Production, cGMP, SOP and/or analytical instrumentation • Operates, maintains and calibrates automated and semi-automated manufacturing equipment. • Lead, organize and train local team members on the technological transfer of production processes (synthesis). • Contribute to the production • Initiate Investigations, CAPAs, Deviation and Change Control as related to manufacturing. • Provide related training to other staff members as required. • Participate to the qualification/validation campaign for new radiopharmaceuticals implementation according to GMP standards. • Maintain a clean and safe working environment in compliance with safety and pharmaceutical regulation. • Perform radiation safety duties in compliance with regulations. • Efficiently comply with waste management rules and regulations. EDUCATION AND/OR EXPERIENCE: Bachelor’s degree in Chemistry. • Experience in production is highly desirable. • Expertise in laboratory procedures • Read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. • Knowledge of basic cGMP requirements, practices and procedures
Do you have a strong analytical chemist background in the pharmaceutical industry with strong cGMP, SOP, QC and QA experience? Are you ready for new career development and growth? Come join a growing company in the specialty Pharmaceutical Industry and define your own career!