Quality Assurance Specialist – Audits

Overview Multilingual HR Leader | 10+ Years Driving Talent Development | Strategic People Partner | Global HR Operations Expert | Workplace Architect

Join Rephine Barcelona : Elevate Quality in Life Sciences At Rephine, we are global experts in quality assurance & GxP compliance for Pharma, Biotech & Medical Devices. With offices in Spain, UK, India & China, we work with top Life Sciences companies worldwide.

Who Are We Looking For? Are you passionate about Pharma & Life Sciences? Do you thrive in team environments and enjoy managing multiple projects? If so, we want you on board as a GMP Quality Assurance Technician in Barcelona!

Your Mission You will play a key role in ensuring GMP audits are technically aligned and compliant, while supporting our expert auditors.

Responsibilities Ensure audits are prepared, executed & reported effectively.

Monitor audit life cycles and schedules.

Review audit reports to ensure compliance.

Request, review & validate CAPAs (Corrective and Preventive Actions).

Support clients with technical expertise.

Ensure confidentiality & no conflicts of interest.

Follow Quality System procedures & investigate internal incidents.

Participate in or conduct audits when needed.

Qualifications Degree in a scientific field (Pharmacy, Chemistry, Biology, Engineering, etc.).

2+ years of GMP experience in Pharma, Biotech, or Medical Devices.

Strong knowledge of FDA, EMA, ICH regulations.

Excellent communication & leadership skills.

Fluent in Spanish & English (other languages are a plus).

Ability to manage multiple projects & work independently.

Willingness to travel up to 20%.

Why Join Us? Hybrid & flexible work model, shorter Fridays.

Continuous learning (training, English & language lessons).

Global & dynamic work environment with an expert team.

Team events & social activities – because we celebrate success together!

Join a company that’s shaping the future of Life Sciences Quality.

Apply in English via our Careers Page!

Job details Seniority level : Associate

Employment type : Full-time

Job function : Quality Assurance

Industries : Pharmaceutical Manufacturing

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