Pharmaceutical Quality GMP Auditor (Consulting)

Advarra; United Kingdom; Híbrido; GBP 90.000 - 130.000; A tiempo parcial

Descripción de la vacante

Advarra is seeking GMP Auditors to join our consultant network. Auditors support compliance reviews across GMP sites and vendors.

Candidates should have 10+ years QA/GMP experience, 5+ years GMP auditing, and familiarity with FDA/EMA expectations. English at B2 level is required. This is a hybrid/remote role based in the United Kingdom, part-time.

Formación

• Minimum 10+ years of Quality Assurance and/or GMP experience.
• Minimum 5+ years of GMP auditing experience.
• Experience with regulatory agency expectations (FDA/EMA) and audit readiness.
• Experience developing quality assurance and audit programs; corrective actions.
• B2 level in English communication, verbal and written.

Responsabilidades

• Conduct GMP audits (planning, audits, reporting).
• Evaluate CROs and vendor compliance or qualification.
• Prepare comprehensive audit reports with findings and root causes.
• Provide corrective actions support and present findings to QA leadership.
• Collaborate with clients to ensure quality standards.

Conocimientos

GMP experience

Quality Assurance

Regulatory knowledge

English (B2)

Descripción del empleo

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Pharmaceutical Quality GMP Auditor (Consulting)

• Posted on November 6, 2026

Locations

Showing 1 location

Remote - United Kingdom

• Hybrid
• Consultant
• Part-Time
• Requisition #: PHARM004868

Description

Location

This role is open to candidates based in the United Kingdom.

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. Auditors support compliance reviews across GMP sites and vendors.

Job Duties & Responsibilities

• Conduct Good Manufacturing Practice (GMP) audits (planning, agenda, physical or remote audit, and report writing)
• Evaluate CROs, and vendor compliance or qualification.
• Prepare comprehensive audit reports detailing findings and root-causes.
• 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 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

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.