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Work Schedule
Standard (Mon-Fri)Environmental Conditions
Office
Job Description

Competitive sign-on bonus considered for qualified candidates

Position: We are actively hiring experienced GCP QA Auditors Level III and above

Locations: Spain, UK and France (remote) Candidates must be located in one of these countries and hold the legal right to work.

Join us as a GCP Quality Assurance Auditor III/Manager and enhance our clinical auditing processes by ensuring regulatory compliance and quality standards.

What You’ll Do:
• Conduct and/or lead a variety of client, internal or GCP audits and regulatory inspections as requested by senior management
• Perform directed site audits, facility, vendor and/or sub-contractor audits
• Provide GCP consultation and support to project teams and external clients




• Lead process audits and may participate as a co-auditor in more complex system audits
• Perform other types of QA audits or activities (e.g. database audits, clinical study report audits, sample results tables, process improvement)
• Serve as a knowledgeable resource to operational departments on audit or quality assurance subject matter
• Prepare and present audit findings and/or other related information at departmental, internal operations or client meetings
- Travel will be required, up to 12-15 times per year (on average 1-2 times per month) across EMEA

Essential Experience:
- GCP Auditing
- Investigator Site Audits

Other:
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous QA experience that provides the knowledge, skills, and abilities to perform the job (comparable to 3+ years’).

In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be

📌 QA Auditor III (España)
🏢 Thermo Fisher Scientific
📍 España