Senior Specialist QA Operations jobs in United States
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Bristol Myers Squibb · 1 day ago

Senior Specialist QA Operations

Bristol Myers Squibb is a leading biotechnology company focused on improving cancer survival through innovative drugs. The Senior Specialist, QA Operations will provide quality oversight in a Radiopharmaceutical facility, ensuring compliance and supporting clinical development and GMP commercial operations.

BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
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H1B Sponsor Likelynote

Responsibilities

Build and maintain cross functional relationships to improve processes and resolve issues
Provide quality oversight on manufacturing and validation activities
Perform real time review of manufacturing records
Perform periodic walkthroughs of manufacturing and Quality Control areas to ensure continued compliance with procedures
Provide guidance on the handling of quality and shop floor activities
Support Quality disposition process by ensuring that all required documents are accurately and properly completed and compiled against approved procedures and specifications, including all related deviations
Assist with and provide QA approval of investigations, CAPAs, change controls, validation documentation, and other related GMP documentation
Identify and report discrepancies from required work practices or procedures to management
Make sound decisions by exercising judgment within generally defined practices and policies and applies appropriate notification to management as appropriate
Participate as requested in the response team for audits and inspections by health authorities

Qualification

GMPQuality assuranceMaterial dispositionRegulatory complianceTechnical writingPrioritization skillsProblem solvingTeam playerCommunication skillsDecision making

Required

BS/MS degree in science related field (including biology, biochemistry, chemistry, engineering, or related areas)
Minimum of 5 years' experience in quality assurance and/or compliance roles in the pharmaceutical industry or a related industry
Expertise in GMP, Quality, material and product disposition
Strong capability in authoring and critically reviewing investigations, interpreting results, and generating technical conclusions consistent with Quality risk management principles
Detail-oriented with demonstrated applications in problem solving and decision-making abilities with moderate oversight from management
Team player who can work independently to achieve objectives in a fast-paced environment
Excellent verbal and written communication skills
Knowledge of US, EU and rest-of-world cGMP regulations and guidance
Well-practiced in exercising sound judgment in decision-making
Demonstrated prioritization and organization skills

Preferred

Experience working in a GMP aseptic manufacturing environment
Experience working with FDA or other regulatory authorities
Strong background and demonstrated effectiveness in quality assurance operation and compliance of clinical/commercial manufacturing

Benefits

Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Paid Time Off

Company

Bristol Myers Squibb

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At Bristol Myers Squibb, we work every day to transform patients’ lives through science.

H1B Sponsorship

Bristol Myers Squibb has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (247)
2024 (278)
2023 (231)
2022 (180)
2021 (181)
2020 (169)

Funding

Current Stage
Public Company
Total Funding
$29.32B
Key Investors
Venrock
2025-11-05Post Ipo Debt· $5.74B
2024-02-14Post Ipo Debt· $13B
2023-10-30Post Ipo Debt· $4.5B

Leadership Team

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Charles Bancroft
CFO
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Cristian Massacesi
Executive Vice President, Chief Medical Officer and Head of Development
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Company data provided by crunchbase