Description:
The Validation Engineer is responsible for performing validation and Engineering activities, conducting development studies, analyzation and assist in improving pharmaceutical systems and processes.
Essential Functions:
- Design, review and execute validation document activities such as Factory acceptance test (FAT), Installation qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) for equipment /utilities/facilities and generate reports which summarize results, specification and its acceptance criteria
- Performs re-qualification of equipment, facility and utilities as required
- Responsible for creating validation project and validation progress reports - weekly and monthly
- Participate in evaluation of failures and out of specification results impacting compliance with quality, safety and other design requirements
- Provide Technical Inputs and develop strategy for various domestic and international Site Transfer projects. Provide regular status updates to the department and program management.
- Closely works with the maintenance & facility teams to complete new equipment installation, commission and validation as per project requirement.
- Performs engineering assessment and writes investigation reports for non-conformance
Additional Responsibilities:
- Assists with engineering projects and performs other duties as assigned.
Amneal is an Equal Opportunity Employer that does not discriminate on the basis of sex, age, race, color, creed, religion, national origin, sexual orientation, gender identity, genetic information, disability, veteran status, liability for service in the U.S. Armed Forces or any other characteristic protected by applicable federal, state, or local laws.
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