Quality Assurance Specialist – ATMP CDMO

About the role

We are seeking a 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 compliance with GMP standards and support the delivery of advanced cell and gene therapies.

Key responsibilities

• Support GMP quality systems and maintain compliance across the organization.
• Review and manage 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 drive process improvements.
• Promote a strong quality culture and contribute to continuous improvement of quality systems.

Required profile

• Scientific background (Biotechnology, Biology, Pharmacy, Chemistry, Biomedical Sciences or related).
• Some experience in Quality Assurance, preferably in a GMP environment.
• Strong problem‑solving mindset, proactive and adaptable.
• Team‑oriented, eager to learn and take ownership.
• Positive attitude and willingness to contribute to a growing organization.

Required skills

What we offer

• Opportunity to work at the cutting edge of ATMP manufacturing.
• Young, motivated and supportive team environment.
• Exposure to a wide variety of innovative projects.
• Professional growth alongside a rapidly developing company.
• Relocation support for successful candidates.