QASME
Aspen Pharma Group
2026/10/06   Gqeberha

Job Ref #: QASME24082026
Industry: Production
Job Type: Permanent
Positions Available: 4
Applications are invited for the above indicated vacancy that exists at the Gqeberha site. The successful incumbent will report to the QA Manager. All applications are to be received on or before 28 August 2026. Preference will be given to Employment Equity candidates in line with Aspen’s Transformation Agenda.
Job Description

Provide Quality Assurance oversight across manufacturing operations to ensure compliance with GMP, regulatory requirements, quality standards and approved product requirements. Support quality systems, investigations, risk management and continuous improvement.

Job Requirements
  • Provide QA oversight of manufacturing, packaging, storage and distribution activities.
  • Ensure ongoing compliance with GMP, regulatory and company quality requirements.
  • Conduct GMP walkthroughs, audits and compliance assessments.
  • Lead and approve investigations, including deviations, OOS/OOT, complaints and quality incidents.
  • Review and approve CAPAs and monitor their effectiveness.
  • Identify and manage quality and compliance risks.
  • Monitor and trend quality data to identify recurring issues and emerging risks.
  • Conduct regulatory and GMP gap assessments and implement improvement plans.
  • Support regulatory, customer and internal inspections and audits.
  • Review and approve GMP-related change controls and assess quality and regulatory impact.
  • Drive continuous improvement to strengthen compliance, reduce recurring quality issues and improve inspection readiness

Qualification:

  • Bachelor's Degree in Pharmacy

Experience: 

  • 5–8 years' experience in a pharmaceutical manufacturing quality environment.
  • 2–3 years' leadership experience.