Grand River Aseptic Manufacturing; Grand Rapids, MI; Computer Systems Validation Engineering Supervisor; prepare appropriate documentation for assigned projects in the areas of equipment, software, process, control system and critical system C & Q and validation activities; utilizes risk assessments to identify critical areas for validation and generates test scripts, and reviews change control documents, work orders, document change requests for assessing impact on validated systems; supervises staff on CSV methods and best practices; assist IT Department Head with yearly budget of CSV needs. Oversee all CSV projects to ensure timely completion on project deliverables. Bachelor's in related engineering field, information technology, or automation, plus 2 years' validation experience in API, pharma, biopharma and/or biotech manufacturing. Apply to: J. Quillen 140 Front Ave SW, Grand Rapids, MI 49504 or jquillen@grandriverasepticmfg.com{target="_blank" rel="noopener"}