Qc Executive

Key Responsibilities Perform chemical and instrumental analysis e g HPLC UV of raw materials in-process and finished products Conduct and document stability testing as per ICH guidelines Support and execute Analytical Method Validation AMV protocols Ensure adherence to Good Laboratory Practices GLP and SOPs Maintain accurate records reports and logbooks Participate in OOS OOT investigations and quality improvement initiatives Qualifications B Sc M Sc in Chemistry Pharmaceutical Sciences or related field 2-4 years of experience in a regulated pharmaceutical QC lab Hands-on experience in HPLC GC UV and other analytical instruments Knowledge of stability guidelines and AMV practices Job Types Full-time Permanent Pay 11 843 50 - 30 000 00 per month Supplemental Pay Performance bonus Work Location In person