Quality Assurance (QA) Specialist – ATMP CDMO

About the role

We are seeking a motivated Quality Assurance (QA) Specialist to join our fast‑growing ATMP CDMO in Andorra. You will work closely with production, quality control and R&D teams to ensure GMP compliance and support the delivery of advanced cell and gene therapy products.

Key responsibilities

• Support GMP quality systems and maintain compliance across the organization.
• Review and update documentation, quality records, and equipment registers.
• Assist with GMP validations, qualifications, deviations, CAPAs, change controls and investigations.
• Collaborate with cross‑functional teams to solve problems and improve processes.
• Help sustain a strong quality culture and contribute to continuous improvement of quality systems.

Required profile

• Scientific background (Pharmacy, Biotechnology, Biology, Chemistry, Biomedical Sciences or related).
• Experience in Quality Assurance, preferably in a GMP environment.
• Strong problem‑solving attitude, proactive mindset and willingness to learn.
• Team‑player who enjoys collaborating across functions.

Required skills

• Good knowledge of GMP regulations and practices.
• Experience with quality management systems and documentation review.
• Familiarity with validation, qualification, deviation handling and CAPA processes.

What we offer

• Opportunity to work at the cutting edge of advanced therapies.
• Young, supportive team and exposure to diverse projects.
• Professional growth in a rapidly developing company.
• Relocation support for successful candidates.