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This role serves as a key point of contact between customers, sales, supply chain, and logistics, contributing to a high level of customer satisfaction while maintaining efficient internal processes.**We kindly request to upload your resume in English.** \n\n \n\n\n\n#### **What you´ll do**\n\n* Accountable for complex decision related to service delivery activities without direct customer interaction; adopt customer centricity mindset.\n* Responsible for automated/manual delivery creation/modification/monitoring (delivery block checks, incomplete deliveries/error logs)\n* Orchestrate/ prioritize customer needs vs. Supply Chain capabilities to fulfill customer/ intercompany orders, while minimizing costs.\n* Contribute to the understanding Voice of Customer/ trends/ needs/ hurdles; support by providing relevant/accurate service delivery info.\n* Enter relevant data in the CRM system to create call plan \\& ensure quality data for business development activities, schedule follow\\-ups.\n* Provide a quality service to customers indirectly, supporting the identification of opportunities to secure new business or support retention.\n* Collaborate closely with internal partners (CSX, CoE, GBS\\+, SC), judging and aligning priorities to meet customer needs vs. SC capabilities.\n* Support the implementation of organizational changes, processes, projects, pilots and regional best practices.\n* Contribute to identifying continuous improvement opportunities to enhance efficiencies, streamline workflows or improve customer experience.\n* Prioritize own workflow, ensure work is completed with productivity, quality \\& timeliness; use KPI's and reports to monitor own performance.\n* Utilize customer service systems and tools (SAP \\& Service Cloud), driving efficiencies and providing feedback to contribute to improvement.\n\n\n#### **What makes you a good fit**\n\n* Bachelor’s degree in Business Administration, Supply Chain, or a related field.\n* 2\\+ years of experience in similar positions.\n* Experience handling purchase orders and customer\\-facing processes is preferred.\n* Basic to intermediate knowledge of SAP and Salesforce; beginner level candidates with strong learning capability are welcome.\n* Understanding of inventory management and shipping processes.\n* Strong organizational skills and attention to detail.\n* Advanced english.\n\n\n#### **Some perks of joining Henkel**\n\n* Flexible work scheme with flexible hours, hybrid work model, and work from anywhere policy for up to 30 days per year\n* Diverse national and international growth opportunities\n* Global wellbeing standards with health and preventive care programs\n* Gender\\-neutral parental leave for a minimum of 8 weeks\n* Employee Share Plan with voluntary investment and Henkel matching shares\n* Flexible Benefits\n* Meal vouchers\n* Savings fund\n* Friday early finish\n\n\nAt Henkel, we come from a broad range of backgrounds, perspectives, and life experiences. We believe the uniqueness of all our employees is the power in us. Become part of the team and bring your uniqueness to us! We welcome all applications across different genders, origins, cultures, religions, sexual orientations, disabilities, and generations.","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768673573624","seoName":"specialist-csx-coe-delivery-enablement","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://mx.ok.com/en/city-ejido-de-san-antonio-tultitlan/cate-testing-quality-assurance/specialist-csx-coe-delivery-enablement-6511021742400112/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"17ef50e4-664b-4a48-b4db-b9cf66f1f668","sid":"e8e77277-0d17-4b4b-b689-c588d1ae8679"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Huixquilucan de Degollado,Estado de México","unit":null}]},"addDate":1768673573624,"categoryName":"Testing & Quality Assurance","postCode":null,"secondCateCode":"info-comm-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"1261,1278,1655","location":"Guanajuato 54, Roma Nte., Cuauhtémoc, 06700 Ciudad de México, CDMX, Mexico","infoId":"6511004819366512","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Supply Chain & Procument Lead","content":"Kapsch is one of Austria's most successful global technology companies. With its comprehensive ITS (Intelligent Transportation Systems) portfolio, Kapsch is actively addressing the challenges of the present and the future with intelligent mobility solutions in a wide range of application areas. As a family\\-owned company founded in 1892 and headquartered in Vienna, Kapsch can look back on 130 years of experience with the future.\n\n**Please attach your CV in English.**\n\n\nWe are looking for a **Supply Chain \\& Procurement Lead** to join our team!\n\n**Your responsibilities:**\n\n* Oversee all logistics operations within the country/Subregion LAM.\n* Analyze statistical data and reports to identify performance trends and drive improvements.\n* Supervise inventory management of materials, goods, and equipment within the country/Subregion LAM.\n* Proactively address performance challenges to support seamless operations.\n* Coordinate transportation and distribution of equipment and materials.\n* Manage material planning efforts with direct oversight of international and local sourcing.\n* Develop and execute a comprehensive supply plan, integrating inputs from demand planning, production capacity, and component availability.\n* Ensure efficient supply chain services, including material planning, scheduling, and strict inventory control for immediate availability.\n* Review purchasing decisions, orders, and contracts to ensure timely fulfillment and resolve discrepancies promptly to maintain quality and company reputation.\n* Conduct and present performance evaluations, including disciplinary actions and performance improvement initiatives.