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Gxp Auditor Jobs (NOW HIRING)

Syneos Health

Auditor I QA

Miami, FL · On-site

$47K - $79K/yr

Auditor I QA Syneos Health ® is a leading fully-integrated life sciences services organization ... Some knowledge of GCP and GxP regulatory requirements. * Knowledge of Medical and technical ...

Syneoshealth

Auditor I QA

Miami, FL · On-site

$47K - $79K/yr

Auditor I QA Syneos Health is a leading fully-integrated life sciences services organization built ... Some knowledge of GCP and GxP regulatory requirements. * Knowledge of Medical and technical ...

Kuehne+Nagel

Warehouse Quality Auditor

Piscataway, NJ · On-site

$20.60/hr

Uphold global quality standards, such as ISO, GxP, IATA CEIV What we would like you to bring * High ... auditing, ideally in logistics or contract environments What's in it for you At Kuehne+Nagel we ...

Regeneron Pharmaceuticals

Senior IT Auditor

Sleepy Hollow, NY · On-site

$99K - $130K/yr

The Senior IT Auditor is responsible for contributing towardsplanning, executing, and reporting on ... Strong understanding of SOX, COSO, COBIT, NIST,GxP, GDPR, and other relevant regulatory and ...

Jj

Pharmacovigilance QA Auditor Specialist

Horsham, PA · Hybrid

$79K - $127K/yr

Supports audits, data, internal facilities and processes in GxP/non-regulated areas * Supports ... Broad understanding of auditing process and landscape * Audit experience in various audit types ...

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How much do gxp auditor jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for gxp auditor in the United States is $19.21, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $19.23 per hour, depending on experience, location, and employer.
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Infographic showing various Gxp Auditor job openings in the United States as of August 2026, with employment types broken down into 85% Full Time, 10% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 89% Physical, 5% Hybrid, and 6% Remote job distribution, with an average salary of $39,947 per year, or $19.2 per hour.

Auditor II, Global GMP/GDP Audits & Compliance (Candidates local to RTP or Silver Spring ONLY)

Chapel Hill, NC • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Medical, Dental, Vision, Retirement, PTO

Posted 12 days ago

Job description

Responsibilities:
  • Ensure appropriate quality systems at UT sites and with approved GMP/GDP suppliers via internal audits, supplier qualification/surveillance audits, Quality Agreements support, regulatory inspection support, and assigned quality improvement initiatives.
  • Conduct initial and routine audits of QMS elements (manufacturing/packaging, facilities, distribution, analytical processes, technical reports, design history files); perform mock pre-approval inspections as needed.
  • Create risk-based audit schedules/plans; write audit reports; evaluate audit responses/corrective actions; follow up on issues and track ongoing cGMP compliance.
  • Perform internal audits across the product lifecycle (development to commercialization).
  • Assess/audit current and prospective GMP/GDP CMOs/vendors for compliance with UT standards and GMP/GDP regulations.
  • Prepare vendor risk assessments and risk control plans; review supplier quality events/change notifications to maintain product/vendor quality history.
  • Oversee the GxP Vendor List; review/approve new material part numbers and vendor requests.
  • Coordinate with internal stakeholders; assist investigations of quality issues (as directed by QA).
  • Support development projects for cGMP compliance at launch (participate in teams, train personnel, prioritize vendor qualifications).
  • Receive/assess/disseminate Vendor Change Notifications; monitor and report QMS performance.
  • Review/evaluate UT procedures for regulatory alignment; assist with initial supplier Agreements.
Minimum Requirements:
  • Bachelor’s degree in science/engineering.
  • 5+ years auditing/managing suppliers in FDA-regulated medical device/pharma environments.
  • Strong cGMP knowledge (21 CFR Parts 4, 11, 210, 211, QMSR) and familiarity with ISO/ICH.
  • Valid passport (or ability to obtain).
  • Strong attention to detail; can work independently and on multifunctional teams.
  • Strong organization/prioritization and communication (verbal/written) with internal/external stakeholders.
  • Computer skills (Microsoft Office: Word/Excel/PowerPoint).
Preferred Qualifications:
  • Master’s or PhD in science/engineering.
  • ASQ Certified Quality Auditor or ISO lead auditor; RAC-RAPS.
  • Experience auditing sterile/solid dose/biologic manufacturing.
  • Experience reviewing device development documents/Design History Files; knowledge of electronic QMS (SAP, Trackwise Digital, MasterControl).
Benefits:

Comprehensive benefits suite including medical/dental/vision/prescription coverage, wellness resources, 401(k)/ESPP, paid time off and paid parental leave, disability benefits, and more.

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