Description
Telix Pharmaceuticals is hiring a Quality Control Specialist in Seneffe, Belgium, to support product development, clinical, and commercial production under cGMP. The role performs and coordinates QC inspections and tests on raw materials, packaging, intermediates, and finished products, including work with short-lived radioactive isotopes; manages laboratory materials, equipment qualification, deviations, corrective and preventive actions, and analytical validation; and supports QC procedures and ICH Q14/Q2R2 activities. Candidates need chemistry, radiochemistry, pharmacy, biochemistry, or laboratory technician education, at least three years of GMP and analytical chemistry experience, and proficiency in French and English.
