Pharmaceutical Quality GMP Auditors (Consulting)
- Status
- Open
- Remote policy
- Remote
- Employment type
- Not stated
- Salary
- Not stated
- Categories
- GMP-Auditor, Quality-Auditor, Pharmaceutical-Quality-Auditor, Compliance-Auditor, Consultant, Pharmaceutical-Compliance-Auditor, Pharmaceutical-Auditor, GMP-Auditing, GMP-Compliance-Consultant, Pharmaceutical-QA, GxP-Auditor, Pharmaceutical-Quality-Assurance, Pharmaceutical-Consulting
- Tech
- gcpremote-countryqa
- Source
- himalayas
- First observed
- 2026-10-21 22:04 UTC
- Last seen
- 2026-10-21 22:04 UTC
- Source claims posted
- 2026-10-21 21:59 UTC
- Consecutive misses
- 1 of 10
What the posting says
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Location
This role is open to candidates based in Japan.
Company Information
At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each person is not only valued but empowered to thrive and make a meaningful impact.
Company Culture
Our people--both employees and consultants—are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives.
Job Overview Summary
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.
Job Duties & Responsibilities
Conduct Good Manufacturing Practice (GMP) audits (planning, agenda, physical or remote audit, and report writing)
Evaluate investigator sites, CROs, and vendor compliance or qualification.
Prepare comprehensive audit reports detailing findings and root-causes.
Provide written audit reports in English.
If required will provide corrective actions support and present findings to QA leadership and stakeholders
Work collaboratively with clients to ensure quality standards.
Basic Qualifications
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
Preferred Qualifications
Strong interpersonal and client interaction skills.
Excellent analytical, problem-solving, communication, and report-writing skills.
Ability to work collaboratively across departments and interact with internal and external stakeholders.
Originally posted on Himalayas
Quality
- x Salary range stated weight 35%
- + Remote policy stated weight 20%
- + Location stated weight 15%
- + Organisation stated weight 15%
- + Publication date stated weight 15%
Not enough history yet to judge honesty signals.
Timeline
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#1469236 2026-10-21 22:04 UTCPublished
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o
#1470436 2026-10-22 00:04 UTCNot seenMiss 1 in a row