Senior Quality Assurance Auditor
Celcuity - Remote
Posted Jun 4, 2026
Benefits
- Parental leave
- Not verified
- Non-birth-parent leave
- Not verified
- Family-building benefits
-
- Fertility benefits: Not verified
- Adoption assistance: Not verified
- Surrogacy assistance: Not verified
- Mental health support
- Not verified
- Relocation assistance
- Not verified
- Childcare support
- Not verified
- Learning budget
- Not verified
- Verification
- Not verified
- Salary
- $135K-$165K From the posting source
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Market context
- U.S. role benchmark (BLS OEWS)
- $106,409 U.S. median for this role
- Projected growth (BLS Employment Projections)
- +7.7% - Faster than average
U.S. benchmark only; posted salary is not compared across countries or currencies.
Matched to SOC 13-2011 - Finance aggregate by role bucket.
Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.
Role
Schedule
- Shift type
- Not verified
- Weekend work
- Not verified
Company
- Equity
- Offered Verified - SEC 10-K source
Application
- Cover letter
- Not verified
- Assessment
- Not verified
- Deadline
- Not stated
Where they hire
State eligibility is not yet verified.
About this role
Senior Quality Assurance Auditor Remote Title: Senior Auditor Location: Remote Position Summary: We are seeking a Senior Auditor who will report into the Director, Quality Assurance. The Senior Auditor is a technical expert responsible for independently planning, leading, and executing complex internal and external GxP audits across Celcuity. This role focuses on assessing and mitigating high-risk compliance issues and leading continuous improvement initiatives. The Senior Auditor plays a critical role in maintaining the highest standards of product quality, safety, and regulatory compliance. Responsibilities: Conduct vendor, investigator site, and internal audits according to applicable GxP requirements. Prepare detailed, high-quality audit reports and facilitate responses to audit observations. Support the vendor management program by performing initial audits of vendors. Manage the audit process through the quality management system. Lead or participate in strategic initiatives to continuously improve the Quality Management System (QMS), audit processes, and overall compliance to global standards. Provide guidance and training on GxP requirements to functional area personnel. Provide guidance and support during inspections and assist in developing responses to agency observations. Provide audit metrics to Executive Management. Working knowledge of regulatory requirements (FDA, EU) and related standards (GxP, CAP, CLIA). Other duties as assigned. Qualifications: Bachelor's degree in in health or life sciences; or relevant experience. 10 plus (10+) years of experience in auditing and quality management systems in pharmaceutical, biotechnology, or medical device industry in a GxP regulated environment. Relevant professional certifications such as ASQ Certified Quality Auditor (CQA) or a Lead Auditor certification are highly preferred.
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