\n* Implement effective inventory control measures to optimize stock levels.\n* Act as the owner of all local supply chain management (SCM) processes and procedures.\n* Ensure compliance with internal and external audits, including legal, environmental, and supplier audits when required.\n\n**Your profile:**\n\n* Previous experience in Procurement/Supply Chain \\& Imports, preferably in IT, construction, telecommunications, energy, or related industries.\n* Advanced English (oral and written).\n* University degree in Business Administration, Supply Chain, or a related field.\n* Key Skills: Proactive mindset, excellent communication, negotiation, and problem\\-solving skills.\n* Proficiency in ERP systems and advanced Office Suite.\n* Willingness to travel within the LAM region when needed.\n\n**Our offer to you:**\n\n* A full\\-time, interesting position within a globally recognized family\\-owned company.\n* Excellent working environment.\n* An international workplace setting.\n* Outstanding benefits.\n\n**Please attach your CV in English.**","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768672251512","seoName":"supply-chain-procument-lead","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://mx.ok.com/en/city-ejido-de-san-antonio-tultitlan/cate-testing-quality-assurance/supply-chain-procument-lead-6511004819366512/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"11985eb2-0ae9-41f2-8854-cb9e82adc656","sid":"e8e77277-0d17-4b4b-b689-c588d1ae8679"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Ciudad de México,Ciudad de México","unit":null}]},"addDate":1768672251512,"categoryName":"Testing & Quality Assurance","postCode":null,"secondCateCode":"info-comm-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"1261,1278,1655","location":"Isabel La Católica 5, Centro Histórico de la Cdad. de México, Centro, Cuauhtémoc, 06000 Ciudad de México, CDMX, Mexico","infoId":"6511004811341012","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Associate Specialist, Logistics Operations","content":"Overview:\n\nThe Associate Specialist, Logistics Operations will execute delivery and logistics activities by transportation mode of packed Goods, liquid or Bulk ensuring on time shipment from the plants/warehouses and on time delivery to the customer. Position will be responsible for day to day SAP transactions in addition to resolving any transportation delays, equipment challenges or other issues impacting on time delivery to the customer.\nResponsibilities:\n* Coordinate all load and shipment processes with local plant / warehouse / terminal personnel and carriers to ensure on time delivery to customer\n* Proactively monitor open orders and deliveries to avoid and resolve issues at the earliest possibility and mitigate negative impact of unavoidable disturbances\n* Key transactional contact for customers and 3rd party logistics service providers\n* Ensure adherence to defined operational escalation process to leads, regional experts and plant personnel when encountering unforeseen delays in shipping from plant and ultimate delivery to customer. 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Integrates subject matter and industry expertise within a defined area. Contributes to standards around which others will operate. Requires in\\-depth understanding of how areas collectively integrate within the sub\\-function as well as coordinate and contribute to the objectives of the entire function. Requires basic commercial awareness. Developed communication and diplomacy skills are required in order to guide, influence and convince others, in particular colleagues in other areas and occasional external customers. Has responsibility for volume, quality, timeliness and delivery of end results of an area. May have responsibility for planning, budgeting and policy formulation within area of expertise. Involved in short\\-term planning resource planning.Full management responsibility of a team, which may include management of people, budget and planning, to include duties such as performance evaluation, compensation, hiring, disciplinary and terminations and may include budget approval. \n\n \n\n**Responsibilities:**\n\n* Develops, enhances, and validates the methods of measuring and analyzing risk, for all risk types including market, credit and operational. Also, may develop, validate and strategize uses of scoring models and scoring model related policies.\n* Manages model risk across the model life\\-cycle including model validation, ongoing performance evaluation and annual model reviews.\n* Produces analytics and reporting used to manage risk for Citi's operations.\n* Translates operational requests from the business into programming and data criteria and conduct systems and operational research in order to model expected results.\n* Assists in the development of analytic engines for business product lines.\n* Communicates results to diverse audiences.\n* Conducts analysis and packages it into detailed technical documentation report for validation purposes sufficient to meet regulatory guidelines and exceed industry standards.\n* Participates on teams to solve business problems.\n* Identifies modeling opportunities that yield measurable business results.\n* Provides guidance to junior validators as and when necessary.\n* Manages stakeholder interaction with model developers and business owners during the model life\\-cycle.\n* Represents the bank in interactions with regulatory agencies, as required.\n* Presents model validation findings to senior management and supervisory authorities.\n* Provides effective challenge to model assumptions, mathematical formulation, and implementation.\n* Assesses and quantifies model risk due to model limitations to inform stakeholders of their risk profile and development of compensating controls.\n* Contributes to strategic, cross\\-functional initiatives within the model risk organization.