About the Role
Our client, a reputable pharmaceutical manufacturer, is seeking a diligent and experienced Senior Pharmaceutical Quality Control Analyst to join their laboratory team in Soweto, Gauteng . This critical role involves performing a wide range of analytical tests on raw materials, in-process samples, and finished products to ensure they meet stringent quality and regulatory specifications. The ideal candidate will possess a strong foundation in analytical chemistry, hands‑on experience with various laboratory instruments, and a thorough understanding of GMP principles. This is an on‑site position, requiring full‑time commitment within our state‑of‑the‑art laboratory facilities in Soweto . Your meticulous work will be vital in safeguarding the quality and safety of our pharmaceutical products.
Key Responsibilities
- Perform various analytical tests on raw materials, intermediates, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis spectroscopy, FTIR, and wet chemistry.
- Analyze test results, compare them against established specifications, and document findings accurately.
- Investigate out-of-specification (OOS) results and identify root causes, recommending corrective actions.
- Calibrate, maintain, and troubleshoot laboratory equipment to ensure optimal performance and accuracy.
- Prepare analytical methods and validation protocols, and execute method validation studies.
- Maintain laboratory notebooks and records in compliance with GMP and regulatory requirements.
- Prepare certificates of analysis (CoAs) for released products.
- Participate in internal and external audits as required.
- Ensure compliance with all safety procedures and laboratory best practices.
- Contribute to continuous improvement initiatives within the Quality Control laboratory.
Requirements
- Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
- Minimum of 4 years of experience in pharmaceutical quality control, with significant hands‑on experience in analytical testing.
- Proficiency in using and maintaining analytical instruments, particularly HPLC and GC.
- Solid understanding of GMP principles, pharmaceutical testing guidelines (e.g., USP, BP), and regulatory requirements.
- Excellent analytical and problem‑solving skills, with a high degree of accuracy and attention to detail.
- Strong written and verbal communication skills for documentation and reporting.
- Ability to work effectively both independently and as part of a team.
- Experience with laboratory information management systems (LIMS) is a plus.
- Must be able to work full‑time on‑site in Soweto, Gauteng .
- Demonstrated commitment to quality and safety in a laboratory setting.
Benefits
- competitive salary
- comprehensive medical coverage
- retirement savings plan
- performance‑based bonuses
- opportunities for professional development
- We provide a supportive and collaborative laboratory environment.
Join our dedicated team in Soweto, Gauteng and contribute to ensuring the highest standards of pharmaceutical quality.