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Pretoria: Quality Assurance Pharmacist (Public sector / Pharmaceutical Manufacturing) posted by Isilumko Staffing

Pretoria: Quality Assurance Pharmacist (Public sector / Pharmaceutical Manufacturing) posted by Isilumko Staffing

Posted on 2025-06-17 00:00:00

Employer Isilumko Staffing
Category Other Medical
Location Gauteng  / Pretoria

Job Summary

One of our state owned clients are in need of an experienced and registered Quality Assurance Pharmacist towards Pretoria.

Qualifications and experience:

  • B.Pharm degree or related
  • GMP training
  • Registered as a practicing pharmacist with SAPC
  • No less than 5 years’ experience in a pharmaceutical manufacturing company, no less than 3 years’ in a QA role

Knowledge:

  • ISO
  • GMP
  • QA principles

Key skills:

  • Communicate at all levels
  • Computer literate
  • Time management
  • Planning
  • Attention to detail

Key performance areas:

  • Ensuring adherence to quality management system and good manufacturing practices, ISO9001
  • Authorize product releases and recording verifications
  • Managing and controlling the process for quarantine, sample and release of products for sale
  • Review and release packaging material, raw material, intermediate products and finished goods
  • Inspection of retention samples as representatives sample of batch
  • Recommending product recalls where products do not meet specifications
  • Controlling the issuing of labels and controlled printed materials
  • Serving as a member of the change control committee
  • Implement and guide: NTP in QQA GMP and ISO principles
  • Make decisions according to approved cGMP requirements, SOP’s and / or corporate procedures and principles, within scope of Deputy Responsible Pharmacist
  • Ensure compliance to GMP, with specific reference to radiopharmaceutical products – process inspections
  • Prepare, update, review, approve procedures
  • Train on cGMP and relevant SOP and related topics
  • Maintain and ensure compliance to quality agreements
  • Prepare for and participate in management review
  • Lead or partake in risk assessments and validations activities
  • Coordinate and control the stability program
  • Preforming annual product reviews
  • Performing trend analysis of various quality parameters of products
  • Drafting monthly and quarterly reports
  • Administer continual improvement system and lead or partake in CAPA / deviation investigations
  • Establish specifications
  • Assist in conducting supplier and internal audits, preparing for audits by 3rd parties
  • Reviewing new guidelines, outside inspection reports and current trends in GMP
  • Assisting the project groups on projects, QA activities on new product development and new facilities
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