Labormitarbeiter (m/w/d)
Core
Planning, preparation, execution, and evaluation of experiments for developing manufacturing processes for new parenteral drugs, specifically liquid dosage forms of biotechnologically produced active substances in vials, syringes, or cartridges, as well as lyophilisates.
Role type
Senior IC process development laboratory specialist (pharmaceuticals)
Builds
Technical batches for process and product development
Domain
Pharmaceuticals / Biotechnology / Process Engineering
Required skills
cGMP compliance, parenteral drug manufacturing processes, process development, technical batch production, equipment maintenance and calibration, scientific documentation, regulatory guidelines knowledge, statistical analysis, German (fluent), English (fluent)
Preferred skills
Master's degree or State Examination, 3+ years of experience, statistical software proficiency
Technologies
Laboratory equipment for parenteral drug manufacturing, statistical software
Responsibilities
Plan, prepare, execute, and evaluate experiments for manufacturing process development; Produce technical batches for process and product development; Support transfer of manufacturing processes to commercial sites; Maintain and calibrate laboratory equipment; Document work according to internal and regulatory guidelines; Represent work results internally and externally; Ensure compliance with all relevant occupational safety regulations.
