Validation Specialist - Sharqia
Sekem -
Belbes, SharqiaPosted 4 years ago28Applicants for1 open position
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- 0In Consideration
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Job Details
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Job Description
- Performs activities associated with Equipment IQ, OQ, PQ's and Calibrations, Validation Protocols and Reports.
- Writes Validation Protocols and Reports.
- Support Equipment Qualifications and Calibrations.
- Plan and coordinate cleaning, manufacturing processes, facilities and equipment validation activities.
- Support cleaning evaluations and verification.
- Develop validation plans and schedules.
- Coordinate validation activities with heads of departments.
- Assess regulatory impact of deviations, changes to equipment and Batch records, materials and calibrations from validation perspective.
- Analyze data and work with Project Manager to solve technical problems.
Job Requirements
- 2-3 years experience in a pharmaceutical GMP environment