Responsible for validation activities associated with the development of new products processes systems and facilities and support of existing products process personnel regarding products equipment and processing techniques. 1. Leads execution of validation activities for both new and inline products. 2. Leads segments of technology transfer for new products CIP/SIP/process design and process equipment specification in support of validation activities. 3. Independently troubleshoots and effectively resolves manufacturing problems. Develops and implements corrective actions to unplanned (atypical) manufacturing events to ensure a consistent and reliable supply of vaccines and sterile products. 4. Contributions to planning design and implementation of segments of new or upgraded process facilities and equipment in a cost effective and timely manner. 5. Prepares and/or provides review and guidance for regulatory filings process descriptions atypical process reports and change requests. 6. Minimum of 5 years relevant experience with B.S. - minimum 3 years with M.S. or PhD.
• EDUCATION B.S./M.S./Ph.D. in Chemical Engineering or Biological Sciences.
• JOB DURATION: This job is full time and long term