Manufacturing Associate (level III)

Proclinical is looking for a Manufacturing Associate (Level III) to join its pharmaceutical production site, where the focus is on delivering high‑quality medicines under current Good Manufacturing Practice (cGMP) standards. In this hands‑on role you will carry out and record daily manufacturing tasks, run process equipment, follow validation procedures, keep cGMP documentation up to date, and maintain the equipment and facilities to required conditions while assisting other on‑site functions as needed. The position requires a strong eye for detail, solid documentation abilities, and familiarity with cGMP regulations and manufacturing processes. You must be capable of operating and servicing production equipment and be willing to work collaboratively with cross‑functional teams. Candidates need the legal right to work in the location or an EU passport. A collaborative mindset and a commitment to compliance and quality are valued.