Staff Specialist, Regulatory Affairs (H/F)

Stryker · Lyon, France

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RegulatoryFull-timeCompany career page

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What they're looking for

Master's degree in engineering, sciences, or regulatory sciences
Minimum 4 years of professional experience in regulatory affairs
Professional-level English proficiency
RAC certification or Master's qualification preferred
Orthopedic industry experience is advantageous
Strong teamwork and communication abilities
Ability to adapt quickly and manage unforeseen situations

What you'll be doing

Develop and implement local, national, and international regulatory strategies for medical devices
Prepare, execute, and support regulatory registration dossiers for export markets
Manage regulatory activities related to product development and modifications including CE marking
Communicate with notified bodies, competent authorities, and external auditors
Monitor regulatory and normative developments and assess impact on quality management systems

Compensation€47,800–€79,700 EUR annual

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