QA Specialist
2 days ago
Our client in Cape Town, looking for a QA Specialist to join a leading pharmaceutical organization **in Lesotho on a 2 year contract.**
The objective is to produce Dronabinol API under EU-GMP conditions for distribution in Germany, Poland and the UK.
**Responsibilities**:
- Write, review and approve quality documents, including batch documents, SOPs and Quality Control documents.
- Review and approve procedural and process change controls.
- Manage non-conformance, OOS and deviations
- Conduct root cause analysis and raise/ implement CAPAs
- Support/ lead internal audits and suppler audits
**Must Have**:
- Previous experience working as a QA officer in either the Pharmaceutical, Medical Device, Biotechnology, Life Sciences or Specialty chemicals industry.
- Experience working in a GMP environment along with experience in some of the following - Deviations, CAPA, Audits, QMS or batch release.
**Job Types**: Full-time, Temporary
Contract length: 24 months
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