Natura Vitalis Industries Pvt Ltd.

Position: Pharma Quality Control Officer - FDA Schedule M Documentation Qualification: Min. B. Pharma degree (mandatory) Location: Gurgaon, Haryana Experience: Min. 3 years Salary: Open/Negotiable - based on qualification, experience, and candidates expectation. Candidates are requested to mention their expected salary in the application / resume. Key Responsibilities: Ensure compliance with Schedule M requirements as per FDA and company SOPs. Prepare, review, and update QC/QA and other records, logbooks, and test reports. Maintain and review proper documentation in accordance with FDA Schedule M regulatory standards . Conduct sampling, testing, and analysis of raw materials, in-process materials and finished products. Calibrate, operate, and maintain analytical instruments like - HPLC, GC-MS, UV etc. Monitor and ensure adherence to company quality standards across all departments. Coordinate with QA for deviations, OOS, and CAPA documentation. Assist in regulatory audits and internal quality audits. Ensure proper data integrity, record-keeping, and sample management. Desired Candidate Profile: B.Pharma degree (mandatory). Knowledge of Schedule M and FDA documentation requirements . Strong understanding of cGMP, GLP, and regulatory expectations. Good analytical skills and attention to detail. Proficient in documentation and compliance handling. Experience with pharma QC instruments preferred.