Regulatory Affairs Specialist
il y a 2 semaines
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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