Senior Pharmaceutical Quality Control Analyst

Our client, a renowned pharmaceutical company, is seeking a highly skilled Senior Pharmaceutical Quality Control Analyst to join their state-of-the-art laboratory in Nelspruit, Mpumalanga . This role is crucial for ensuring the quality and integrity of raw materials, in-process samples, and finished pharmaceutical products. You will perform a wide range of analytical tests, interpret results, and contribute to the maintenance of a robust quality control system.

This hybrid position allows for on-site laboratory work coupled with some flexibility for data analysis and reporting from home. The ideal candidate will possess a strong foundation in analytical chemistry and a commitment to upholding the highest quality standards in pharmaceutical manufacturing within the Nelspruit region.

• Perform a variety of analytical tests on raw materials, intermediates, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
• Analyze test results, interpret data, and prepare accurate and comprehensive Certificates of Analysis (CoA).
• Ensure compliance with current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines.
• Operate and maintain laboratory equipment, ensuring proper calibration and qualification.
• Troubleshoot analytical methods and equipment malfunctions, implementing corrective actions as needed.
• Participate in method validation and transfer activities.
• Review and approve laboratory records and documentation for accuracy and completeness.
• Contribute to internal audits and support regulatory inspections.
• Maintain a clean and safe laboratory environment.
• Assist in the training of junior QC analysts.

• A Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
• Minimum of 5 years of experience as a Quality Control Analyst in the pharmaceutical industry.
• Extensive hands-on experience with analytical instrumentation such as HPLC, GC, and dissolution apparatus.
• Strong understanding of cGMP and GLP principles.
• Proficiency in data analysis, interpretation, and documentation.
• Excellent attention to detail and accuracy.
• Good problem-solving and troubleshooting skills related to analytical testing and instrumentation.
• Effective communication and interpersonal skills.
• Ability to work effectively both independently and as part of a team.
• Familiarity with laboratory information management systems (LIMS) is advantageous.

Our client provides a competitive salary and a comprehensive benefits package, including medical insurance, retirement fund contributions, and paid time off. This hybrid role offers the flexibility to balance on-site lab work in Nelspruit with remote data analysis. Opportunities for professional development and career advancement within the company are available. Join a dedicated team committed to ensuring the highest quality standards in pharmaceutical products.