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Approach People Recruitment recrutement

Head Of Regulatory Affairs H/F Approach People Recruitment

Genève-Annemasse - 74
CDI
Offre d’un cabinet de recrutement -
Résumé de l'offre
  • 80 000 - 150 000 € / an
  • Bac +5
  • Services aux Entreprises
  • Exp. + 7 ans

Détail du poste

As the Head of Regulatory Affairs, you will BE responsible for overseeing and leading the regulatory affairs team for a company specializing in medical devices. You will work closely with the research and development, quality, manufacturing, marketing, and sales departments to ensure regulatory compliance for all products and processes.

Responsibilities :
- Manage and lead the regulatory affairs team, including activity planning, goal setting, and performance evaluation.
- Develop and implement regulatory strategies to ensure compliance with local and international standards.
- Ensure timely and effective submission of regulatory filings to relevant authorities, including new product approvals, renewals, and modifications.
- Evaluate regulatory requirements for new products and changes to existing products, providing strategic guidance to the product development team.
- Manage interactions with regulatory agencies and external partners, ensuring effective and positive relationships.
- Maintain constant regulatory surveillance to identify new requirements and potential regulatory developments impacting the company.
- Collaborate with internal teams to develop and implement regulatory compliance management processes and systems.
- Participate in internal and external audits related to regulatory affairs, ensuring appropriate corrective and preventive actions are implemented.
- Provide regulatory expertise and guidance to other departments within the company, including training on applicable regulatory requirements.

Your profil :
- University degree in life sciences, biomedical engineering, or a related field.
- At least 10 years experience in regulatory affairs, preferably in the medical devices sector.
- In-depth knowledge of local and international regulations related to medical devices, such as FDA, EMA, and European directives.
- Proven experience in team management and leadership.
- Excellent communication skills and demonstrated ability to work collaboratively with multifunctional teams.
- Ability to work independently, manage priorities, and meet tight deadlines.
- Proficiency in English and German, both spoken and written; proficiency in french would BE an advantage.

Head Of Regulatory Affairs H/F
  • Genève-Annemasse - 74
  • CDI
Publiée le 21/03/2025 - Réf : 20786

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