Validation Specialist At Rameda Pharmaceutical company

 

 

 

Job Description
Participating in: GMP Projects, Different Validation Working Parties.
Checking and follow up the site validation review plans for (building, HVAC system, services and equipment).
Ensuring (under direct supervision of validation section head) that all validation activities and documentation are complying with the recommendations of guidelines as well as VMPs and product master file.
Share in preparing the Validation Master Plans (VMP) , design qualification ,installation Qualification & operation Qualification and Performance Qualification Protocols (PQPs) and Validation reports (VR) for different validation activities such as:
Process validation.
Cleaning validation.
Thermal Mapping.
Media fill.
Internal & External Calibration.
Internal & External Qualification.
Annual product quality review (APQR).
Holding Time for Pharmaceuticals during Manufacturing Process.
Following up the following activities to review and approve them:
Receiving all calibration certificates, follow its approval and filing.
Filing all validation deliverables and retrieving them professionally.
Review for all new standard operating procedure related the validation section.

Job Requirements
1-3 years of experience
Bachelor degree of pharmacy or Science

For applying Send your C.V to Engy.wasfy@rameda.com