Bristol Myers Squibb
Senior Supplier Quality Auditor
Remote - United States - US · Senior · Part-time
Sponsorship not specified$10k-$15kDetected 4 hours ago
GCPAccessibilityStakeholder ManagementExcelAuditingGMPFDA RegulatoryCommunicationCollaborationWritingGxP
> stay_score
odds of building a lasting career here
38Risky
Cap-exempt (no lottery)0
Sponsors this role85
Entry-level history0
PERM / green-card track0
Lottery odds (Level I)39
Fits your clock70
Thin sponsorship signal and lottery-bound (~15% per draw). A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.
Lottery odds assume a STEM candidate.
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About the role
- Additional incentive cash and stock opportunities (based on eligibility) may be available.
- Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment.
- Medical, pharmacy, dental, and vision care.
Responsibilities
- Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager.
Requirements
- Domestic travel to supplier sites is required.
- Bachelor's degree in Life Sciences, Chemistry, or a related field or equivalent experience.
- Minimum of 7 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.
- Strong knowledge of global GxP regulations and standards (e.g., 21 CFR Parts 11, 210, 211
- Experience conducting audits across GMP, GLP, and/or GCP domains.
Skills
- Proven ability to identify systemic quality and compliance risks
- Excellent analytical, communication, and report-writing skills.
- Ability to work independently and manage multiple priorities.
- Ability to utilize AI tools to enhance individual productivity and quality of work
- Strong technical writing skills for audit reports and regulatory documentation
- Sound quality judgment and ability to work independently
- Strong communication and stakeholder management skills
- Uses AI tools to enhance individual productivity and quality of work
Compensation
- Compensation Overview:
Company info
- Here, you'll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do.
- If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com.
- Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer.
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This listing is sourced directly from Bristol Myers Squibb's careers page and normalized into a canonical job model.