Quality Control Officer

As the Quality Control Operations Manager in a WHO-GMP & ISO approved Tablets and Capsule manufacturing facility, your role involves the following responsibilities: - Performing HPLC and Dissolution analysis. - Reviewing and checking all Raw material, packing material, bulk and finish product specification, method of analysis, and all worksheets. - Reviewing and checking Different validation protocols like process, cleaning, analytical method. - Reviewing and checking Stability study and hold time study protocols. - Ensuring timely sampling and analysis of incoming materials, such as raw materials and packing materials. - Ensuring timely analysis of bulk, finish product, stability sample, and validation sample. Qualifications and Requirements: - Experience in 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. In addition to the specific responsibilities and qualifications, the company offers a full-time, permanent job type with day shift schedule and a yearly bonus. A FDA certification in Chemical and Physio Chemical Testing is required for this position. The work location is in person.,