QC Specialist

Bristol Myers SquibbBothell, WA
$38 - $46Onsite

About The Position

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Requirements

  • Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
  • Apply scientific principles to analytical testing and the proper use of laboratory equipment.
  • Ability to communicate effectively with peers and management regarding task completion, roadblocks, and needs.
  • Attention to detail and demonstrated organizational skills.
  • Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
  • Bachelor's degree preferred in science. Associate degree with equivalent combination of education and work experience may be considered.
  • 0-2+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.
  • Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.
  • Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.

Nice To Haves

  • Prior experience in analytical testing (e.g., pH, Osmolality, FTIR, HPLC, etc.) is preferred.
  • Prior experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, aseptic technique) is preferred.

Responsibilities

  • Perform routine testing of raw materials and perform sampling of retains.
  • Ship samples to outside testing labs, as needed.
  • May review GMP documentation and perform data verification.
  • Support document revision, project, CAPA and deviation/ investigation related tasks and/or continuous improvement efforts.
  • May train others on general job duties.
  • Perform other tasks as assigned.

Benefits

  • wellbeing support
  • retirement and financial protection benefits
  • insurance offerings (medical, dental, vision, life and disability)
  • Flexible Time Off (FTO)
  • 11 paid company holidays each year
  • 160 hours of paid vacation annually for new hires
  • 3 optional holidays
  • paid sick leave
  • up to two paid volunteer days per year
  • summer hours flexibility
  • leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs
  • annual Global Shutdown between Christmas Day and New Year's Day
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