Quality Control Officer

This position is responsible for managing all Quality Control Operations of a WHO-GMP & ISO approved Tablets and Capsule manufacturing facility. Specific Responsibilities: To perform HPLC and Dissolution analysis. To review and check all Raw material, packing material, bulk and finish product specification, method of analysis and all worksheet. To review and check Different validation protocol like process, cleaning, analytical method. To review and check Stability study and hold time study protocol. To ensure for timely sampling and analysis of incoming materials, like raw materials, packing materials. To ensure for timely analysis of bulk, finish product, stability sample and validation sample. Qualifications / Requirements: Experience of performing HPLC analysis. Bachelors degree in a scientific discipline (Masters Preferred). 3-7+ years of hands-on experience in the pharmaceutical industry, with specific experience in Quality Control. Job Types: Full-time, Permanent Schedule: Day shift Yearly bonus License/Certification: FDA certification Chemical and Physio Chemical Testing. (Required) Work Location: In person,