Quality Coordinator - Cape Town
Salary Negotiable
Cape Town,
Western Cape
more than 14 days ago
A leading Pharmaceutical company is looking for an above average Quality Coordinator to join their progressive team of highly skilled individuals. If you are looking for a progressive environment, and a company at the top of their game in the Pharmaceutical industry then, this position will suit you well!
Requirements
Minimum of 1-3 years’ work experience in a quality control, quality assurance or pharmaceutical industry
Relevant qualification
Document management experience
Experience with lot releases, PQR’s and SOP’s
High computer literacy enable to effectively use Excel
Up to date knowledge of validation, GMP and GLP (Good Manufacturing Practice / Good Lab Practice)
Up to date knowledge of validation, GMP and GLP (Good Manufacturing Practice / Good Lab Practice)
Sound knowledge of most recent analytical laboratory techniques, packaging analysis, in-process requirements and production controls
Highly accurate / attention to detail JOB SPECIFICATION Create, review and update Lot Release Forms per product Coordinate the sampling of incoming goods at the contract distributor and/or packer Coordinates the analytical reference standards at the various contract laboratories Coordinate the testing for post importation requirements and documentation thereof with contract laboratories Compile and maintain the samples register Liaise with Third party contractors Coordinate, compile and review all batch documentation relating to the lot release of all products - manufacturing, packaging and analytical records - in compliance with registered dossiers Performs Bulk material inspections before packaging and liaise with contractors, maintain registers Performs final packed product inspection, maintains the product trend charts and updates the lot release summary for all products on an ongoing basis Coordinates the timeous final product release to market of all products by the Finished Product Release Pharmacist Ensuring starting materials and bulk products are promptly released Complaints Deviations and Root Cause Analysis Training Conducts training and presentations when the need arises Audits Standard Operating Procedures Product Quality Reviews Stability General
Requirements
Minimum of 1-3 years’ work experience in a quality control, quality assurance or pharmaceutical industry
Relevant qualification
Document management experience
Experience with lot releases, PQR’s and SOP’s
High computer literacy enable to effectively use Excel
Up to date knowledge of validation, GMP and GLP (Good Manufacturing Practice / Good Lab Practice)
Up to date knowledge of validation, GMP and GLP (Good Manufacturing Practice / Good Lab Practice)
Sound knowledge of most recent analytical laboratory techniques, packaging analysis, in-process requirements and production controls
Highly accurate / attention to detail JOB SPECIFICATION Create, review and update Lot Release Forms per product Coordinate the sampling of incoming goods at the contract distributor and/or packer Coordinates the analytical reference standards at the various contract laboratories Coordinate the testing for post importation requirements and documentation thereof with contract laboratories Compile and maintain the samples register Liaise with Third party contractors Coordinate, compile and review all batch documentation relating to the lot release of all products - manufacturing, packaging and analytical records - in compliance with registered dossiers Performs Bulk material inspections before packaging and liaise with contractors, maintain registers Performs final packed product inspection, maintains the product trend charts and updates the lot release summary for all products on an ongoing basis Coordinates the timeous final product release to market of all products by the Finished Product Release Pharmacist Ensuring starting materials and bulk products are promptly released Complaints Deviations and Root Cause Analysis Training Conducts training and presentations when the need arises Audits Standard Operating Procedures Product Quality Reviews Stability General
Recruiter: CME Recruitment2