Global Clinical QA Auditor - Hybrid & Flexible Schedule

Grifols, S.A; Sant Cugat del Vallès; Hybrid; EUR 60,000 - 80,000; Full time

Benefits offered by this job

Hybrid model

Flexible schedule

Job summary

Grifols, S.A. seeks an experienced QA Auditor to plan and conduct audits of CROs, vendors, and investigator sites, ensuring compliance with applicable regulations and standards.

The role also conducts internal GCP process audits and reviews procedures for clinical audits, providing guidance to clinical staff on resolving findings. The candidate should have a PhD or Master in pharmaceuticals or life sciences, 2–3 years of GCP/GCLP QA experience, advanced English, and travel availability.

Qualifications

• PhD or Master in pharmaceuticals or life sciences related field.
• 2–3 years of practical experience in GCP and GCLP quality assurance or compliance.
• Advanced English language required.

Responsibilities

• Plan and conduct audits of CROs, vendors, investigator sites; assess compliance with regulations and standards.
• Conduct internal audits of Clinical GCP processes for SOPs, company policy, and regulations/standards.
• Review internal procedures related to planning, conduct and oversight of clinical audits.

Skills

GCP/GCLP experience

Quality assurance

Travel availability

Advanced English

Education

PhD or Master in pharmaceuticals or life sciences

Job description

Grifols, S.A. seeks an experienced QA Auditor to plan and conduct audits of CROs, vendors, and investigator sites, ensuring compliance with applicable regulations and standards.

The role also conducts internal GCP process audits and reviews procedures for clinical audits, providing guidance to clinical staff on resolving findings. The candidate should have a PhD or Master in pharmaceuticals or life sciences, 2–3 years of GCP/GCLP QA experience, advanced English, and travel availability.