Manufacturing Tech III

Role: Manufacturing Technician III supporting complex biopharmaceutical manufacturing processes in a cGMP environment, primarily involving aseptic processing, formulation, hydration, and equipment operation within biologics production. Objectives include maintaining compliance with SOPs, batch records, and quality standards while executing routine to moderately complex tasks like equipment setup, cleaning, sterilization, and manual handling of products. Responsibilities encompass aseptic processing, equipment assembly/disassembly, sterilization, process operation, and documentation, with an emphasis on troubleshooting and process adherence. Requirements include 3+ years of relevant experience, a high school diploma or GED, and prior cGMP industry exposure. Skills needed are knowledge of SOPs, batch records, and proficiency in Microsoft Office; ability to follow instructions and train others is valued. Preferred qualifications include experience with multiple manufacturing processes such as filling, formulation, or hydration. High-value biopharma specifics involve biologics, aseptic techniques, cleanroom operations, and compliance with cGMP standards. The role reports to a Team Lead and involves working in a cleanroom manufacturing setting, with no specified travel requirements.