QA Jobs at Bristol- Apply Now & Explore QA Careers Today
Bristol Myers Squibb (BMS) is seeking a QA Shop Floor Specialist to join its cutting-edge cell therapy manufacturing facility in Bothell, Washington. This role offers an opportunity to make a direct impact on patient lives through real-time quality oversight in a cGMP-regulated environment. Ideal for professionals passionate about quality assurance, regulatory compliance, and cell therapy manufacturing, this position places you at the heart of life-changing science with a company recognized for its innovation, inclusivity, and purpose-driven culture.
Job Details:
- Position: Specialist – QA Shop Floor
- Location: Bothell – WA – US
About the Company:
At Bristol Myers Squibb (BMS), every employee contributes to a single inspiring vision — Transforming patients’ lives through science™. BMS is a global biopharmaceutical leader focused on discovering, developing, and delivering innovative medicines for serious diseases. With a culture that values innovation, inclusion, accountability, and integrity, BMS offers challenging yet rewarding careers that make a difference. The company’s mission-driven environment empowers employees to grow professionally while improving patient outcomes worldwide.
QA Jobs at Bristol- Role:
The QA Specialist– Shop Floor provides real-time quality assurance oversight for clinical and commercial cell therapy operations. This role ensures compliance with Good Manufacturing Practices (cGMP), Good Documentation Practices (GDocP), and ALCOA+ principles, supporting manufacturing excellence and data integrity across production lines.
QA Jobs at Bristol- Key Responsibilities:
- Perform real-time batch record review and collaborate with manufacturing teams to resolve discrepancies.
- Conduct QA walkthroughs, Gemba, and process observations to ensure adherence to cGMP and aseptic techniques.
- Review and approve operational documents such as Standard Operating Procedures (SOPs) and Work Instructions.
- Lead deviation triage activities, applying quality risk management principles to ensure timely investigation and closure.
- Participate in continuous improvement initiatives such as Kaizen, 5S, and cross-functional gemba events.
- Serve as a subject matter expert (SME) for cGMP and quality practices on the shop floor.
Qualifications:
Education:
- Bachelor’s degree in a STEM field (Science, Technology, Engineering, Mathematics) preferred.
- Associate degree with equivalent experience will be considered.
Experience:
- 3–4 years of cGMP experience in a regulated environment (pharmaceuticals, biotechnology, or cell therapy).
- Proficiency in systems such as MES, ERP (SAP), Infinity, and BMSDocs.
- Strong understanding of batch record review, deviation management, and product disposition.
- Excellent organizational, analytical, and decision-making skills.
- Detail-oriented with a focus on quality risk management and right-first-time execution.
Schedule:
- Full-time; choice between:
- Sun–Wed | 10:30 AM – 9:00 PM
- Wed–Sat | 10:30 AM – 9:00 PM
Compensation & Benefits Offered for QA Careers:
- Pay Range: $38.42 – $46.55 per hour (based on experience and location)
- Comprehensive Benefits Package including:
- Medical, dental, and vision coverage
- 401(k) with company match
- Paid vacation, holidays, and volunteer days
- Well-being support programs and EAP services
- Tuition reimbursement and recognition programs
Why Join BMS:
At Bristol Myers Squibb, you’ll work on uniquely interesting and life-changing projects within a collaborative, innovative, and flexible environment. Whether you’re ensuring quality on the shop floor or supporting a major breakthrough in cell therapy, every contribution you make helps transform patient outcomes and advances global health.
