[Skip to main content](#main-content) [OpenNash Jobs](https://jobs.opennash.com/) [Hiring report](/reports/hiring/) · [All Abbott Laboratories jobs](https://jobs.opennash.com/companies/abbott-laboratories/) · [Search jobs](/search/) Abbott Laboratories # Sr. Regulatory Affairs Specialist- Diabete-Rungis H/F Full-time Senior individual contributor Legal & Compliance Listed on Abbott Laboratories’s official careers site. Posted October 14, 2026. Check that it is still open and apply there. [Apply on Abbott Laboratories’s careers site →](https://abbott.wd5.myworkdayjobs.com/abbottcareers/job/France--Rungis--Miami-Building/Sr-Regulatory-Affairs-Specialist--Diabete-Rungis-H-F_31164356) [OpenNash Jobs](https://jobs.opennash.com/) / [Abbott Laboratories](https://jobs.opennash.com/companies/abbott-laboratories/) / Sr. Regulatory Affairs Specialist- Diabete-Rungis H/F ## Job description ### JOB DESCRIPTION About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to: Career development with an international company where you can grow the career you dream of. A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. About the Role This position works out of our France, Rungis location in the Abbott Diabetes Care (ADC) Division. We are seeking a highly skilled Regulatory Affairs Sr. Specialist to join Abbott Diabetes Care and lead regulatory activities across the EMEAP region, with a focus on France. In this role, you will drive regulatory strategy, ensure compliance with global and local requirements, and support the timely introduction and lifecycle management of innovative diabetes care products. You will collaborate closely with cross‑functional teams including Global Regulatory, R&D, Quality, Market Access, Marketing, Sales, Government Affairs, and Legal. This position is ideal for a proactive, detail‑oriented regulatory professional who thrives in a matrixed, international environment. ### What You’ll Do Lead and manage regulatory activities for new product launches and rollouts across EMEAP Prepare, review, and maintain high‑quality technical documentation, including CE‑marking files for medical devices and IVDs. Support in‑country regulatory submissions, notifications, registrations, reimbursement activities, and tender documentation. Provide regulatory guidance for marketing materials and promotional activities. Monitor, interpret, and communicate regulatory intelligence for assigned countries. Advise internal teams on MDR, IVDR, and local regulatory requirements; support implementation of new or updated regulations. Coordinate regulatory strategy for design or labeling changes, including documentation review and authority interactions. Participate in internal and external audits with regulatory impact. Ensure compliance with Abbott’s Quality System, ISO 13485, MDR/IVDR, and applicable local regulations. Build and maintain strong relationships with regulatory authorities and internal stakeholders. Contribute to projects improving quality system efficiency and product quality. ### Required Qualifications Min. Bachelor’s degree in a scientific discipline. Solid understanding of MDR (EU 2017/745) requirements, including the CE‑marking process, and applicable regulatory frameworks to Medical Devices; experience with In Vitro Diagnostics (IVDs) is preferred. Min 5 years experience in a similar regulatory affairs role. Experience with in‑country regulatory activities in France Proven ability to lead regulatory strategy for product launches, design changes, and labeling updates. Strong organizational skills and ability to work effectively in a matrixed, geographically diverse environment. Excellent communication skills in English and French, both written and verbal (Knowledge of other languages would be an advantage). Experience interacting with regulatory authorities and supporting cross‑functional teams (R&D, Quality, Market Access, Marketing, Sales). The base pay for this position is N/A In specific locations, the pay range may vary from the range posted. ### JOB FAMILY Regulatory Operations DIVISION: ADC Diabetes Care LOCATION: France > Rungis: Miami Building ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Yes, 5 % of the Time MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Not Applicable ## At a glance - Posted by the employer: Oct 14, 2026 - First seen by OpenNash: Oct 20, 2026 - Last checked: Oct 20, 2026 - Listed for: 6 days - Employment type: Full-time[Apply on Abbott Laboratories’s careers site →](https://abbott.wd5.myworkdayjobs.com/abbottcareers/job/France--Rungis--Miami-Building/Sr-Regulatory-Affairs-Specialist--Diabete-Rungis-H-F_31164356) ## More jobs at Abbott Laboratories ### [Alternance 24 mois- Chargé(e) de Formation RH - Rungis H/F](https://jobs.opennash.com/companies/abbott-laboratories/jobs/a55ac6c2c13d3beadaa5/) ### [Business Solution Specialist- ADC- Rungis H/F](https://jobs.opennash.com/companies/abbott-laboratories/jobs/0dedbdda8ca107b99aef/) ### [Clinical Specialist Coronary (H/F) Abbott Vascular | Secteur Sud-Ouest France](https://jobs.opennash.com/companies/abbott-laboratories/jobs/22bc49cd916d21b45b67/) ### [Directeur Regional DES Ventes - Diabetologie - Marseille/Nice/ Montpellier H/F](https://jobs.opennash.com/companies/abbott-laboratories/jobs/1fd0eeebfa3666d58f4a/) ### [MSL- Division Diabète-France H/F](https://jobs.opennash.com/companies/abbott-laboratories/jobs/ab0735ae6c62859f05df/) ## Similar jobs at other companies ### [Senior Regulatory Specialist I - Toxicology, Global Regulatory Affairs](https://jobs.opennash.com/companies/ecolab/jobs/a7f265c77c592a38c347/) Ecolab · Pune, Mahārāshtra, India ### [Regulatory Affairs Specialist](https://jobs.opennash.com/companies/ecolab/jobs/2f207cd244cb549328ab/) Ecolab · Kraków, Poland ### [Principal Regulatory Affairs Professional](https://jobs.opennash.com/companies/thermo-fisher-scientific/jobs/3a8ef8a0559f4968a312/) Thermo Fisher Scientific · Remote, Mexico ### [Regulatory Affairs Specialist](https://jobs.opennash.com/companies/thermo-fisher-scientific/jobs/c80907ca1d5f566fcec5/) Thermo Fisher Scientific · Bangalore, Karnātaka, India ### [Utility Regulatory Affairs Senior Advisor](https://jobs.opennash.com/companies/edison-international/jobs/e65e0246ae95ee67c55a/) Edison International OpenNash lists jobs from employers’ own careers sites and does not handle applications. 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