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Fleet Monitoring And Inspection Officer

Job in Durban, 3611, South Africa
Listing for: EdUpStairs
Full Time position
Listed on 2026-10-12
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist - Analyst/Manager, Quality Engineering, Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist
Job Description & How to Apply Below
Quality Assurance Specialist - Pharmaceutical Manufacturing

Our client is seeking a detail-oriented Quality Assurance Specialist to join their pharmaceutical manufacturing operations in Durban . You will be responsible for ensuring that all manufactured products meet stringent quality standards and comply with regulatory requirements, including those set by SAHPRA. This role involves meticulous review of batch records, deviation investigations, change controls, and validation activities. You will play a critical part in maintaining the integrity and safety of our client's pharmaceutical products, working within a team dedicated to upholding the highest levels of quality and compliance in a fast-paced production environment.

Your expertise will be vital in supporting continuous improvement and ensuring regulatory adherence.

About the Role

Our client is seeking a detail-oriented Quality Assurance Specialist to join their pharmaceutical manufacturing operations in Durban . You will be responsible for ensuring that all manufactured products meet stringent quality standards and comply with regulatory requirements, including those set by SAHPRA. This role involves meticulous review of batch records, deviation investigations, change controls, and validation activities. You will play a critical part in maintaining the integrity and safety of our client's pharmaceutical products, working within a team dedicated to upholding the highest levels of quality and compliance in a fast-paced production environment.

Your expertise will be vital in supporting continuous improvement and ensuring regulatory adherence.

Key Responsibilities
  • Review and approve batch manufacturing records, ensuring adherence to established procedures and specifications.
  • Investigate deviations, non-conformances, and customer complaints, implementing corrective and preventive actions (CAPAs).
  • Manage and execute change control processes for manufacturing processes, equipment, and materials.
  • Participate in internal and external audits, ensuring readiness for regulatory inspections.
  • Develop and maintain quality system documentation, including SOPs, work instructions, and training materials.
Requirements
  • Bachelor's degree in Pharmacy, Chemistry, Engineering,
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