Senior Pharmaceutical Quality Control Analyst

Our client, a leading pharmaceutical innovator, is seeking a highly skilled and motivated Senior Pharmaceutical Quality Control Analyst to join their dynamic team in Midrand, Gauteng
. This is a critical role responsible for ensuring the highest standards of quality and compliance in our pharmaceutical products. You will be instrumental in upholding our commitment to safety and efficacy through rigorous testing and analysis. The successful candidate will leverage their extensive experience to contribute to process improvements and mentor junior team members. This position offers a unique opportunity to grow within a well-established organization that values scientific excellence and professional development.

We are looking for an individual with a keen eye for detail and a passion for pharmaceutical sciences, contributing to a healthier future through unwavering quality assurance. The work environment in Midrand, Gauteng is collaborative and forward-thinking, fostering innovation and dedication.

• Conduct comprehensive analytical testing of raw materials, in-process samples, and finished pharmaceutical products using advanced analytical techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Develop, validate, and transfer analytical methods in compliance with regulatory guidelines (e.g., ICH, FDA, SAHPRA).
• Interpret complex analytical data, troubleshoot method deviations, and prepare detailed investigation reports.
• Maintain laboratory equipment, ensuring calibration, qualification, and proper functioning.
• Ensure all laboratory activities comply with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Collaborate with R&D, production, and regulatory affairs departments to resolve quality issues and support product lifecycle management.
• Mentor and train junior analysts, providing guidance on testing procedures and compliance standards.
• Contribute to the continuous improvement of quality control processes and laboratory operations.
• Prepare and review analytical documentation, including test methods, validation reports, and certificates of analysis.
• Participate in internal and external audits, ensuring readiness and compliance.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biochemistry, or a related life science field.
• Minimum of 5 years of experience in pharmaceutical quality control, with a strong focus on analytical chemistry.
• Proven expertise in various analytical instrumentation and their applications (HPLC, GC, MS, spectroscopy).
• In-depth knowledge of regulatory requirements and guidelines (ICH, GMP, GLP) within the pharmaceutical industry.
• Experience in method development and validation.
• Excellent data interpretation and problem-solving skills.
• Strong written and verbal communication skills in English.
• Ability to work independently and as part of a team in a fast-paced environment.
• Detail-oriented with exceptional organizational skills.
• Previous experience in a supervisory or mentoring role is advantageous.

Our client offers a competitive remuneration package, comprehensive health insurance, generous paid time off, and opportunities for professional development and further education. Join a supportive work environment in Midrand, Gauteng where your contributions are valued, and career progression is encouraged. The company invests in its employees, providing access to cutting-edge technology and a culture of continuous learning. Furthermore, you will be part of a team that makes a tangible difference in public health.