About the Role
Our client, a renowned pharmaceutical entity, is actively seeking a meticulous and dedicated Pharmaceutical Quality Control Analyst to join their state-of-the-art facility in Vereeniging, Gauteng . This role is central to ensuring the highest standards of quality and safety for all manufactured pharmaceutical products. The analyst will perform a range of sophisticated tests and analyses on raw materials, in-process samples, and finished products using advanced laboratory instrumentation. This position offers a fantastic opportunity to contribute to a company committed to excellence and innovation in healthcare. The ideal candidate will possess a strong scientific background, a keen eye for detail, and a commitment to upholding stringent regulatory guidelines. You will be part of a team that directly impacts product integrity and patient well-being, working in a hybrid model that blends on-site laboratory work with flexible remote administrative tasks. This role is crucial for maintaining compliance and ensuring the efficacy of medications reaching the market.
Key Responsibilities
- Perform a variety of chemical, physical, and biological tests on raw materials, intermediates, and finished pharmaceutical products according to established specifications and standard operating procedures (SOPs).
- Operate and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers.
- Analyze test results, document findings accurately in laboratory notebooks and electronic systems, and report any deviations or out-of-specification (OOS) results.
- Ensure compliance with all relevant regulatory requirements, including GMP (Good Manufacturing Practices) and pharmacopeial standards.
- Participate in method validation and transfer activities for new analytical methods.
- Calibrate and maintain laboratory equipment, ensuring proper functioning and documentation.
- Prepare reagents, standards, and solutions required for testing.
- Assist in investigations of product quality complaints and deviations.
- Contribute to internal audits and inspections as required.
- Maintain a clean, organized, and safe laboratory environment.
Requirements
- Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or a related scientific discipline.
- Minimum of 3 years of experience in a pharmaceutical quality control laboratory setting.
- Proficiency in analytical techniques such as HPLC, GC, spectroscopy, and wet chemistry.
- Strong understanding of GMP, pharmacopeial methods (e.g., USP, EP), and regulatory expectations.
- Experience with laboratory information management systems (LIMS) is advantageous.
- Excellent documentation skills and attention to detail.
- Ability to troubleshoot analytical methods and instrumentation.
- Proficiency in data analysis and interpretation.
- Strong communication and interpersonal skills for effective collaboration.
- Ability to work effectively in a Vereeniging, Gauteng laboratory environment, with a portion of the work potentially being conducted remotely.
Benefits
- Competitive annual salary of R .
- Comprehensive medical aid and retirement fund contributions.
- Opportunities for professional development and advanced training.
- A dynamic and collaborative team environment.
- Access to modern laboratory facilities and advanced technologies.
- Paid leave and company holidays.
- Employee wellness programs.
- Potential for career advancement within the organization.
- Study leave for relevant certifications.
- Performance incentives.