Dalitso Holdings Vacancies 2022 – Apply For QA Pharmacist Jobs In Midrand, Gauteng

Website Dalitso Holdings

Key Outputs:

  • Assist with external audits were necessary; compile reports and follow-up on CAPA
  • Participate in risk assessments on QMS and departmental processes to assess risk and identify mitigating actions and controls
  • Conduct root cause investigations into incidents and deviations identifying root cause and CAPA
  • Participate in Quality Management Reviews to identify trends in QMS processes and implement CAPAs to address any deficiencies
  • Review and approve Master Batch Documents for compliance in line with the dossier
  • Review Annual Product Quality Review reports and initiate CAPA’s from the recommendation of these reviews
  • Compile, review and approve QMS SOP’s ensuring compliance to the SAHPRA cGMP Guidelines
  • Train and implement the QMS SOP’s ensuring understanding by the relevant staff
  • Review, track and follow through on change controls, deviations and assess the impact of the change and deviation on quality systems and processes
  • Perform and track internal audits / self-inspections of departments as per schedule, compile reports and follow-up on corrective and preventive action
  • Controlling and assigning expiry dates for finished products on the ERP system
  • Review Packaging Material test reports
  • Prepare monthly reports on the status of deviations, change controls, corrective and preventive action, risk assessments, and reprocesses
  • Monitor compliance with cGMP requirements in the sterile plant
  • Audit all sterile plant batch records for compliance and release
  • Participate in validation programs, including media fill
  • Review investigations arising from customer complaints, ensuring that complaints are thoroughly investigated, and effective corrective and preventative actions have been identified and implemented

Minimum Requirements:

  • Bachelor Pharmacy Degree
  • Registration with South African Pharmacy Council
  • 1 years’ Sterile experience in aseptic manufacturing
  • 2 years’ QA experience within a pharmaceutical manufacturing environment
  • cGMP skills
  • Computer Literacy: MS Office (proficient in Excel, Word, and Power Point)
  • QMS and pharmaceutical knowledge
  • Understand the requirements of the relevant Acts and regulations governing the pharmaceutical industry.


  • Deciding and initiating action
  • Leading and supervising
  • Working with people
  • Adhering to principles and values
  • Presenting and communicating information
  • Applying expertise and technology
  • Learning and researching
  • Planning and organizing
  • Following instructions and procedures
  • Adapting and responding to change
  • Coping with pressure and setbacks

To apply for this job please visit www.ditto.jobs.