Description
The role manages production-process deviations and analytical-method deviations, reviews batch records, prepares product-specification and batch-release documentation, supports customer and regulatory inspections, and coordinates shipment and master-batch-record activities. It requires a degree in Pharmaceutical Chemistry and Technology (CTF), Biotechnology, or a similar field, at least two years of experience in sterile product manufacturing, analytical skills, proactivity, and good English knowledge. The salary range is €34,000–€38,000.
