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3 дня назад

Regulatory Affairs Intern (Medical Devices)

Формат работы
onsite
Тип работы
fulltime
Грейд
trainee
Английский
c1
Страна
France
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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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

hirify.global 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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