Important animal health pharmaceutical laboratory
* Responsible for ensuring the GMP- and regulatory conform production of medicinal drugs acc. to guidelines e.g. EU-GMP-Guideline…
* Review the technical content of SOPs for manufacturing and Quality Control.
* Supports the GMP conform process optimization in manufacturing and Quality Control.
* Quality review of batch documentation for release purposes
* Maintaining of the OOS-/ Deviation system in the company
* Maintaining of the Complaint system in the company
* Compiles the Deviation Reports together with other Departments
* Pharmaceutical assessment of deviations and ensuring of appropriate CAPAs
* CAPA-management together with other departments
* Maintain SOP´s updated, create new ones if needed and propose improvements to existing ones.
* Maintain the Qualification / Calibrations System updated, coordinating tasks with other departments.
* Coordinates and accompanies validation activities in manufacturing and Quality Control
* Preparation of Validation Protocols in-time
* Co-operation and participation in audits and subsequent measures
* Coordinate the necessary IT validations
* Release of batches according GMP rules
Para completar tu candidatura, Page Personnel necesita completar tu registro en su web.