The Company
Our client is a Pharmaceuticals company and established presence in generics, we have significant innovative research and operations supporting our growing portfolio of specialty and biopharmaceutical products.

Role Description
Responsible for conducting routine validation tasks and supporting validation projects, including creating and executing commissioning, qualification, and validation protocols, performing temperature mapping, miscellaneous validation activities, and investigating and implementing corrective actions for protocol exceptional conditions.

Responsibilities
MBO level 4 with at least 6 year experience or HBO with at least 4 year experience
GMP experience in pharmaceutical or relevant industries
Validation experience
 
Requirement
Perform routine validation activities and provide support for validation projects.
Develop and execute commissioning, qualification protocols, and validation protocols (CP/IQ/OQ/PQ), ensuring identification and resolution of exceptional conditions.
Conduct temperature mapping and other miscellaneous validation tasks.
Investigate and implement corrective actions for protocol Exceptional Conditions.
Assist in coordinating validation instrument inventory calibrations and certifications.
Provide support for vendor protocol executions as needed.
Generate Computerized System Validation (CSV) documents, including computerized system Risk Assessments, Validation Project Plans, User Acceptance Tests, and Reports.

Other Information
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