Responsibilities: Maintains all qualified and validated equipment and systems in compliance with policies, guidelines and procedures. Support Lifecycle Document Management System. Develops protocols, and associated reports while adherin...
Position Overview: The CSV Engineer supports the successful implementation of manufacturing and laboratory equipment and computerized systems at multi-use sites through interaction with internal customers and external service providers. Th...
Roles & Responsibilities: 3+ years of experience in the Pharma and/or Consumer Health industry. Strong understanding of regulatory requirements and industry standards. Previous experience in Document Management systems (e.g., Veeva...
Responsibilities: Execute the historical performance review (HPR), a periodic review of equipment performance and use. Compile data gathered from HPR and use to analyze trends that could show equipment failure or out of trend. Review eq...
Position Summary: Responsible for the creation and execution of computer system validation document as well as providing operational support and guidance related to system use and improvement. Responsibilities: Create and execute comput...