3+ years cgmp cell therapy or bioprocessing experience
Proven proficiency in coaching front-line operators
Extensive knowledge of sops and regulatory environment
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Bristol Myers Squibb is seeking a Specialist for its Aseptic Observation Program in Summit West, NJ, to ensure compliance with aseptic practices and provide coaching to manufacturing personnel. The role requires a strong understanding of cGMP and aseptic processing principles, along with the ability to document and provide actionable feedback on operator behaviors.
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Job Summary
This role involves performing aseptic observations on the manufacturing floor to assess operator behaviors and adherence to Contamination Control Strategy principles.
The position requires partnering with Sterility Assurance, Manufacturing, and Quality teams to refine observation procedures and support improvements to contamination control strategies.
Bristol Myers Squibb offers a wide variety of competitive benefits including health coverage, financial well-being programs, and flexible paid time off options.
Matching Summary
Match Score: 75
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Bristol Myers Squibb is seeking a Specialist for its Aseptic Observation Program in Summit West, NJ, to ensure compliance with aseptic practices and provide coaching to manufacturing personnel. The role requires a strong understanding of cGMP and aseptic processing principles, along with the ability to document and provide actionable feedback on operator behaviors.
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Salary
Base: $34.92 - $42.32 per hour; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health coverage, 401(k), paid time off, and wellness programs included
Skills & Requirements
Must-have
3+ years cGMP cell therapy or bioprocessing experience
Proven proficiency in coaching front-line operators
Extensive knowledge of SOPs and regulatory environment
Understanding of aseptic processing principles
Strong observational and critical-thinking abilities
Nice-to-have
Experience with ISO 5 Grade A biosafety cabinets
Background in cell therapy manufacturing observations
Ability to adapt to fast-paced complex environments
Partnership skills with Sterility Assurance teams
Key Requirements
Bachelor's degree in relevant science or engineering discipline
3+ years of experience in cGMP cell therapy or bioprocessing manufacturing
Work authorization for the United States (implied by location)