About the Role

RRxCo are expanding our global auditor network and seeking experienced

GCP Auditors

to deliver high-quality, risk-based audits across the pharmaceutical and life sciences sector.

This role involves conducting

remote, onsite, and questionnaire-based audits , supporting clients across Europe (Spain, Portugal etc.) in meeting regulatory requirements.

What You’ll Be Doing Audit Preparation

Develop audit agendas from pre-qualification data

Align scope with RRxCo and client stakeholders

Coordinate audit logistics with auditees and clients

Review key quality and compliance documentation

Audit Delivery

Conduct

GCP audits

of investigator sites, Clinical Systems (QMS, TMF etc.), CROs and other Vendor audits.

Perform audits onsite, remotely, or via desktop assessment

Assess compliance against but not limited to:

FDA, MHRA, EMA Regulations





21 CFR part 11

21 CFR part 16

Protection of Human Subjects

21 CFR part 312

21 CFR part 314

Reporting

Deliver draft audit reports within 5 working days

Participate in debriefs where required

Finalise clear, high-quality audit reports addressing all feedback

What We’re Looking For

Expert knowledge of

Global GCP regulations

Ability to work independently and manage general stakeholders

Experience with

remote and international audits

Willingness to travel globally when needed

Why Join RRxCo?

Work with a

global client portfolio

Be part of a trusted network of

GxP experts

Opportunity to support impactful compliance initiatives worldwide

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