Specialist, Quality Assurance Shop Floor

Bristol Myers Squibb UK

Devens, MA, United States
Base: $40.16 - $48.67 ph; bonus/equity: not specif...
On-site
Quality on-the-floor oversight
Interpret problems and communicate effectively
Identify departures from approved procedures
Bristol Myers Squibb is seeking a Specialist for Quality Assurance on the shop floor in Devens, MA, to oversee compliance with quality standards and support manufacturing operations. The role involves on-site collaboration with various teams during night shifts, ensuring adherence to procedures while fostering a quality-focused culture

Job Summary

  • The Quality Assurance Shop Floor team is responsible for 24x7 Quality collaboration and oversight of site operations.
  • This position will oversee and partner with operational areas to ensure compliance with Bristol-Myers Squibb policies, standards, procedures, and Global cGMP.
  • NIGHT shift available, Panama schedule (12-hour shift patterns with a 2-2-3 work cycle including weekends and holidays).

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Specialist for Quality Assurance on the shop floor in Devens, MA, to oversee compliance with quality standards and support manufacturing operations. The role involves on-site collaboration with various teams during night shifts, ensuring adherence to procedures while fostering a quality-focused culture.

Salary

Base: $40.16 - $48.67 per hour; Bonus/Equity: Not specified; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • Quality on-the-floor oversight
  • Interpret problems and communicate effectively
  • Identify departures from approved procedures
  • Perform and document operational verification
  • Observe manufacturing operations and aseptic techniques
  • Review manufacturing batch records
  • Approve deviation records independently
  • Experience with GxP electronic systems

Nice-to-have

  • Action-oriented and proficient decision-making
  • Build and maintain relationships
  • Seek collaborative solutions
  • Champion for quality-culture
  • Ability to work in cleanroom environments

Key Requirements

  • Bachelor's degree in STEM field or equivalent experience
  • 2+ years of relevant cGMP experience
  • 1+ year of manufacturing site experience
  • Experience in FDA/EMA regulations

Work Rights

Not specified

Tailored Resume

Cover Letter