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Regulatory affair Specialist

Approach People Recruitment

Paris, Île-de-France, France Full-time June 25, 2026
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Opportunity Description

As a Regulatory Affairs Specialist, you will be responsible for ensuring compliance with regulatory requirements related to the development, approval, and marketing of pharmaceutical, medical device, or other healthcare products. You will work closely with cross-functional teams to navigate the complex regulatory landscape and to ensure that products meet all applicable regulations and standards.

Responsibilities:

  • Develop and implement regulatory strategies for product development, registration, and commercialization.
  • Prepare and submit regulatory submissions, including Investigational New Drug (IND), New Drug Application (NDA), 510(k), Pre-Market Approval (PMA), or other regulatory filings, as required.
  • Liaise with regulatory agencies, such as the FDA, EMA, or other regulatory authorities, to facilitate the review and approval process for new products or product changes.
  • Provide regulatory guidance and support to cross-functional teams, inc...
    • Full-time Business Operations Specialists

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    Opportunity Details

    Location Paris, Île-de-France
    Country France
    Type Full-time
    Category Business Operations Specialists
    Posted June 25, 2026
    Deadline August 04, 2026

    About Approach People Recruitment

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    Approach People Recruitment

    Paris, France

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