Pharmazeutischer Operator (m/w/d) Puffer- und Medienherstellung - 1-Jahresvertrag
Core
Manufacturing of media and buffers at a scale of 5–3000 liters, cleaning and sterilization of equipment, and monitoring production processes under GMP conditions.
Role type
Production operator (biopharmaceutical manufacturing)
Builds
Biopharmaceutical media, buffers, and sterile equipment for CDMO clients
Domain
Biopharmaceuticals / CDMO
Required skills
GMP compliance, process control systems, analytical measurements (pH, density, osmolality, conductivity), documentation, equipment qualification, risk analysis
Preferred skills
SAP, MS-Office, shift work flexibility
Technologies
Process control systems, CIP, SIP
Responsibilities
Manufacture media and buffers, clean and sterilize equipment, monitor production parameters, document GMP-compliant records, support qualification and validation, assist in creating batch records and SOPs
Seniority
Entry-level to Mid-level, hands-on IC
