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In-Process Quality Coordinator

1 week ago

Randburg, Gauteng, South Africa Aspen Pharma Group Full time

Aspen Pharma Group is a leading player in the pharmaceutical industry, and we are committed to delivering high-quality products to our customers. We are currently seeking an In-Process Co-Ordinator to join our team, who will play a critical role in ensuring the quality of our products.

The ideal candidate will have a broad working knowledge of concepts, terminology, and specialized reporting requirements, and will be able to communicate effectively with internal stakeholders to achieve work objectives.

Responsibilities:

In-Process Testing and Reporting

  • Perform in-process testing, sampling, and interpreting results.
  • Record defect, out of specification results, and reporting these as appropriate.
  • Complete required documentation, update and maintain databases, and appropriate reports.
  • Ensure that all documentation adheres to signing protocols.
  • Handle, operate, maintain, and calibrate equipment according to SOPs.
  • Comply to GMP/GLP requirements at all times.

Reporting and Record Keeping

  • Gather and record information, statistics, and evidence required for reporting.
  • Compile standardized reports and consolidate documents.
  • Retrieve supporting documentation and records to facilitate and support query resolution.

Education and Qualifications

  • Grade 12
  • 1 to 3 years' pharmaceutical manufacturing experience