ENGINEER PROFILE: Mechanical Engineer. 1 year of experience as a designer. Valid Class A driver’s license. In-person interviews; SolidWorks test required. EDUCATION/TRAINING: Project development, interpretation and preparation of engineering drawings, product development, mechanical engineering, automotive systems, Microsoft Office suite, SolidWorks, AutoCAD, product costing, cost analysis, FMEA, and ISO 9001:2015 standard. RESPONSIBILITIES: Concept generation. Equipment design. Finite element analysis. Material behavior analysis. Technical drawing for manufacturing processes. Preparation of manufacturing orders. Customer technical support. Component and material analysis. Project management. Technical file management. Field surveys. Assembly supervision. Installation coordination. WORK LOCATION: Tepotzotlán, State of Mexico. Applicant must reside near this area. In-person interview and test attendance is mandatory. WORK HOURS: Monday to Friday, 08:00 to 18:00. WE OFFER: Statutory benefits. Grocery vouchers. Competitive salary. Professional growth opportunities. Employment type: Full-time Salary: $12,400.00 – $15,000.00 per month Employment type: Full-time Benefits: * Option for indefinite-term contract * Grocery vouchers Work schedule: * Monday to Friday Workplace: On-site employment Employment type: Full-time Benefits: * Option for indefinite-term contract * Grocery vouchers Workplace: On-site employment Employment type: Full-time Salary: $12,800.00 – $15,000.00 per month Benefits: * Option for indefinite-term contract * Grocery vouchers Workplace: On-site employment

Av. Insurgentes #26-A, Texcacoa, 54605 Tepotzotlán, Méx., Mexico

$MXN 12,400-15,000/year

Mechanic Assistant650510405397781229

Mechanic Assistant

JOIN ALESSO CUMMINS! We are a company dedicated to the maintenance and distribution of light generators. We are currently seeking: MECHANIC ASSISTANT. Are you looking to develop your career in the mechanical field? WE ARE YOUR OPTION! Requirements: * Knowledge of electro-mechanics * Knowledge and use of mechanical workshop tools * Basic knowledge of diagrams * Basic computer and Microsoft Office skills * Technical degree in diesel mechanics, electronics, or related fields * Availability to travel Activities and knowledge: * Assist technicians in performing equipment inspection and diagnosis. * Assist technicians in diagnosing and repairing faults during corrective and preventive maintenance. * List and quote damaged spare parts for replacement. * Assist in providing general engine repairs. * Complete forms and perform operational tests. We offer: * Statutory benefits * Additional 30 days’ bonus + savings fund + food vouchers + 50% cafeteria support + life insurance * Internal growth opportunities * Ongoing training * Monday to Friday, 8 am to 6 pm, with availability to travel Job type: Full-time Salary: $11,000.00 - $12,000.00 per month Benefits: * Savings fund * Life insurance * Food vouchers Education: * Completed technical degree (Mandatory) Experience: * Diesel mechanics: 1 year (Mandatory) * Standard transmission vehicle operation: 1 year (Mandatory) License/Certification: * Class A driver’s license (Mandatory) Availability to travel: * 75% (Mandatory) Work location: On-site employment

Adolfo López Mateos 18, San Martin, 54600 Tepotzotlán, Méx., Mexico

$MXN 11,000-12,000/year

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