Regulatory Affairs Specialist
4 weeks ago
Transforming Patients' Lives through Science
Bristol Myers Squibb is a leading biopharmaceutical company that is transforming patients' lives through science. We are seeking a highly skilled Regulatory Affairs Specialist to join our team.
The successful candidate will be responsible for independently handling regulatory submissions to health authorities, collaborating with global counterparts and other functions to devise regulatory strategy, and ensuring compliance with internal standards and external regulatory agency requirements.
The ideal candidate will have a strong understanding of regulatory requirements and a proven track record of delivering high-quality regulatory submissions. They will also be able to work effectively in a team environment and communicate complex information to stakeholders.
Key Responsibilities:
- Independently handle regulatory submissions to health authorities
- Collaborate with global counterparts and other functions to devise regulatory strategy
- Ensure compliance with internal standards and external regulatory agency requirements
- Monitor regulatory and industry changes and seek opportunities to improve efficiency of regulatory submission
- Provide regulatory advice and support to other functions to meet regulatory and business requirements
What We Offer:
- A dynamic and inclusive work environment
- Opportunities for professional growth and development
- A competitive salary and benefits package
How to Apply:
If you are a motivated and detail-oriented individual with a passion for regulatory affairs, please submit your application, including your resume and a cover letter, to [insert contact information].
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