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Project Engineer Biologics Manufacturing

Supports QA/Validation Department through preparation of design documents and protocol review. Recommends and manages implementation of appropriate corrective/preventative actions for existing equipment and manufacturing processes. Evaluates, approves, prepares, and executes change control documentation. Supports Manufacturing and Maintenance activities as technical advisor. Maintains clean and safe working environment by enforcing procedures, policies, and regulations. . Knowledge and Skills: Thorough knowledge of cGMPs and sanitary equipment design requirements. Working knowledge of process control systems and automation. Advanced knowledge of engineering documentation required for cGMP process equipment. Strong written and oral communication skills.

Iowa City, Iowa