\n* Full management responsibility of a team, which may include management of people, budget and planning, to include duties such as performance evaluation, compensation, hiring, disciplinary and terminations and may include budget approval.\n* Appropriately assess risk when business decisions are made, demonstrating particular consideration for the firm's reputation and safeguarding Citigroup, its clients and assets, by driving compliance with applicable laws, rules and regulations, adhering to Policy, applying sound ethical judgment regarding personal behavior, conduct and business practices, and escalating, managing and reporting control issues with transparency, as well as effectively supervise the activity of others and create accountability with those who fail to maintain these standards.\n\n**Qualifications:**\n\n* 6\\-10 years experience\n* Consistently demonstrates clear and concise written and verbal communication skills\n* Self\\-motivated and detail oriented\n* Demonstrated project management and organizational skills and capability to handle multiple projects at one time .\n* Practical experience using SAS or similar statistical coding software to build and test prediction models. comfortable interfacing with business clients. proficiency handling very large data sets.\n* Experience in a quantitative role in risk management at a financial institution with experience in either model development or validation.\n* Good knowledge and understanding of a variety of model development and validation testing techniques covering risk models.\n\n**Education:**\n\n* Bachelor’s/University degree or equivalent experience, potentially Masters degree\n\n**Job description**\n\n* Ensure that models in use have undergone appropriate validation and approval processes, promptly identify new or changed models, and provide all necessary information for validation activities.\n* Collaborate with Model Developers in the development of new scoring models as per business requirement. 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We combine expert legal support with intelligent automation, transforming how transactional law is delivered.\n\n\nWe’re not a traditional law firm. We are a diverse and globally distributed team of lawyers, engineers, and innovators working across the U.S, EMEA, and APAC. We believe technology augments, not replaces legal expertise. 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Education: Technical degree in Emergency Medical Services, Paramedicine, Nursing, or related field (preferred but not mandatory).\n\nExperience:\n\n* Coordination of services or direct patient care.\n* Experience in cash handling (billing) and medical test quotation is preferred.\n\nKnowledge:\n\n* Basic pre-hospital care and patient transfer assistance (preferred).\n* Basic laboratory/imaging and mobile services processes.\n* Proficiency in scheduling, data entry, and billing systems.\n\nSkills:\n\n* Organization and planning.\n* Ability to respond effectively in emergencies.\n* Clear and empathetic communication.\n* Direct interaction with patients and clients.\n\n**Personal Competencies**\n\n* Proactivity and accountability.\n* Results- and service-oriented mindset.\n* Teamwork and collaboration.\n* Problem-solving under pressure.\n* Commitment to patient quality and safety.\n\n**We Offer**\n\n* Competitive salary commensurate with the position.\n* Job stability.\n* Initial and ongoing training on patient care protocols, billing, and quotation procedures.\n* Opportunities for career growth within the organization.\n\nEmployment Type: Full-time, Indefinite-term contract\n\nSalary: $10,046.52 – $12,295.68 per month\n\nBenefits:\n\n* Salary increases\n* Savings fund\n* Employee discount\n* Gym discount\n* Discounts and preferential pricing\n* Paternity leave exceeding statutory requirements\n* Company parking\n* Free parking\n* Flexible working hours\n* Option for indefinite-term contract\n* Cafeteria service\n* Gym service\n* Company phone\n\nWork Location: On-site employment","price":"$MXN 10,046-12,295/year","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768560596607","seoName":"Coordinador+de+servicios+m%C3%B3viles+Turno+Nocturno","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://mx.ok.com/en/city-ejido-de-san-antonio-tultitlan/cate-testing-quality-assurance/coordinador%2Bde%2Bservicios%2Bm%25c3%25b3viles%2Bturno%2Bnocturno-6509575636569712/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"1c8144cc-f4f7-4396-8da9-ea0ad2558213","sid":"e8e77277-0d17-4b4b-b689-c588d1ae8679"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace 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Reolín Barejon 21, La Estacion, 52006 Lerma de Villada, Méx., Mexico","infoId":"6509575621760312","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Quality Auditor","content":"**QUALITY AUDITOR POSITION (AUTOMOTIVE)** \n\n**DUE TO PRODUCTION INCREASE**\n\n**Publication Date:** January 15, 2026 \n**Salary:** 9,000 (MXN) \\- 10,000\\.00 (MXN) per month\n\n**Job Description:** \nWe are seeking QUALITY AUDITORS due to increased production at an automotive company located in Lerma, Parque Litos (across from Plaza Sendero). \nNext to the security booth, please drop your job application in the mailbox and/or provide your details through this channel. INTERVIEWS ONLY. THANK YOU! \nRequirements:\n\n* High school diploma or technical degree\n* Availability to work rotating shifts\n* Proven experience as a quality auditor in an industrial manufacturing company, preferably automotive. Key responsibilities include: initiating first-defect stoppage upon identifying non-compliance with Quality Management System standards; identifying non-conformities versus defined standards; labeling NOK parts; completing QRAP forms; identifying customer complaints; complying with Valeo’s standard requirements.