Quality Assurance Associate

About the role

Telix Pharmaceuticals is seeking a Quality Assurance Associate to support the commercial scale‑up of its radiopharmaceutical products in Europe. The role will contribute to the Group’s strategic quality goals and assist with the international roll‑out of approved imaging agents. You will work within Telix Innovations in Herstal, reporting to the Senior Quality Assurance Manager.

Key responsibilities

• Maintain GMP compliance and manage documents within the Telix Quality Management System (QMS) and eQMS.
• Participate in deviations, investigations, CAPA, change control and complaint handling.
• Conduct internal quality audits, supplier audits, and support CMOs and external vendors in line with EU GMDP and other regulations.
• Review SOPs, batch records and quality control results to ensure regulatory compliance.
• Support batch release activities for commercial and clinical products.

Required profile

• Bachelor’s degree (preferably pharmacy, biochemistry or a related science).
• At least 2 years of quality experience in a regulated industry.
• Knowledge of EU and US pharmaceutical regulations.
• Fluency in English and French.

Required skills

• Good Manufacturing Practice (GMP) knowledge.
• Experience with Quality Management Systems (QMS) and electronic QMS (eQMS).
• CAPA and deviation management.
• Understanding of EU Good Distribution Practice (GMDP).

What we offer

• Competitive salary and annual performance‑based bonus.
• Equity‑based incentive program.
• Generous vacation and paid wellness days.
• Support for learning and professional development.