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 global stakeholders
Experience with
remote and international audits
Willingness to travel globally when needed
Why Join RRxCo?
Work with a
integral client portfolio
Be part of a trusted network of
GxP experts
Opportunity to support impactful compliance initiatives worldwide
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📌 Gcp Auditor (España)
🏢 RRxCo.™
📍 España