\n\nWe offer:\n\n* Benefits exceeding legal requirements (transportation, cafeteria, year-end bonus, savings fund, grocery vouchers, career progression by category, educational assistance, etc.)\n* Available transportation routes: Colinas del Sol, Ameyalco, Zinacantepec\n* Communities served: Almoloya de Juárez, Santiago Miltepec, San Cristóbal H., San Andrés C., El Cerrillo, San Miguel Ameyalco, San Mateo Atenco, San Juan de las Huertas, San Antonio Acahualco, San Luis Mextepec, Seminario, Toluca, Metepec.\n\n*\\- At Valeo, we comply with current labor laws and are committed to fostering a culture of belonging by hiring talent based on competencies, skills, and potential; we do not discriminate for any reason, including gender, age, ethnic origin, physical appearance, marital status, health conditions due to any illness, socioeconomic status, disability, sexual orientation, gender identity or expression; therefore, during the recruitment process, we will not request personal information.*\n\n*\\- At Valeo, we commit to ensuring that our employees enjoy, day after day, a respectful workplace, free from discrimination and sexual harassment, as stipulated in our Global Code of Ethics and Business Conduct.*\n\n\\-*By complying with labor legislation, our recruitment process incurs no cost to applicants and/or candidates. Thus, under no circumstances will we ask you to deliver, deposit, or transfer money or any other resource.*\n\n\\-*If you require specific accommodations during the recruitment process, please inform the recruiter at the outset.* \n*Thank you for your attention*\n\nJob Type: Full-time \nBenefits:\n\n* Salary increases\n* Transportation assistance or service\n* Paternity leave exceeding statutory requirements\n* Company parking\n* Life insurance\n* Cafeteria service\n* Grocery vouchers\n\nWork Location: On-site employment\n\nJob Type: Full-time\n\nSalary: $9,000\\.00 \\- $10,000\\.00 per month\n\nBenefits:\n\n* Transportation assistance or service\n* Company parking\n* Free parking\n* Life insurance\n* Cafeteria service\n* Free uniforms\n* Grocery vouchers\n\nWork Location: On-site employment","price":"$MXN 9,000-10,000/month","unit":"per month","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768560595450","seoName":"quality-auditor","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://mx.ok.com/en/city-ejido-de-san-antonio-tultitlan/cate-testing-quality-assurance/quality-auditor-6509575621760312/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"d11f7fa4-488a-4f3d-aa43-4594e3cb1ce3","sid":"e8e77277-0d17-4b4b-b689-c588d1ae8679"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Lerma de Villada,Estado de México","unit":null}]},"addDate":1768560595450,"categoryName":"Testing & Quality Assurance","postCode":null,"secondCateCode":"info-comm-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"1261,1278,1655","location":"Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico","infoId":"6509575616691512","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Sr Investigator Management Solutions (IMS) Specialist (budget experience) hybrid CDMX Mexico (Open)","content":"**Updated:** January 7, 2026 \n\n**Location:** Tlalnepantla, MEX, Mexico \n\n**Job ID:** 25104568\n\n\nNot ready to apply? \n\nJoin our Talent Network\n**Description**\n\n\nSr Investigator Management Solutions (IMS) Specialist (budget experience) hybrid CDMX Mexico (Open)\nSyneos 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.\n\n\nOur 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.\n\n\nWhether 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.\n\n\nDiscover what our 29,000 employees, across 110 countries already know:\n\n**WORK HERE MATTERS EVERYWHERE**\n\n\nWhy Syneos Health\n\n* 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.\n* 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.\n* 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.\n\n**Job Responsibilities**\n\n\nJOB SUMMARY \n\nThe IMS Budget Specialist I plays an important role to the Clinical Development Services team. As the \n\nliaison between Operations Management, Site Contracts, Clinical Operations, Investigator Management \n\nSolutions Payments Team, the IMS Budget Specialist I will provide analytical insight and support \n\nreviewing site budgets, study protocols, and ensuring alignment within the dedicated clinical trial \n\nmanagement system. \n\nJOB RESPONSIBILITIES \n\n Analyzes and interprets the payment terms and conditions of fully executed site clinical trial \n\nagreement (CTA). \n\n Ensures accuracy of contract budget \\& clinical trial management system (CTMS) template alignment. \n\n Inputs site budget cost utilizing the templates within CTMS. \n\n Engages project team with the quality control of the cost structure created within CTMS. \n\n Serves as subject matter expert for department and project teams concerning contract interpretation \n\nand development of payment strategy. \n\n Ensures the presence of required vendor financial account details participating in clinical trial. \n\n Ensures acquisition and completeness of tax related documentation. \n\n Participates in payment setup issue resolution. \n\n Liaises with internal departments including the Operations, Finance, and Legal teams. \n\n Performs a variety of administrative functions, updates and maintains setup details and progress \n\nstatus of contractual site budgets in the database, and other related duties as assigned. \n\n Works with enterprise financial systems. \n\n Ability to multi\\-task on several projects.