3 Senior Analytical Chemist Pharmaceutical Quality Control jobs in Placements24

• Develop, validate, and transfer analytical methods for raw materials, in-process samples, and finished pharmaceutical products.
• Perform routine and non-routine analyses using techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
• Analyze and interpret analytical data, identify deviations, and investigate out-of-specification (OOS) results.
• Ensure all analytical activities comply with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
• Maintain laboratory equipment, perform calibrations, and ensure proper functioning of analytical instruments.
• Prepare and review analytical reports, method validation protocols, and stability study reports.
• Troubleshoot analytical methods and instrumentation issues.
• Train and mentor junior analytical chemists and technicians.
• Collaborate with formulation development, manufacturing, and regulatory affairs teams.
• Stay current with advancements in analytical chemistry and pharmaceutical quality control.

• M.Sc. or Ph.D. in Analytical Chemistry, Pharmaceutical Chemistry, or a related scientific discipline.
• Minimum of 5-7 years of relevant experience in analytical chemistry, specifically within the pharmaceutical industry.
• Proficiency with analytical instrumentation such as HPLC, GC, Mass Spectrometry (MS), UV-Vis, and dissolution apparatus.
• Strong understanding of pharmaceutical quality control principles and GMP regulations.
• Experience in method development, validation, and transfer.
• Excellent data interpretation and problem-solving skills.
• Strong written and verbal communication skills.
• Ability to manage multiple priorities and work effectively under pressure.
• Attention to detail and commitment to maintaining high-quality standards.
• Must be legally eligible to work in **Nigeria**.

Our client, a reputable pharmaceutical manufacturer, is seeking a highly skilled Senior Analytical Chemist to join their Quality Control department. This role is crucial for ensuring the quality and safety of our pharmaceutical products and is based in our modern facility in Kaduna, Kaduna, NG . The ideal candidate will have extensive experience with various analytical techniques, including HPLC, GC, spectroscopy (UV-Vis, IR), and dissolution testing. You will be responsible for developing, validating, and executing analytical methods for raw materials, in-process samples, and finished products. This position requires a meticulous approach, strong problem-solving skills, and a thorough understanding of regulatory guidelines (e.g., GMP). You will work collaboratively with the R&D, manufacturing, and quality assurance teams to maintain the highest standards of product quality. This is an excellent opportunity to contribute to the pharmaceutical industry and grow within a well-established organization. You will play a vital role in ensuring compliance and product integrity.

• Develop, validate, and transfer analytical methods for pharmaceutical products and raw materials.
• Perform routine quality control testing using techniques such as HPLC, GC, UV-Vis, IR, KF titration, and dissolution testing.
• Analyze samples from different stages of the manufacturing process to ensure compliance with specifications.
• Investigate out-of-specification (OOS) results and deviations, implementing corrective and preventive actions (CAPAs).
• Calibrate and maintain analytical instruments, ensuring their optimal performance.
• Prepare comprehensive analytical reports, method validation summaries, and stability study protocols.
• Ensure all analytical activities comply with Good Manufacturing Practices (GMP) and relevant regulatory guidelines.
• Troubleshoot analytical instrumentation and methodologies.
• Train and mentor junior analytical chemists.
• Contribute to process improvement initiatives within the Quality Control department.

• M.Sc. or Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or a related discipline.
• Minimum of 5 years of experience in analytical chemistry within the pharmaceutical industry, specifically in Quality Control.
• Strong hands-on experience with HPLC, GC, UV-Vis, IR spectroscopy, and dissolution apparatus.
• In-depth knowledge of method development and validation principles according to ICH guidelines.
• Familiarity with pharmacopeial methods (e.g., USP, EP).
• Understanding of GMP regulations and quality management systems.
• Excellent analytical, problem-solving, and critical thinking skills.
• Strong written and verbal communication skills.
• Ability to manage multiple tasks and prioritize effectively.
• Experience with LIMS is a plus.

Our client offers a competitive salary, comprehensive health and wellness benefits, performance incentives, and opportunities for professional development and continuing education. Employees benefit from working in a state-of-the-art facility with a strong emphasis on quality and innovation in Kaduna, Kaduna, NG . This role provides a stable career path within the pharmaceutical quality sector.