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Director, Clinical Supply Quality
Company Name
Bristol Myers Squibb
Job Overview
The Director, Clinical Supply Quality is responsible for global regulatory compliance of clinical supplies and oversight of related activities, including:
- Internal packaging
- Global labeling operations
- ISR studies
- PAA/PSDA studies
- IMP supply/management
This role provides leadership in resolving critical quality issues and acts as a Quality Culture ambassador, influencing senior leadership on continuous quality improvements.
Requirements
- BS degree
- 13-15 years of experience (5+ in a regulated function)
- Strong knowledge of CTA requirements
- Quality Management experience
- Expertise in cGMP/EU GMP regulations