GROUP QUALITY ASSURANCE PHARMACIST
AI DMD: MIDRAND
Reporting to
Contract Manufacturing Manager, GQA
Job Purpose:
To review, approve and monitor all quality assurance activities at SA and international contract manufacturers ensuring compliance to cGMP requirements
Required Learning/experience
Key Job Outputs
B. Pharmacy, cGMP skills
Computer Literacy: Ms Office
3 years in Pharmaceutical manufacturing environment
2 -3 years Quality Assurance experience
Reviewing and approval of all master production and quality documentation for the Companys products.
Compiles and reviews SOPs ensuring compliance to required Guidelines.
Participates in audits conducted by GQA Auditor/s and regulatory
authorities on contract manufacturers and follow up on CAPA.
Review and approves all change controls and deviations initiated by
contract manufacturers for the Companys products.
Review and approves all investigations and CAPA initiated at contract
manufacturers relating to manufacturing, customer complaints, stability,
OOS and recalls.
Monitors validation and technical transfer batches at contract
manufacturers.
Performs QA release on the Companys products to the market.
Investigates and responds to all product/process queries timeously.
Participates in projects, product launches, product transfers ensuring
quality activities are completed timeously.
Manages the stability schedule and process for products
manufactured at contract manufacturers
Conducts quality reviews of operations at contract manufacturing sites
to identify continuous improvement actions
Implement adequate measures for all quality systems
Core Competencies
Basic QMS and Quality assurance pharmaceutical knowledge
Working knowledge and understanding of various pharmaceutical
approved guidelines
Proactive
Attention to detail
Good interpersonal skills team player
Deadline driven
Self-motivated
Problem solving
Good communication and presentation skills