Senior Quality Auditor jobs in United States
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Bristol Myers Squibb · 12 hours ago

Senior Quality Auditor

Bristol Myers Squibb is a dynamic biotechnology company focused on improving survival rates for cancer patients through innovative drug development. The Senior Quality Auditor will be responsible for planning, executing, and reporting on audits to ensure compliance with GxP regulations and support the continuous improvement of the Quality Management System.

BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
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H1B Sponsor Likelynote

Responsibilities

Plan, schedule, and conduct audits of internal departments, suppliers, and service providers in accordance with the audit program
Evaluate compliance with applicable regulatory requirements (e.g., FDA, EMA, ICH), internal SOPs, and quality agreements
Document audit findings and collaborate with stakeholders to develop effective CAPAs
Track and verify the implementation and effectiveness of CAPAs
Maintain audit records and ensure timely communication of audit outcomes
Support regulatory inspections and inspection readiness activities
Provide guidance and training on audit processes and GxP compliance expectations
Participate in continuous improvement initiatives related to quality systems and audit processes
Travel to supplier sites and other company locations may be required

Qualification

GxP regulationsAuditing experienceAuditor certificationElectronic quality systemsInternational auditsAnalytical skillsReport-writing skillsCommunication skillsIndependent work

Required

Bachelor's degree in Life Sciences, Chemistry, or related field is required
Minimum of 7-10 years of experience in quality assurance, auditing, or supplier management within the pharmaceutical, biotechnology, or cGMP industry
Auditing experience within regulated biotech/pharma industry or equivalent in a GxP-regulated environment, with at least 3 years in auditing or quality assurance
Experience conducting audits across GMP, GLP, and/or GCP domains
Experience with international audits and regulatory inspections is required
Strong knowledge of global GxP regulations and standards (e.g., 21 CFR Parts 11, 210, 211; EudraLex Volume 4; ICH Guidelines) is required
Excellent analytical, communication, and report-writing skills are required
Must be capable of working independently and handling several tasks simultaneously

Preferred

Auditor certification (e.g., ASQ CQA, RQAP-GCP) is strongly preferred
Familiarity with electronic quality systems and audit management tools is preferred

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