\n\n\nPossess strong communication skills and be an effective team player. \n\n Proactively participates in Investigator Payment Planning (IPP) Meetings, providing input to payment \n\nstrategy planning for incoming studies. \n\n Minimal travel may be required (up to 25%). \n\nQUALIFICATION REQUIREMENTS (please indicate if ‘preferred’) \n\n Bachelor’s degree, or equivalent education and experience, plus minimal experience in contract \n\nadministration or finance. \n\n Requires strong communication, verbal, written, and interpersonal. \n\n Ability to build team relationships with line management, employees, and HR team. \n\n Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), email, and voicemail. \n\n Ability to interact and build relationships with all levels of employees. \n\n Ability to organize and prioritize work to meet frequent deadlines is essential. \n\n Strong customer services skills and ability to maintain confidentiality.\n\n**Get to know Syneos Health**\n\n \n\nOver 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.\n\n\nNo 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.\n\n\nhttp://www.syneoshealth.com\n\n**Additional Information**\n\n \n\nTasks, 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.","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768560595054","seoName":"senior-investigator-management-solutions-specialist-budget-experience-hybrid-cdmx-mexico-open","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://mx.ok.com/en/city-ejido-de-san-antonio-tultitlan/cate-testing-quality-assurance/senior-investigator-management-solutions-specialist-budget-experience-hybrid-cdmx-mexico-open-6509575616691512/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"e70da18c-8f1f-4547-a531-47ec43d0145e","sid":"e8e77277-0d17-4b4b-b689-c588d1ae8679"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Tlalnepantla,Estado de México","unit":null}]},"addDate":1768560595054,"categoryName":"Testing & Quality Assurance","postCode":null,"secondCateCode":"info-comm-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"1261,1278,1655","location":"Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico","infoId":"6509575615091412","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Mgr, FSP 360","content":"**Updated:** January 7, 2026 \n\n**Location:** Tlalnepantla, MEX, Mexico \n\n**Job ID:** 25104647\n\n\nNot ready to apply? \n\nJoin our Talent Network\n**Description**\n\n\nMgr, FSP 360\nSyneos 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.\n\n\nOur 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.\n\n\nWhether 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.\n\n\nDiscover what our 29,000 employees, across 110 countries already know:\n\n**WORK HERE MATTERS EVERYWHERE**\n\n\nWhy Syneos Health\n\n* 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.\n* 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.\n* 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.\n\n**Job Responsibilities**\n\n**Overall, the role will be responsible for three primary performance areas:**\n\n**1\\) Customer Delivery and Success**\n\n* 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.\n* 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.\n* 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.\n* Proactively communicates and manages customer issues through assigned escalation channels.\n* 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.\n* Conducts oversight visits as required for Clinical Research Associates.\n* Responsible for all system updates, and compliance with systems and relevant procedure and practices applicable to the customer and Syneos Health processes.\n\n**2\\) Business Impact**\n\n* 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.\n* 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.\n* May serve as a Company representative at professional meetings or seminars.\n\n\n3\\) **People Leadership**\n\n* Responsible for active management of team members’ performance through the established Syneos Health process; at an individual contributor level.\n* Verifies that team members adhere to training guidelines, maintain their training records and individual and corporate training needs are identified and addressed.\n* Provides administrative oversight (for example, HR processes, timecards, expense reports).\n* Supports team members’ professional development through coaching, providing opportunities to increase knowledge and skill levels, and by delegating tasks commensurate with skill level.\n* Proactively works to ensure team members’ engagement, retention and turnover rates remain within expected levels.\n* Demonstrates commitment to diversity, equity, and inclusion through continuous development of all staff, modeling inclusive behaviors and proactively managing bias.\n\n**Get to know Syneos Health**\n\n \n\nOver 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.\n\n\nNo 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.\n\n\nhttp://www.syneoshealth.com\n\n**Additional Information**\n\n \n\nTasks, 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.\n\n**Summary**\n\n\nResponsible 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.","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768560594929","seoName":"Mgr%2C+FSP+360","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://mx.ok.com/en/city-ejido-de-san-antonio-tultitlan/cate-testing-quality-assurance/mgr%252c%2Bfsp%2B360-6509575615091412/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"2f51af6d-300f-4c29-bc0e-db8f908f4897","sid":"e8e77277-0d17-4b4b-b689-c588d1ae8679"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Tlalnepantla,Estado de México","unit":null}]},"addDate":1768560594929,"categoryName":"Testing & Quality Assurance","postCode":null,"secondCateCode":"info-comm-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"1261,1278,1655","location":"Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico","infoId":"6509575613491512","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Safety & PV Specialist I or II (CPQA & medical devices experience) Home Based Mexico","content":"**Updated:** January 7, 2026 \n\n**Location:** Tlalnepantla, MEX, Mexico \n\n**Job ID:** 25104865\n\n\nNot ready to apply? \n\nJoin our Talent Network\n**Description**\n\n\nSafety \\& PV Specialist I or II (CPQA \\& medical devices experience) Home Based Mexico\nSyneos 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.