Fresenius Kabi Manufacturing S.A. Available Job Opportunity – Apply Now!

Managing quality within the business to achieve the quality objective reliably through a comprehensively designed and correctly implemented system of quality assurance, incorporating good manufacturing practice.

Job Title: Quality Assurance Manager
Location: Port Elizabeth, Eastern Cape, South Africa
Reference #: “QA0921
Contract Type: Permanent
Salary: 7.00 – 8.00 Annually

Job Summary:
.Ensuring the qualification and maintenance of the department, premises and equipment.
.To ensure that the required initial and continuing training of his department personnel is carried out and adapted according to need.
.The authorization of written procedures and other documents, including amendments;
.Providing a Training Management System for the training of all staff
.The approval and monitoring of contract manufacturers and providers of other related outsourced activities
.To oversee the vendor management program
.Perform GMP Compliance training (on the job)
.Provide support during Mock recall
.Responsible to conduct investigations and root cause analysis through Kabitrack
.To oversee the preparation and management of all Printed Packaging Material function in line with SAHPRA requirements
.Providing a system for the retention of records
.Management of quality systems and related standard operating practices.
.Participation in management reviews of process performance, product quality, and of the quality management system and advocating continual improvement
.Participation in external audits and inspections to ensure a positive outcome
.Responsible for Internal audits and self-inspection programs to ensure that FKMSA operates in compliance with both regulatory requirements and in-house standards, regarding Current Good Manufacturing Practice.
.Pro-active contribution in the handling of product failures and anomalies – Investigation into causes, implementation of corrective/preventive action and recording and trending of data.
.Ensure appropriate management systems are in place for data related to deviations, process deviations, trending of deviations, OOT, OOS, Root Cause Analysis, CAPA, Change Control, Risk Assessments, Customer Complaints, PQR and all other Quality data and documents. and that systems are being adhered to in accordance with GMP and Corporate standards.
.Management of customer complaints from the market ensuring they are handled effectively and efficiently. This includes, but is not limited to, the investigation into causes, implementation of corrective/preventive action and written and/or verbal response to marketing and customers. Recording and trending of complaint data and issuing of reports.
.Ensure that GMP relevant Management documents (SMF and QM handbook) are up to date, implemented and followed.
.Ensure that GMP relevant documents (SOP and Specifications) are in compliance with current GMP requirements and corporate guiding documents.
.Ensure that GMP relevant Management documents (VMP) are up to date, implemented and followed.
.Provide system for control of global Documents and related training.
.Ensure that Continuous Improvement programs for Quality Management areas
.Review and approval of annual Product Quality Reviews for all products.
.Ensure trending & statistical evaluation of GMP relevant data is performed and used for quality improvements and root cause analysis for complaints, deviations, OOT and OOS.
.Ensure that training of operators and staff is appropriately performed and efficient

Requirements:
•BSc. Micro/Chemistry/Biotechnology or B Pharm
Direct experience within the pharmaceutical sterile manufacturing environment is essential
•5-10 years of previous pharmaceutical experience within a Quality Assurance function
•Experience/ strong interest in product problem solving and product research and development
•Management experience within manufacturing environment

To Apply:

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Application Deadline: 12/10/2021