About the Role
Our client, a respected pharmaceutical manufacturing company, is seeking a diligent Quality Control Analyst to join their laboratory team. This role is essential for ensuring the quality and safety of pharmaceutical products through rigorous analytical testing. You will perform a variety of chemical and physical tests on raw materials, in-process samples, and finished products to ensure they meet established specifications and regulatory standards. This position is located in Upington, Northern Cape , an area known for its growing industrial sector. The ideal candidate will have a strong background in analytical chemistry and experience working in a regulated laboratory environment. You will play a key role in upholding the company's commitment to delivering high-quality pharmaceuticals.
Key Responsibilities
- Perform routine and non-routine analytical testing on raw materials, intermediates, and finished products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, FTIR).
- Prepare reagents, solutions, and standards for analytical testing.
- Operate and maintain laboratory equipment, ensuring calibration and performance verification.
- Document all testing procedures and results accurately in laboratory notebooks and electronic systems.
- Analyze test data, interpret results, and report any deviations or out-of-specification (OOS) findings.
- Assist in the investigation of OOS results and deviations.
- Maintain a clean and organized laboratory environment, adhering to safety protocols.
- Participate in method validation and transfer activities as required.
- Ensure compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
- Contribute to continuous improvement initiatives within the QC laboratory.
Requirements
- Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific discipline.
- Minimum of 1-2 years of experience in a Quality Control laboratory, preferably within the pharmaceutical industry.
- Proficiency in analytical techniques such as HPLC, GC, and wet chemistry methods.
- Familiarity with pharmaceutical quality systems and regulatory requirements (e.g., GMP).
- Strong attention to detail and accuracy in performing tests and recording data.
- Good understanding of laboratory safety procedures.
- Ability to work independently and as part of a team in a fast-paced environment.
- Basic computer skills, including experience with LIMS and MS Office.
- Strong organizational and time management skills.
Benefits
- Our client offers a competitive salary, performance bonuses, and a comprehensive benefits package including medical aid, pension fund, and opportunities for professional development.
- The company promotes a culture of quality, safety, and teamwork.
- Join a dedicated laboratory team in Upington, Northern Cape , and contribute to ensuring the quality and safety of essential pharmaceutical products.