QA Operations Specialist Job – at Bristol Myers, Apply Now!
Looking to grow your career in Quality Assurance within a global biopharmaceutical powerhouse? Bristol Myers Squibb is hiring a Specialist in Quality Assurance Operations at our cutting-edge Devens, MA site. Join a company that transforms lives through science, with opportunities to work on advanced biologics manufacturing and ensure products meet the highest standards of GMP compliance and patient safety. If you’re a detail-oriented professional with QA or GMP experience in biotech or pharma, this is your chance to contribute to meaningful, life-changing work.
- Job Position: Specialist, Quality Assurance Operations
- Location: Devens, MA, USA
- Shift: MondayโFriday | 10:30 AM to 7:00 PM
- Department: Quality Assurance โ Operations
- Employment Type: Full-Time | Onsite
- Compensation Range: $81,800 โ $99,100 + Incentives
About The Company
Bristol Myers Squibbโs Devens campus is a state-of-the-art manufacturing facility supporting the production of biologics and cell therapies that impact lives globally. With a collaborative culture and a mission-driven workforce, BMS offers a dynamic environment where innovation meets purpose.
QA Operations Specialist Job – About the Role
As a QA Operations Specialist, youโll provide on-the-floor quality oversight and support routine manufacturing of biologics, ensuring all activities align with cGMP regulations, internal SOPs, and corporate quality standards. Youโll also be involved in batch record reviews, documentation audits, deviation support, and inspection readiness, playing a vital role in delivering therapies to patients faster and safer.
QA Operations Specialist Job – Key Responsibilities
- Provide QA floor support for GMP manufacturing operations.
- Review batch production records for media, buffer, and cryo operations.
- Conduct walkthroughs in GMP areas, identifying and documenting concerns.
- Support return-to-service and inspection readiness walkthroughs.
- Review paper and electronic documentation for GMP compliance.
- May assist in deviation investigations and product release.
- Review alarms, logbooks, and quality-related documentation.
- Support cross-functional quality initiatives as needed.
QA Operations Specialist Job – Qualifications & Experience
- A B.S. in science, engineering, or biochemistry or a related field is preferred.
- 2+ years of experience in a regulated biotech or pharmaceutical environment (Co-Op experience considered).
- Familiarity with US/EU cGMP guidelines and industry standards.
- Strong command of MS Word, Excel, and quality documentation tools.
- Experience with electronic batch records, DeltaV, and quality systems is desirable.
- Excellent attention to detail, communication skills, and teamwork.
Why Join Us
- Competitive compensation with incentive cash and stock options.
- Comprehensive benefits include medical, dental, vision, 401(k), wellness, and insurance plans.
- Paid time off, global shutdown days, and flexible work-life policies.
- Professional growth through learning & development programs and internal mobility.
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