Regulatory Affairs Specialist
2 months ago
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 strategy, driving efficiency and innovation in regulatory submissions.
- Monitor regulatory and industry changes, identifying opportunities to improve the efficiency of regulatory submissions and ensuring compliance with evolving requirements.
- Provide regulatory advice and support to other functions, ensuring that business requirements are met while maintaining regulatory compliance.
- Maintain statutory records, registers, and databases, ensuring accurate and timely filing.
At Bristol Myers Squibb, we offer a unique and inclusive work environment that promotes diversity, innovation, and collaboration. Our employees are empowered to apply their individual talents and perspectives to drive meaningful work that transforms patients' lives. 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, and 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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