Specialist, Quality Assurance Validation jobs in United States
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Bristol Myers Squibb · 12 hours ago

Specialist, Quality Assurance Validation

Bristol Myers Squibb is a company dedicated to transforming patients' lives through science. They are seeking a Specialist in Quality Assurance Validation to perform independent reviews and approvals of quality lifecycle documents and provide guidance on quality issues during regulatory inspections.

BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
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H1B Sponsor Likelynote

Responsibilities

Perform independent review and approval of initial Commissioning, Qualification, and Validation (CQV) lifecycle documents and subsequent changes
Review and approval of periodic reviews, re-qualification, decommissioning and retirement and plans, protocols, and summary reports
Review and approval of Standard Operating Procedures, Work Instructions, Deviations, CAPAs and Change Controls related to facilities, utilities, equipment, instruments, and systems
Provide instruction and guidance on CQV quality issues during regulatory agency inspections, deviations, and CAPA discussions
Support the Contract Service Providers program
Provide reports to management related to timely deviation completions, CAPA implementations or other issues related to CQV and CSV activities
Support Product Development and Product Development Quality initiatives as needed
Bring to the attention of management, any information relating to the impact of policies, procedures, and industry quality regulations on quality systems

Qualification

CQV experienceCGMP regulationsPharmaceutical manufacturingProcess control systemsLaboratory equipmentMS Office SuiteInterpersonal skillsOrganizational skillsLeadership skills

Required

Master of Science or a Bachelor of Science with 3-5 years' experience, including 1-3 years' experience in regulated function
Experience as a CQV, QA, and/or QC representative within Pharmaceutical/Drug Substance Manufacturing (API, Sterile, Non-Sterile or Biological products) or Medical Device Manufacturing or Laboratory environment
Demonstrated knowledge and experience in cGMP regulations
Working knowledge in the following: Process control systems, Process equipment & utilities, Laboratory equipment & instrumentation, Packaging & Labelling equipment, Environmental monitoring systems, Supply Chain systems
Effective interpersonal and organizational skills
Demonstrated leadership skills
Proficiency with MS Office Suite

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