Quality Control Head

As the Quality Control Head at Celogen Pharma Pvt. Ltd., you will be responsible for directing all laboratory operations related to testing of raw materials, packaging materials, in-process materials, and finished pharmaceutical products. Your role will involve ensuring strict compliance with current Good Laboratory Practices (GLP) and all applicable national and international regulatory standards to provide high-quality, timely analytical support for manufacturing and product release. **Key Responsibilities:** - **Analytical Testing:** - Perform routine and non-routine analytical testing using various techniques such as HPLC, KF, Dissolution, Titration, and Physical testing. - Ensure testing is conducted in accordance with approved pharmacopoeial methods and in-house specifications. - Operate, calibrate, and maintain analytical instruments for optimal performance. - **Data Review & Documentation:** - Thoroughly review analytical data for accuracy and compliance with procedures. - Prepare Certificates of Analysis and ensure accurate documentation of testing activities. - Maintain detailed and organized laboratory records. - **Investigations & Deviations:** - Participate in investigations, identify root causes, and recommend corrective actions. - Document and investigate laboratory deviations, ensuring adherence to procedures. - Support the implementation and verification of corrective actions. - **Method Development & Validation Support:** - Assist in developing, transferring, and validating analytical methods as per regulatory guidelines. - Provide technical input for method optimization. - **Compliance & Audits:** - Ensure adherence to Good Manufacturing Practices (GMP) and regulatory guidelines. - Participate in internal and external audits, providing necessary documentation and technical support. - **Training & Mentorship:** - Train junior analysts on analytical techniques and laboratory procedures. - Serve as a technical resource for team members. - **Safety & Housekeeping:** - Comply with laboratory safety procedures and maintain a clean, organized working environment. - Manage laboratory waste in accordance with environmental regulations. - **Continuous Improvement:** - Identify process improvement opportunities within the QC laboratory. - Contribute to the revision and creation of Standard Operating Procedures (SOPs). In addition to the above responsibilities, you will work in a hormone formulation manufacturing division and collaborate with internal departments like Manufacturing, Quality Assurance, Regulatory Affairs, and Research & Development to resolve quality issues and support process improvements. If you are interested in applying for this full-time position, please submit your resume and cover letter to n.anjali@celogenpharma.com. ,