\n\n\nOur 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.\n\n\nWhether 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.\n\n\nDiscover what our 29,000 employees, across 110 countries already know:\n\n**WORK HERE MATTERS EVERYWHERE**\n\n\nWhy Syneos Health\n\n* 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.\n* 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.\n* 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.\n\n**Job Responsibilities**\n\n* 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.\n* Maintains safety tracking for assigned activities.\n* Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, MedDRA coding as required.\n* Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA.\n* Manual recoding of un\\-recoded product and substance terms arises from ICSRs.\n* Identification and management of duplicate ICSRs.\n* Activities related to SPOR / IDMP.\n* Quality review of ICSRs.\n* 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.\n* 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.\n* Fosters constructive and professional working relationships with all project team members, internal and external.\n* Participates in audits as required/appropriate.\n* Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities.\n\n\nQualifications:\n\n* 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.\n* Safety Database systems and knowledge of medical terminology required.\n* 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.\n* Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), Visio, email (Outlook), Team Share (or another management/shared content/workspace) and internet.\n* Ability to work independently and in a team environment.\n* Excellent communication and interpersonal skills, both written and spoken.\n* Good organizational skills with proven ability to prioritize and work on multiple tasks and projects.\n* Detail oriented with a high degree of accuracy and ability to meet deadlines.\n\n**Get to know Syneos Health**\n\n \n\nOver 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.\n\n\nNo 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.\n\n\nhttp://www.syneoshealth.com\n\n**Additional Information**\n\n \n\nTasks, 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.\n\n**Summary**\n\n\nRoles 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.","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768560594803","seoName":"Safety+%26+PV+Specialist+I+or+II+%28CPQA+%26+medical+devices+experience%29+Home+Based+Mexico","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://mx.ok.com/en/city-ejido-de-san-antonio-tultitlan/cate-testing-quality-assurance/safety%2B%2526%2Bpv%2Bspecialist%2Bi%2Bor%2Bii%2B%2528cpqa%2B%2526%2Bmedical%2Bdevices%2Bexperience%2529%2Bhome%2Bbased%2Bmexico-6509575613491512/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"f3e82f3a-949d-41f5-9cdd-5607250a61b9","sid":"e8e77277-0d17-4b4b-b689-c588d1ae8679"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Tlalnepantla,Estado de México","unit":null}]},"addDate":1768560594803,"categoryName":"Testing & Quality Assurance","postCode":null,"secondCateCode":"info-comm-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"1261,1278,1655","location":"Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico","infoId":"6509575611827412","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Safety & PV Specialist (case processing) Hybrid Mexico","content":"**Updated:** December 4, 2025 \n\n**Location:** Tlalnepantla, MEX, Mexico \n\n**Job ID:** 25103060\n\n\nNot ready to apply? \n\nJoin our Talent Network\n**Description**\n\n\nSafety \\& PV Specialist (case processing) Hybrid Mexico\nSyneos 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.\n\n\nOur 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.\n\n\nWhether 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.\n\n\nDiscover what our 29,000 employees, across 110 countries already know:\n\n**WORK HERE MATTERS EVERYWHERE**\n\n\nWhy Syneos Health\n\n* 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.\n* 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.\n* 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.\n\n**Job Responsibilities**\n\n* 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.\n* Maintains safety tracking for assigned activities.\n* Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, MedDRA coding as required.\n* Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA.\n* Manual recoding of un\\-recoded product and substance terms arises from ICSRs.\n* Identification and management of duplicate ICSRs.\n* Activities related to SPOR / IDMP.\n* Quality review of ICSRs.\n* 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.\n* 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.\n* Fosters constructive and professional working relationships with all project team members, internal and external.\n* Participates in audits as required/appropriate.\n* Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities.\n\n\nQualifications:\n\n* 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.\n* Safety Database systems and knowledge of medical terminology required.\n* 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.\n* Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), Visio, email (Outlook), Team Share (or another management/shared content/workspace) and internet.\n* Ability to work independently and in a team environment.\n* Excellent communication and interpersonal skills, both written and spoken.\n* Good organizational skills with proven ability to prioritize and work on multiple tasks and projects.\n* Detail oriented with a high degree of accuracy and ability to meet deadlines.\n\n**Get to know Syneos Health**\n\n \n\nOver 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.