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The Manufacturing Associate I is in charge of producing therapeutic proteins (API) in accordance with current Good Manufacturing Practices (cGMP) conditions. Level I associates are encouraged to complete process recipes, adhere to written Standard Operating Procedures (SOPs), supervise equipment and processes, independently carry out laboratory tasks, including pH, conductivity testing, product sampling, and perform regular sanitization tasks to uphold facility and equipment cleanliness. They are encouraged to showcase a solid grasp of cGMP compliance while working under supervision, and aseptic technique in product and material handling.