In-Process Control Associate - Pharmaceutical Industry | Mitarbeiter (m/w/d) In-Prozess-Kontrolle – Pharmaindustrie

Job Summary

The In-Process Control Associate is responsible for executing critical quality assurance tasks within pharmaceutical manufacturing. Day-to-day duties include performing IPC measurements according to strict manufacturing regulations, conducting final control checks on IPC-relevant production steps, and ensuring the calibration and qualification of measurement equipment. A key component of the role involves generating and training staff on Standard Operating Procedures (SOPs), contributing to process optimization projects, and maintaining meticulous documentation compliant with GMP guidelines. Qualified candidates must hold a relevant scientific/technical qualification (e.g., Pharmaceutical Technician) or possess several years of experience in pharmaceutical production or IPC. Essential requirements include strong GMP knowledge, proficiency with laboratory software, and the ability to work independently within a required three-shift system, including occasional Saturday shifts. This role offers structured onboarding and work according to the highest quality standards.