✨ AI Summary
This role involves two key positions within Quality Control: Supervisor and Specialist. The Quality Control Supervisor will oversee sampling, testing, and release of materials, ensure adherence to specifications and GMP/GLP, review data, investigate deviations, and manage instrument calibration. They will also train and guide QC analysts. The Quality Control Specialist will perform physical and chemical analyses of materials, handle hands-on testing with instruments like HPLC and UV, and document results accurately according to pharmacopeias and GMP standards.
Requirements include a Bachelor's degree in Pharmacy or Science (Chemistry). The Supervisor needs proven experience in pharmaceutical QC testing, familiarity with lab instruments (HPLC, UV, IR, titration), and knowledge of GMP, GLP, and pharmacopeias. Strong documentation, leadership, and communication skills are essential. The Specialist requires 1-3 years of experience in a QC lab and proficiency with laboratory equipment.
Requirements
1. Quality Control SupervisorBachelor's degree in Pharmacy or Science (Chemistry)Proven experience in QC testing of raw and packaging materials in the pharmaceutical industryHands-on experience with HPLC, UV, IR, titration, and other lab instrumentsGood knowledge of GMP, GLP, and pharmacopeias (USP, BP, Ph. Eur.)Strong documentation, data review, and reporting skillsLeadership, attention to detail, and a problem-solving mindsetGood communication and teamwork skills2. Quality Control SpecialistBachelor’s degree in Pharmacy or Science (Chemistry).Experience (1 to 3 years) in a quality control laboratory.Proficient in operating modern laboratory equipment with strict adherence to safety and quality guidelines.
Description
1. Quality Control SupervisorSupervise sampling, testing, and release of raw and packaging materials.Ensure all analyses are performed according to approved specifications, pharmacopeial methods, and GMP/GLP requirements.Review analytical data, test reports, and Certificates of Analysis (COA).Investigate OOS/OOT results and deviations, and follow up on Corrective and Preventive Actions (CAPA).Monitor instrument calibration, maintenance, and laboratory safety.Train, guide, and evaluate QC analysts.2. Quality Control SpecialistPerform physical and chemical analyses of raw materials, packaging materials, or finished products.Handle hands-on testing using laboratory instruments (e.g., HPLC, UV, IR).Document analytical results accurately in compliance with pharmacopeias (USP/BP) and GMP standards.