Specialist, Aseptic Observation Program

Bristol Myers Squibb

Summit West, NJ, US
Base: $34.92 - $42.32 ph; bonus/equity: + incentiv...
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Proven proficiency in coaching front-line operators
Extensive knowledge of sops and cgmps
Understanding of aseptic processing principles
** Bristol Myers Squibb is seeking a Specialist for their Aseptic Observation Program in Summit West, NJ. The role involves observing aseptic techniques on the manufacturing floor, providing coaching, and ensuring adherence to contamination control strategies, with a focus on collaboration across teams. **

Job Summary

  • This role involves performing aseptic observations on the manufacturing floor to assess operator behaviors and adherence to contamination control strategies.
  • The position requires documenting observations accurately and providing actionable coaching and feedback for observed personnel and area management.
  • Bristol Myers Squibb offers a wide variety of competitive benefits including health coverage, financial well-being programs, and flexible paid time off.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Specialist for their Aseptic Observation Program in Summit West, NJ. The role involves observing aseptic techniques on the manufacturing floor, providing coaching, and ensuring adherence to contamination control strategies, with a focus on collaboration across teams. **

Salary

Base: $34.92 - $42.32 per hour; Bonus/Equity: Additional incentive cash and stock opportunities available based on eligibility; Benefits: Comprehensive health, dental, vision, 401(k), and paid time off included

Skills & Requirements

Must-have

  • Proven proficiency in coaching front-line operators
  • Extensive knowledge of SOPs and cGMPs
  • Understanding of aseptic processing principles
  • Strong observational and analytical abilities
  • Experience in cell therapy or bioprocessing manufacturing

Nice-to-have

  • Experience with ISO 5/Grade A biosafety cabinets
  • Ability to adapt to fast-paced complex environment
  • Partnership skills with Sterility Assurance teams
  • Root cause analysis and CAPA development experience

Key Requirements

  • Bachelor's degree in relevant science or engineering discipline
  • 3+ years of experience in cGMP cell therapy or bioprocessing manufacturing
  • Work authorization status not specified in posting

Work Rights

Not specified

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