Pharmaceutical Quality GMP Auditors (Consulting)
Advarra, Inc.Japan
Posted March 17, 2026
Part Time
About the Company
Advarra seeks to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced.
Job Description
Advarra is seeking Good Manufacturing Practice (GMP) Auditors to join our consultant network for Japan-based projects. Auditors support compliance reviews across GCP clinical sites and vendors.
Requirements
- Minimum 10+ years of Clinical Quality Assurance and/or Good Manufacturing Practice (GMP) experience.
- Minimum 5+ years of Good Manufacturing Practice (GMP) auditing experience.
- Demonstrated experience with regulatory agency expectations (e.g., FDA, EMA) and audit readiness activities.
- Demonstrated experience in developing and implementing quality assurance plans, audit programs, and corrective action plans.
- B2 level in English communication, verbal and written
- B2 level in Japanese communication, verbal and written
- Bachelor's degree
Benefits
- Employee relocation not specified
