Senior Quality Control Analyst

Our client, a rapidly expanding pharmaceutical company, is seeking an experienced Senior Quality Control Analyst to join their dedicated team in Rustenburg, North West . This critical role will ensure that all manufactured pharmaceutical products meet the highest standards of quality, safety, and efficacy. You will be responsible for performing a wide range of analytical tests, maintaining laboratory equipment, and contributing to the continuous improvement of quality control processes.

The ideal candidate will possess meticulous attention to detail, a strong understanding of analytical chemistry, and extensive experience within a GMP-regulated environment. This is a fantastic opportunity to contribute to a vital aspect of pharmaceutical production and play a key role in safeguarding public health within the Rustenburg area. You will work in a modern facility, employing advanced analytical technologies to ensure product integrity.

• Perform routine and non-routine analytical testing of raw materials, in-process samples, and finished products using various techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Develop, validate, and transfer analytical methods as required.
• Calibrate, maintain, and troubleshoot laboratory instrumentation to ensure optimal performance.
• Review and interpret analytical data, ensuring accuracy and compliance with specifications.
• Document all laboratory activities meticulously in accordance with GMP guidelines and company SOPs.
• Investigate out-of-specification (OOS) results and deviations, participating in root cause analysis.
• Prepare Certificates of Analysis (CoA) and other quality documentation.
• Contribute to internal and external audits as a subject matter expert for QC operations.
• Train and mentor junior QC analysts, providing guidance and support.
• Ensure the efficient operation and upkeep of the QC laboratory in Rustenburg.

• Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Biochemistry, or a related scientific discipline.
• Minimum of 5 years of hands-on experience in a pharmaceutical Quality Control laboratory.
• Proficiency in a wide array of analytical techniques, particularly HPLC and GC.
• Thorough understanding of GMP regulations and ICH guidelines.
• Experience with method validation and transfer is essential.
• Strong data analysis and interpretation skills.
• Excellent organizational skills and the ability to manage multiple tasks efficiently.
• Proficiency in laboratory information management systems (LIMS) and relevant software.
• Effective written and verbal communication skills.
• A proactive approach to problem-solving and a commitment to quality in Rustenburg.

• Our client offers a competitive salary commensurate with experience, a comprehensive benefits package including medical aid, provident fund, and life insurance.
• Opportunities for professional development and continuous learning are provided.
• You will join a supportive and collaborative team environment focused on excellence.
• The position offers a stable career path with potential for advancement within the organization.
• We believe in work-life balance and provide ample paid time off.
• Embrace a career that directly impacts patient well-being in Rustenburg.