API Manufacturing Technician
Eurofins Scientific
You will be part of a multi-disciplinary team responsible for the Current Good Manufacturing Practices (cGMP) production of non-commercial size clinical batches supporting Active Pharmaceutical Ingredient (API) development. This includes but is not limited to: supporting the manufacturing operations team, reviewing Standard Operating Procedures, executing batch records, and supporting commissioning and qualification of process equipment. Standard work will involve chemical synthesis of API, which includes these operational tasks: solid / liquid charges to vessels, atmospheric / vacuum distillations, liquid-liquid extractions, phase cut, crystallization, filtrations and drying. ROLE RESPONSIBILITIES Execute Process Operating Instructions in a cGMP {part of Gx. P} environment. Responsible for equipment preparation, operational adjustment, process monitoring, sampling, and equipment cleaning of complex pharmaceutical manufacturing equipment as defined in standard operating procedures. Per...Manufacturing Technician, Technician, Manufacturing, Operations, Equipment, 2nd Shift
Vacancy posted 3 days ago
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