Senior Pharmaceutical Analyst - Raw Material Testing

Our client, a reputable pharmaceutical company, is seeking a dedicated Senior Pharmaceutical Analyst to join their Quality Control laboratory. This position is based in Klerksdorp, North West , and focuses on the rigorous testing of raw materials used in pharmaceutical manufacturing. The successful candidate will be responsible for ensuring that all incoming materials meet strict quality specifications and regulatory requirements before being released for production.

This role requires a meticulous approach, strong analytical skills, and a thorough understanding of pharmacopeial standards and analytical instrumentation. You will be a key player in maintaining the integrity and quality of our client's pharmaceutical products. We are looking for a detail-oriented professional who is passionate about ensuring the highest standards of quality in pharmaceutical ingredients.

Perform comprehensive testing of raw materials, excipients, and packaging components using various analytical techniques (e.g., HPLC, GC, UV-Vis, FTIR, KF Titration). Interpret test results, evaluate data against specifications, and make decisions on material acceptance or rejection. Prepare and review analytical test methods, validation protocols, and reports. Maintain laboratory equipment, perform calibrations, and ensure compliance with Good Laboratory Practices (GLP) and GMP.

Troubleshoot analytical methods and instrumentation issues, implementing effective solutions. Contribute to the investigation of out-of-specification (OOS) results and deviations related to raw material testing. Ensure accurate and timely documentation of all laboratory activities and results in compliance with regulatory requirements. Stay updated on relevant pharmacopeial updates (e.g., USP, BP, EP) and regulatory guidelines. Collaborate with procurement and R&D departments on raw material specifications and supplier qualification.

Mentor and train junior analysts as needed.

Bachelor's or Master's degree in Pharmacy, Chemistry, Analytical Chemistry, or a related scientific discipline. Minimum of 5 years of experience in pharmaceutical Quality Control, with a strong focus on raw material testing. Proficiency in operating and maintaining analytical instruments such as HPLC, GC, dissolution testers, and spectrophotometers. Solid understanding of pharmacopeial monographs and general chapters. Experience with method development and validation is highly advantageous.

Knowledge of GMP and GLP principles. Excellent attention to detail, organizational skills, and problem-solving abilities. Strong written and verbal communication skills. Ability to work effectively both independently and as part of a team in a laboratory setting.

Our client provides a competitive salary package commensurate with experience and expertise. Benefits include comprehensive medical insurance, a retirement savings plan, and potential for performance-based bonuses. Opportunities for professional development, including training on new analytical techniques and attendance at relevant industry seminars, are available. Paid time off includes annual leave and sick leave. This hybrid role in Klerksdorp, North West , offers a balance between laboratory work and potential remote data review or project work, providing flexibility.

Join a company that is committed to scientific rigor and offers a stable career path in pharmaceutical quality control.