Senior Level Quality Assurance Supervisor Jobs
Senior level quality assurance supervisor jobs place experienced professionals in charge of quality systems, compliance outcomes, and the cross-functional teams that keep manufacturing and production standards on target. Roles are concentrated across Biotechnology & Pharmaceuticals, Consulting & Professional Services, and Technology & Software, with a mix of on-site, hybrid, and remote opportunities, and employers like United Pharma, Revolution Medicines, and Revolution Medicines hiring at this level now.
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INTRODUCTION
Quality Assurance Manager This position collaborates closely with Clinical Supply Chain, CMC, Regulatory Affairs, Clinical Operations, and external partners to resolve quality issues, support timely release of Investigational Medicinal Products (IMPs), and maintain inspection readiness.
QUALIFICATIONS AND EXPERIENCE
- Bachelor's degree in a scientific discipline, pharmaceutical sciences, or a related field; equivalent relevant experience may be considered.
- Typically 7+ years of experience in Pharmaceutical Quality Assurance, Quality Operations, or a related GMP-regulated function, including demonstrated experience supporting clinical packaging and labeling operations.
- Demonstrated experience reviewing and approving clinical packaging and labeling batch records and supporting documentation.
- Experience supporting clinical trial material release, IMP disposition, expiry extension assessments, temperature excursion investigations, and release restriction decisions.
- Strong working knowledge of GMP requirements applicable to Investigational Medicinal Products (IMPs), clinical packaging and labeling, and outsourced manufacturing operations.
- Experience managing or providing QA oversight of deviations, investigations, CAPAs, change controls, and documented product impact assessments.
- Experience working with external CMOs and pharmaceutical service providers.
- Experience with vendor quality oversight, audits, quality agreements, and inspection readiness preferred.
- Familiarity with electronic quality management systems and document management platforms.
- Experience supporting early-phase clinical development programs and managing competing clinical supply priorities preferred.
- Strong technical writing, documentation review, and risk assessment skills.
- Sound judgment and the ability to make timely, scientifically justified, risk-based quality decisions.
- Demonstrated leadership and influencing skills in a matrixed environment.
- Strong organizational and project management skills, with the ability to manage multiple priorities and time-sensitive clinical supply activities.
- Effective communication and collaboration skills with internal stakeholders and external partners.
The role requires effective coordination with external manufacturing, packaging, labeling, storage, and distribution partners, as well as close collaboration with Clinical Supply Chain, CMC, Regulatory Affairs, Clinical Operations, and Quality. Periodic domestic travel may be required to support vendor oversight, on-site packaging and labeling activities, audits, inspections, and other quality initiatives.
INTRODUCTION
Quality Assurance Manager This position collaborates closely with Clinical Supply Chain, CMC, Regulatory Affairs, Clinical Operations, and external partners to resolve quality issues, support timely release of Investigational Medicinal Products (IMPs), and maintain inspection readiness.
QUALIFICATIONS AND EXPERIENCE
- Bachelor's degree in a scientific discipline, pharmaceutical sciences, or a related field; equivalent relevant experience may be considered.
- Typically 7+ years of experience in Pharmaceutical Quality Assurance, Quality Operations, or a related GMP-regulated function, including demonstrated experience supporting clinical packaging and labeling operations.
- Demonstrated experience reviewing and approving clinical packaging and labeling batch records and supporting documentation.
- Experience supporting clinical trial material release, IMP disposition, expiry extension assessments, temperature excursion investigations, and release restriction decisions.
- Strong working knowledge of GMP requirements applicable to Investigational Medicinal Products (IMPs), clinical packaging and labeling, and outsourced manufacturing operations.
- Experience managing or providing QA oversight of deviations, investigations, CAPAs, change controls, and documented product impact assessments.
- Experience working with external CMOs and pharmaceutical service providers.
- Experience with vendor quality oversight, audits, quality agreements, and inspection readiness preferred.
- Familiarity with electronic quality management systems and document management platforms.
- Experience supporting early-phase clinical development programs and managing competing clinical supply priorities preferred.
- Strong technical writing, documentation review, and risk assessment skills.
- Sound judgment and the ability to make timely, scientifically justified, risk-based quality decisions.
- Demonstrated leadership and influencing skills in a matrixed environment.
- Strong organizational and project management skills, with the ability to manage multiple priorities and time-sensitive clinical supply activities.
- Effective communication and collaboration skills with internal stakeholders and external partners.
The role requires effective coordination with external manufacturing, packaging, labeling, storage, and distribution partners, as well as close collaboration with Clinical Supply Chain, CMC, Regulatory Affairs, Clinical Operations, and Quality. Periodic domestic travel may be required to support vendor oversight, on-site packaging and labeling activities, audits, inspections, and other quality initiatives.
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Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals11
- Consulting & Professional Services8
- Technology & Software5
- Retail2
- Medical Devices2
Senior Level Quality Assurance Supervisor Jobs: Frequently Asked Questions
How do I get a senior level quality assurance supervisor job?
Employers at this level want candidates who have owned quality management systems end to end, led audits independently, and driven measurable improvements in defect rates or compliance outcomes. Certifications like CQE or ASQ credentials carry real weight, as does demonstrated experience mentoring junior QA staff and presenting quality data to operations leadership. Tailoring your resume to show scope of authority, not just task completion, sets you apart.
Which companies hire senior level quality assurance supervisors?
Companies hiring senior level quality assurance supervisors right now include United Pharma, Revolution Medicines, and Revolution Medicines, based on current listings on Migrate Mate as of November 2026. Hiring at this level tends to come from manufacturers, medical device companies, defense contractors, and food and beverage producers with complex regulatory compliance requirements.
Are there remote senior level quality assurance supervisor jobs?
Yes, though remote availability at this level is more selective than in purely desk-based fields. About 22% of senior level quality assurance supervisor openings are remote or hybrid as of November 2026, with hybrid arrangements being more common since many roles require periodic on-site presence for audits, production floor oversight, or supplier visits.
What makes a quality assurance supervisor role senior level?
Senior level quality assurance supervisor roles are defined by ownership and scope. Where mid level roles execute within established systems, senior roles set quality strategy, own compliance outcomes across a facility or product line, and lead other QA staff. Expect to manage supplier quality programs, interface directly with regulatory bodies, and drive continuous improvement initiatives with cross-functional leadership visibility.
Which industries hire the most senior level quality assurance supervisors?
Senior Level quality assurance supervisor roles concentrate in Biotechnology & Pharmaceuticals, Consulting & Professional Services, and Technology & Software, based on current listings on Migrate Mate as of November 2026. These sectors drive demand because they operate under strict regulatory frameworks, such as FDA, ISO, or AS9100 standards, where experienced QA leadership is essential to maintaining certification and avoiding costly compliance failures.