Regulatory Affairs Specialist

il y a 2 semaines


RueilMalmaison, Île-de-France Bristol Myers Squibb Temps plein

Transforming Patients' Lives through Science

Bristol Myers Squibb is a leading pharmaceutical company dedicated to transforming patients' lives through science. We are seeking a highly skilled Regulatory Affairs Specialist to join our team in France.

About the Role

As a Regulatory Affairs Specialist, you will be responsible for ensuring compliance with regulatory requirements and guidelines in France. You will work closely with our cross-functional teams to develop and implement regulatory strategies that support the launch of new products.

Key Responsibilities

  • Verify and approve promotional materials and training documents in compliance with regulatory requirements.
  • Prepare and update risk minimization tools for products under your responsibility.
  • Collaborate with internal Pharmacovigilance teams to ensure compliance with regulatory requirements.
  • Contribute to the development of regulatory strategies and plans for new products.
  • Support the Director of Regulatory Affairs in ensuring compliance with regulatory requirements.

Requirements

  • Pharmacist with specialization in Regulatory Affairs.
  • At least 1 year of experience in Regulatory Affairs, preferably in the pharmaceutical industry.
  • Excellent communication and teamwork skills.
  • Ability to work in a fast-paced environment and adapt to changing priorities.
  • Proficiency in Microsoft Office.

What We Offer

Bristol Myers Squibb offers a unique and challenging work environment that allows you to grow and develop your skills. We are committed to diversity and inclusion and offer a range of benefits to support your well-being and career development.


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