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Senior validation specialist - pharmaceutical industry

Cork
beBeeValidation
Validation specialist
Posted: 7h ago
Offer description

Key Responsibilities Job Summary:This position is responsible for leading and coordinating CQV activities in alignment with the site’s project strategy. Close collaboration with various functions such as Process Engineering, Operations, Engineering, Quality, EHS, Logistics, and Lean & Digital is required to understand requirements and develop an effective validation strategy. 1. Guide CQV activities ensuring timely execution and compliance with industry regulations. 2. Develop review approve commissioning installation qualification protocols managing issues efficiently according site/project procedures.
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