Compliance Specialist
1 month ago
Working with Us
At Bristol Myers Squibb, we're committed to transforming patients' lives through science. Our Regulatory Affairs team plays a vital role in ensuring the quality and integrity of our regulatory submissions. As a Regulatory Affairs Supervisor, you'll work closely with cross-functional teams to develop and implement regulatory strategies that meet the needs of our business and stakeholders.
Key responsibilities include:
- Developing and implementing regulatory strategies to support product launches and lifecycle management.
- Collaborating with global counterparts to ensure compliance with internal standards and external regulatory agency requirements.
- Maintaining statutory records, registers, and databases to ensure accurate and timely regulatory submissions.
What We Offer
Bristol Myers Squibb is a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that help patients overcome life-threatening diseases. Our company culture is built on a foundation of passion, innovation, urgency, accountability, inclusion, and integrity. We're committed to fostering a diverse and inclusive work environment that empowers our employees to grow and thrive.
On-site Protocol
Bristol Myers Squibb has a diverse occupancy structure that determines where an employee is required to conduct their work. As a Regulatory Affairs Supervisor, you may be required to work on-site at one of our facilities or participate in hybrid work arrangements. We're committed to ensuring that our employees have the necessary tools and support to succeed in their roles.
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