3 дня назад
Regulatory Affairs Intern (Medical Devices)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Regulatory Affairs Intern (Medical Devices) (Medical Devices/Pharmaceuticals): Supporting regulatory compliance for medical devices and combination products throughout their lifecycle with an accent on regulatory documentation, gap assessments, standards monitoring, and cross-functional coordination. Focus on evaluating regulatory changes, maintaining compliance records, preparing audit materials, and tracking regulatory deliverables.
Location: Lyon, France; onsite internship for 6 months starting March 2027.
Company
manufactures drug delivery systems and provides development, industrialization, manufacturing, and contract manufacturing services for the pharmaceutical industry.
What you will do
- Support the preparation, maintenance, organization, and updating of regulatory documentation throughout the product lifecycle.
- Perform document gap assessments and collect, consolidate, verify, and maintain regulatory data.
- Monitor regulatory and standards updates and assess their impact on products and technical changes.
- Prepare regulatory summaries, reports, presentations, meeting minutes, and status updates.
- Assist Regulatory Affairs Project Managers with regulatory activities, project tracking, deliverables, customer requests, and authority requests.
- Support audits, corrective-action follow-up, compliance initiatives, regulatory databases, and document management systems.
Requirements
- Master's degree student at Bac+4/Bac+5 level in Regulatory Affairs, Biomedical Engineering, or Pharmaceutical Sciences, or experience in medical devices, pharmaceuticals, or combination devices.
- Fluent English and French required.
- Strong attention to detail, rigor, analytical ability, and organizational skills.
- Autonomous, proactive, solution-oriented approach with curiosity and willingness to learn.
- Ability to work in a multicultural and cross-functional environment.
Culture & Benefits
- Exposure to global medical device regulations and strategic regulatory projects.
- Collaboration with Regulatory Affairs, Quality, Design, Project Management, Manufacturing, and other cross-functional teams.
- International working environment within a global medical device manufacturer.
- Transparent recruitment process with application review, screening interview, hiring manager interview, and offer stages.
Hiring process
- Application review by the Talent Acquisition team.
- Initial screening interview followed by a Hiring Manager interview.
- Offer after successful completion of the process.
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