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Radiopharma Validation Lead - GMP & Process Excellence

Bristol-Myers Squibb

Bristol-Myers Squibb is seeking a Lead Validation Engineer in Indianapolis to support radiopharmaceutical facility operations. This role leads validation activities and provides technical guidance on GMP compliance, ensuring quality in our mission to develop transformative therapies. The ideal candidate will have over 8 years of experience in regulated environments, strong leadership skills, and expertise in validation processes. This is an exciting opportunity to drive significant impact in the fight against cancer. #J-18808-Ljbffr

Vacancy posted 1 day ago
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