Compliance Specialist

1 month ago


Hong Kong, Central and Western District, Hong Kong SAR China Bristol Myers Squibb Full time

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:

  1. Developing and implementing regulatory strategies to support product launches and lifecycle management.
  2. Collaborating with global counterparts to ensure compliance with internal standards and external regulatory agency requirements.
  3. 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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