Job description We are looking for a Regulatory Affairs Specialist to join Amaris and work for one of our clients, a leader in its sector.

Your responsibilities: Responsible for the legal aspects of the study, as well as the drafting, submission, and validation of regulatory documents.

The main point of contact for regulatory authorities, ensuring that products are manufactured and distributed in compliance with the appropriate legislation.

Drafting of documents, submissions, renewals in accordance with the requirements of regulatory affairs authorities to obtain the right to issue the CS (Certificate of Safety) or to update it.

Your qualifications: Degree: Master's or Pharmacist (or Doctor).

Schools: University or pharmacy studies.

Specialties: Possibility of specialization based on the product (medicine, medical devices, cosmetics...), local level (subsidiaries)/global level (headquarters), countries/regions (EMEA/Asia...).

Our corporate culture: Agility: Evolve in a flexible, dynamic, and stimulating environment.

International: Benefit from international collaborations and numerous mobility opportunities.

Intrapreneurship: Get involved in parallel initiatives or develop your own Business Unit.

Listening Management: Benefit from personalized support throughout your professional journey.

Amaris Consulting is committed to diversity and inclusion.

We welcome applications from all qualified individuals, regardless of gender, sexual orientation, race, ethnic origin, beliefs, age, marital status, disability, or any other characteristic.