Regulatory Affairs Specialist

3 weeks ago


Hong Kong, Central and Western District, Hong Kong SAR China Bristol Myers Squibb Full time
Transforming Patients' Lives through Science

Bristol Myers Squibb is a leading biopharmaceutical company that is dedicated to transforming patients' lives through science. We are seeking a highly skilled Regulatory Affairs Supervisor to join our team.

Key Responsibilities:
  • Independently handle regulatory submissions to health authorities, ensuring compliance with internal standards and external regulatory agency requirements.
  • Collaborate with global counterparts and other functions to devise regulatory strategies that meet business needs.
  • Monitor regulatory and industry changes to identify opportunities for improving efficiency in regulatory submissions.
  • Provide regulatory advice and support to other functions to ensure compliance with regulatory requirements.
  • Maintain statutory records, registers, and databases, and ensure routine filing is completed accurately and on time.
What We Offer:

At Bristol Myers Squibb, we offer a unique and inclusive work environment that promotes diversity in clinical trials. Our shared values of passion, innovation, urgency, accountability, inclusion, and integrity bring out the highest potential of each of our colleagues. We are committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations, and ongoing support in their roles.

We care about the well-being of our staff, customers, patients, and communities. As a result, we strongly recommend that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

We are an equal opportunities employer and welcome applications from qualified candidates with arrest and conviction records, pursuant to applicable laws in your area.



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