\n\n\nNo 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.\n\n\nhttp://www.syneoshealth.com\n\n**Additional Information**\n\n \n\nTasks, 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.\n\n**Summary**\n\n\nRoles 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.","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768560594673","seoName":"safety-pv-specialist-case-processing-hybrid-mexico","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://mx.ok.com/en/city-ejido-de-san-antonio-tultitlan/cate-testing-quality-assurance/safety-pv-specialist-case-processing-hybrid-mexico-6509575611827412/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"bd6a1599-8d10-4d08-9377-9dbe99a1287d","sid":"e8e77277-0d17-4b4b-b689-c588d1ae8679"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Tlalnepantla,Estado de México","unit":null}]},"addDate":1768560594673,"categoryName":"Testing & Quality Assurance","postCode":null,"secondCateCode":"info-comm-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"1261,1278,1655","location":"Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico","infoId":"6509575610176312","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Sr Clinical Data Scientist CDM (Hybrid -ARG & MEX Only)","content":"**Updated:** December 16, 2025 \n\n**Location:** Tlalnepantla, MEX, Mexico \n\n**Job ID:** 25102142\\-OTHLOC\\-7304\\-2DH\n\n\nNot ready to apply? \n\nJoin our Talent Network\n**Description**\n\n\nSr Clinical Data Scientist CDM (Hybrid \\-ARG \\& MEX Only)\nSyneos 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.\n\n\nOur 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.\n\n\nWhether 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.\n\n\nDiscover what our 29,000 employees, across 110 countries already know:\n\n**WORK HERE MATTERS EVERYWHERE**\n\n\nWhy Syneos Health\n\n* 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.\n* 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.\n* 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.\n\n**Job Responsibilities**\n\n\n\\*\\*\\*This role is only open to hiring in Argentina and Mexico. Hybrid \\- 2 days in office per week (Buenos Aires and Mexico City)\n\n\n\\*\\*\\*Proficiency in English is required \\- Please submit CVs in English.\n\n\n\\*\\*\\*Previous experience within Veeva Vault is required.\n\n* \n\n\nServes 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* \n\n\nActs 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* \n\n\nEnsures the required data elements and corresponding data quality oversight steps are identified to support the defined study analysis* \n\n\nWorks 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* \n\n\nCoordinates 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* \n\n\nDrives 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.* \n\n\nDrives 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* \n\n\nMonitors and communicates project progress to the Sponsor and project team including use of project status reports and tracking tools/metrics* \n\n\nEnsures 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* \n\n\nReview, maintain budget and identify out of scope for Clinical Sciences activities, raise to PM to be implemented in required change order* \n\n\nPlans, manages, and requests Clinical Data Science resources for assigned projects* \n\n\nCoordinates the work of the assigned Clinical Data Science team* \n\n\nDevelops and maintains project plans, specifications, and documentation in line with SOP requirements* \n\n\nMaintains documentation on an ongoing basis and ensures that all TMF filing is up to date for necessary files* \n\n\nParticipates in, and presents at internal, Sponsor, third\\-party, and investigator meetings on behalf of clinical data science responsibilities* \n\n\nPrepares input, and participates in proposal bid defense meetings and request for proposals on behalf of clinical data science responsibilities* \n\n\nPlans for and creates necessary documentation to support internal and external audits; participates in such audits on behalf of clinical data sciences responsibilities* \n\n\nTrains and mentors new or junior team members* \n\n\nMaintains proficiency in Clinical Data Science systems and processes through regular training. May attend/represent the company at professional meetings/conferences* \n\n\nPerforms other work\\-related duties as assigned. Minimal travel may be required (up to 25%)**Get to know Syneos Health**\n\n \n\nOver 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.\n\n\nNo 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.\n\n\nhttp://www.syneoshealth.com\n\n**Additional Information**\n\n \n\nTasks, 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.\n\n**Summary**\n\n\nResponsible 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.","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768560594545","seoName":"Sr+Clinical+Data+Scientist+CDM+%28Hybrid+-ARG+%26+MEX+Only%29","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://mx.ok.com/en/city-ejido-de-san-antonio-tultitlan/cate-testing-quality-assurance/sr%2Bclinical%2Bdata%2Bscientist%2Bcdm%2B%2528hybrid%2B-arg%2B%2526%2Bmex%2Bonly%2529-6509575610176312/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"401feee6-db0c-49b0-9cf9-629dc70a799a","sid":"e8e77277-0d17-4b4b-b689-c588d1ae8679"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Tlalnepantla,Estado de México","unit":null}]},"addDate":1768560594545,"categoryName":"Testing & Quality Assurance","postCode":null,"secondCateCode":"info-comm-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"1261,1278,1655","location":"Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico","infoId":"6509575608576212","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"CSR Appendices Coordinator - RIMS System Exp preferred","content":"**Updated:** January 10, 2026 \n\n**Location:** Tlalnepantla, MEX, Mexico \n\n**Job ID:** 25103128\\-OTHLOC\\-7302\\-2DR\n\n\nNot ready to apply? \n\nJoin our Talent Network\n**Description**\n\n\nCSR Appendices Coordinator \\- RIMS System Exp preferred\nSyneos 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.