Job Summary The QC Analyst is responsible for performing analytical testing of raw materials in-process samples and finished pharmaceutical products to ensure compliance with USFDA regulations cGMP standards and internal specifications This role is critical in maintaining product quality safety and efficacy Key Responsibilities Analytical Testing Conduct chemical physical and microbiological tests using techniques such as HPLC GC UV-Vis FTIR titration and dissolution Perform stability studies and method validation as per regulatory guidelines Documentation Compliance Maintain accurate and complete records of all testing activities in compliance with GDP Document and investigate any Out-of-Specification OOS results Ensure adherence to cGMP GLP and USFDA regulations Equipment Handling Calibrate maintain and troubleshoot laboratory instruments Ensure proper usage and upkeep of analytical equipment Cross-Functional Collaboration Coordinate with Production QA and R D teams to resolve quality issues Participate in internal and external audits Continuous Improvement Assist in developing and validating new analytical methods Recommend improvements to testing procedures and quality systems Qualifications Bachelor s or Master s degree in Chemistry Pharmaceutical Sciences or related field 2-5 years of experience in a pharmaceutical QC laboratory preferably in a USFDA-approved facility Hands-on experience with analytical instruments and techniques Knowledge of regulatory guidelines USFDA ICH WHO Solid attention to detail and analytical skills Preferred Certifications Certified Quality Analyst CQA Training in cGMP GLP and data integrity Soft Skills Excellent communication and documentation skills Ability to work independently and in a team Problem-solving and critical thinking abilities

📌 Senior Officer - Quality Control (Dadra)
🏢 Sun Pharmaceutical Industries
📍 Dadra