| Job Location | Obour City, Cairo , Egypt |
| Education | Not Mentioned |
| Salary | Not Mentioned |
| Industry | Other Business Support Services |
| Functional Area | Not Mentioned |
Prepares, writes and reviews validation protocols and documentation to ensure compliance and adherence to cGMP and GLP.Oversees and coordinates the timely calibration and re-validation of manufacturing equipment and instruments.Interface with Engineering, Manufacturing, Facilities, and Quality Assurance to address deviations from the norm, out of tolerances and potential product concerns related to maintenance, calibration, or re-validation issues, define and implement effective corrective actions and monitor post-implementation effectiveness.Works with calibration and validation service providers (vendors/contractors) to coordinate work. Ensures external calibration contractors complete work as required, on-time and with the correct standards., also responsible for external service provider?s evaluation systemMaintain and update equipment records in accordance with quality systems requirements.Ensures that all equipment files, documentation and associated databases are kept up to date as part of the calibration/re-validation program.Designs and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of equipment/instruments and prepares documentation for inspection testing procedure.Audits all new equipment documentation manuals to ensure that they are accurate and satisfactory to support operation, maintenance and instruments calibration activities.Oversees implementation of the validation programs. Ensures new equipment are properly validated prior to start up and critical equipment is periodically re-validated.
Keyskills :
Maintenance Pharmaceuticals Vetting Calibration
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