\n\n\nOur 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.\n\n\nWhether 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.\n\n\nDiscover what our 29,000 employees, across 110 countries already know:\n\n**WORK HERE MATTERS EVERYWHERE**\n\n\nWhy Syneos Health\n\n* 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.\n* 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.\n* 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.\n\n**Job Responsibilities**\n\n**Roles and Responsibilities:**\n\n* 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).\n* 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.\n* Effectively communicates deliverables needed to stakeholders. Must demonstrate good interpersonal and organizational communication skills, including conflict management skills.\n* Effectively attends to multiple tasks within overlapping timeframes; builds positive and productive relationships that enable high quality documents to be completed on time.\n\n**Get to know Syneos Health**\n\n \n\nOver 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.\n\n\nNo 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.\n\n\nhttp://www.syneoshealth.com\n\n**Additional Information**\n\n \n\nTasks, 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.\n\n**Summary**\n\n\nResponsible for authoring of Clinical Study Report (CSR) Appendices and managing clinical and regulatory references.","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768560594419","seoName":"CSR+Appendices+Coordinator+-+RIMS+System+Exp+preferred","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://mx.ok.com/en/city-ejido-de-san-antonio-tultitlan/cate-testing-quality-assurance/csr%2Bappendices%2Bcoordinator%2B-%2Brims%2Bsystem%2Bexp%2Bpreferred-6509575608576212/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"84e4dcda-bc96-45d8-ae94-61829bcaa6c7","sid":"e8e77277-0d17-4b4b-b689-c588d1ae8679"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Tlalnepantla,Estado de México","unit":null}]},"addDate":1768560594419,"categoryName":"Testing & Quality Assurance","postCode":null,"secondCateCode":"info-comm-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"1261,1278,1655","location":"Sindicato Nacional de Electricistas 54, Hab Viveros del Valle, 54060 Tlalnepantla, Méx., Mexico","infoId":"6509575606950512","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Safety & PV Specialist II - MXN Office Based - Exp in Mailbox Mgmt & All Report Processing would be preferred.","content":"**Updated:** December 3, 2025 \n\n**Location:** Tlalnepantla, MEX, Mexico \n\n**Job ID:** 25102866\n\n\nNot ready to apply? \n\nJoin our Talent Network\n**Description**\n\n\nSafety \\& PV Specialist II \\- MXN Office Based \\- Exp in Mailbox Mgmt \\& All Report Processing would be preferred.\nSyneos 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.\n\n\nOur 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.\n\n\nWhether 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.\n\n\nDiscover what our 29,000 employees, across 110 countries already know:\n\n**WORK HERE MATTERS EVERYWHERE**\n\n\nWhy Syneos Health\n\n* 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.\n* 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.\n* 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.\n\n**Job Responsibilities**\n\n\nJob Description* Enters information into PVG quality and tracking systems for receipt and tracking ICSR as required.\n* May assist in the preparation of the project plans such as Safety Management Plan.\n* May perform set\\-up, delivery and close\\-out of safety and pharmacovigilance projects.\n* Processes ICSRs according to Standard Operating Procedures (SOPs) and project/program\\-specific safety plans.\n* Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability.\n* Enters data into safety database.\n* Codes events, medical history, concomitant medications, and tests.\n* Compiles complete narrative summaries.\n* Assesses information to be queried and follows up until information is obtained and queries are satisfactorily resolved.\n* Participates in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements.\n* Coordinates with data management staff concerning reconciliation of safety data between the clinical and safety databases.\n* Maintains safety tracking for assigned activities.\n* Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, and MedDRA coding as required.\n* Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA.\n* Manual recoding of un\\-recoded product and substance terms arises from ICSRs.\n* Identification and management of duplicate ICSRs.\n* Activities related to SPOR / IDMP.\n* Quality review of ICSRs.\n* Quality review for the work performed by peers.\n* Serves as a subject matter expert in SPVG, which includes resolution of project related routine queries; mentoring, coaching, and training of new hires.\n* Fosters constructive and professional working relationships with all project team members, internal and external.\n* Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities.\n* 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.\n* Participate in audits/inspections as required.\n* 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.\n* 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.\n**Get to know Syneos Health**\n\n \n\nOver 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.\n\n\nNo 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.\n\n\nhttp://www.syneoshealth.com\n\n**Additional Information**\n\n \n\nTasks, 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.\n\n**Summary**\n\n\nJob 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. 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