Quality Assurance Specialist – Audits

Rephine; Barcelona; Presencial; EUR 40.000 - 50.000; Jornada completa

Descripción de la vacante

Rephine in Barcelona is seeking a GMP Quality Assurance Technician to ensure compliance in audits while supporting expert auditors. The role includes managing multiple projects and requires a degree in a scientific field along with relevant experience in Pharma or Biotech. Join a dynamic team focused on quality assurance and enjoy competitive benefits including continuous learning opportunities.

Servicios

Competitive salary + bonus

Extra vacation days

Continuous learning (training, language lessons)

Formación

• 2+ years of GMP experience in Pharma, Biotech, or Medical Devices.
• Fluent in Spanish & English; other languages are a plus.
• Strong knowledge of FDA, EMA, ICH regulations.

Responsabilidades

• Ensure audits are prepared, executed & reported effectively.
• Monitor audit life cycles and schedules.
• Review audit reports to ensure compliance.

Conocimientos

Quality Assurance

GMP Compliance

Communication

Leadership

Project Management

Educación

Degree in scientific field (Pharmacy, Chemistry, Biology, Engineering)

Descripción del empleo

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 an 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.

What You’ll Do

• 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.

What You Bring

• 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?

Competitive salary + bonus + extra vacation days & benefits.

Continuous learning (training, English & language lessons).

Quality Assurance Specialist • barcelona, Spain