Quality Control Analyst - Pharmaceuticals

About the Role

Our client is seeking a meticulous Quality Control Analyst to join their laboratory team in Nelspruit . You will perform a variety of analytical tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet established quality specifications and regulatory standards. This role requires a strong understanding of analytical chemistry techniques and a commitment to maintaining the integrity and safety of our pharmaceutical products. You will be an integral part of ensuring compliance with Good Manufacturing Practices (GMP) .

Key Responsibilities

• Conduct routine and non-routine analytical testing of raw materials, intermediates, and finished products using validated methods.
• Perform laboratory procedures such as chromatography (HPLC, GC), spectroscopy (UV-Vis, IR), and titration.
• Accurately record and document all testing results, ensuring compliance with laboratory procedures and GMP.
• Calibrate and maintain laboratory equipment, ensuring proper functioning and adherence to schedules.
• Prepare analytical reports and certificates of analysis.
• Investigate out-of-specification (OOS) results and deviations, assisting in root cause analysis.

Requirements

• Bachelor's degree in Chemistry, Pharmacy, or a related science discipline.
• Minimum of 2 years of experience as a Quality Control Analyst in the pharmaceutical industry.
• Proficiency in analytical techniques such as HPLC, GC, UV-Vis, and Karl Fischer titration.
• Knowledge of GMP and laboratory best practices.
• Strong attention to detail and accuracy in data recording and analysis.
• Ability to work effectively both independently and as part of a team in the Nelspruit laboratory.

Benefits

• Competitive annual salary with potential for overtime pay.
• Comprehensive medical and pension benefits.
• Opportunities for on-the-job training and skill development in analytical methods.
• A structured and safe laboratory environment.
• Collaborative team atmosphere within a well-established pharmaceutical company .

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