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Specialist, MSEO Manufacturing Systems Validation
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- Our client, a leading pharmaceutical company, is hiring a MSEO Manufacturing Systems Validation Specialist on a contract basis.
- The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing.
- The Specialist will partner with site Business Owners, CI Owners, Quality, and the global EMES team to create, manage, and improve computerized systems/Recipes validation deliverables for electronic systems, applications, and associated controls to maintain data integrity supporting ALCOA+ principles throughout the CSV lifecycle.
- The Specialist will be responsible for ensuring the validation of the S12 Enterprise Manufacturing Execution System (EMES), and applications are done following the relevant company procedures, such as CSV SOP but no limited and applicable health authority regulations.
- 2 years relevant work experience required preferably in a pharmaceutical manufacturing environment.
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