QC Analyst / Quality Control Analyst / Laboratory Analyst / HPLC Analyst

SUMMARY:
A well-established manufacturing organisation is seeking a self-motivated and detail-oriented QC Analyst to join its Quality Control team.

POSITION INFO:
Job Title: QC Analyst Alternative Titles: Quality Control Analyst / Laboratory Analyst / HPLC Analyst Location: Parow, Cape Town Province: Western Cape Department: Quality Control Employment Type: Full-Time Industry: Pharmaceutical / Cosmetics / Manufacturing The QC Analyst will perform analytical and quality control testing across raw materials, packaging components, bulk product, finished goods and production processes. The role requires strong HPLC experience, sound laboratory practices and experience working with analytical equipment, deviations, OOS investigations and QC documentation. Key Responsibilities Quality Control Testing Perform line opening checks in primary and secondary production areas. Ensure compliance with SOP requirements before filling and packaging. Test and inspect raw materials. Test packaging components. Test bulk product. Test finished goods. Conduct in-process control checks. Test water samples and report out-of-specification results. Analytical Testing Perform HPLC analysis. Prepare and standardise chemical solutions. Operate analytical QC equipment. Verify instrument status before use. Confirm calibration status. Report calibration deviations. Maintain analytical equipment in good working condition. Ensure QC equipment remains fit for purpose. Laboratory Equipment Operate equipment including: HPLC pH meters Viscometers Scales Ultrasonic bath Microscope Melting point meter Label printer Outsourced Testing Prepare samples for outsourced testing. Send samples to external service providers. Verify returned results. Analyse results against procedures and specifications. Documentation & Reporting Complete and sign analytical records. Maintain accurate testing documentation. Recommend updates to documents where required. Prepare analytical reports on deviations. Maintain retained samples in controlled conditions. Ensure documentation is accurate and complete. Deviations & Corrective Actions Identify deviations. Investigate out-of-specification results. Assist with deviation resolution. Support corrective action implementation. Investigate customer complaints. Recommend changes to procedures and records. Generate supplier complaints where non-compliance is identified. Additional QC Responsibilities Prepare microbiological samples where required. Conduct year-end stock counts. Set packaging quality standards. Check filling and packing reports against production plans. Support artwork and packaging approval processes. Minimum Requirements Grade 12. National Diploma in Analytical Chemistry or related degree. Relevant BSc qualification accepted. 3-5 years' HPLC experience. Minimum 1 year's lab analyst experience. Pharmaceutical, cosmetic or related industry experience. Strong analytical equipment experience. Microsoft Office proficiency. Excellent attention to detail. Strong organisational ability. Able to work under pressure. Good written and verbal communication skills. Skills & Competencies HPLC analysis. Analytical testing. Quality Control. Laboratory equipment operation. Deviation investigation. OOS investigation. Analytical reporting. Calibration awareness. SOP compliance. Documentation control. Problem solving. Attention to detail. Prioritisation. Communication.