Quality Assurance Senior Specialist, Site Support

Bristol Myers Squibb

Devens, MA, US
Base: $89,530 - $108,490; bonus/equity: + incentiv...
50% onsite
Quality review and approval of deviations
Quality review and approval of change controls
Support for technology transfer
Support Devens site through review and approval of investigations and change controls, providing Quality oversight and support for Technology Transfer, Automation, Cell Bank Disposition, Validation, Manufacturing Science and Technology, Master Data and Site Engineering programs

Job Summary

  • Support Devens site through review and approval of investigations and change controls, providing Quality oversight and support for Technology Transfer, Automation, Cell Bank Disposition, Validation, Manufacturing Science and Technology, Master Data and Site Engineering programs.
  • Assure the quality of manufactured products are in compliance with all applicable regulations and guidelines, and may assist in preparing for and hosting of regulatory and customer audits.
  • Bristol Myers Squibb offers a wide variety of competitive benefits, services and programs that provide employees with resources to pursue their goals, both at work and in their personal lives.

Matching Summary

Support Devens site through review and approval of investigations and change controls, providing Quality oversight and support for Technology Transfer, Automation, Cell Bank Disposition, Validation, Manufacturing Science and Technology, Master Data and Site Engineering programs.

Salary

Base: $89,530 - $108,490; Bonus/Equity: Additional incentive cash and stock opportunities; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • Quality review and approval of deviations
  • Quality review and approval of change controls
  • Support for Technology Transfer
  • Review and approval of automation change management
  • Review and approval of Master Data for SAP and Syncade
  • Review and approval of Maximo work orders

Nice-to-have

  • Team-based environment experience
  • Diverse group of people experience
  • Participate in cross functional meetings
  • Apply appropriate notification to management

Key Requirements

  • B.S. in science, engineering, biochemistry or related discipline, or equivalent
  • Minimum of 4 years of relevant experience
  • At least 2 years focused on product quality
  • Knowledge of US and EU cGMP regulations and guidance
  • Experience working in a team-based environment

Work Rights

Not specified

Tailored Resume

Cover Letter