Strong understanding of pharmaceutical formulations and patent law basics. Proficiency in patent databases and search strategies.
Analytical mindset with excellent attention to detail. Good communication and technical writing skills.
Ability to manage shift plans for formulation activities. Operate and maintain equipment such as autoclaves and blending vessels CIP and SIP skids. Ability to manage shift plans for filling activities. Operate and maintain equipment such as a Vial Washer, Tunnel Sterilizer, filling and Capping Machine.
Perform real-time monitoring of production processes to ensure adherence to quality standards. Conduct routine inspections and in-process checks to verify compliance with specifications and protocols.
Review qualification protocols, reports, and documentation for accuracy, completeness, and compliance. Collaborate with cross-functional teams, including Quality Assurance, and Engineering, to ensure alignment and consistency in qualification practices.
Set and agree written goals and objectives, perform annual appraisal interviews and end of probation appraisals; submit promotion requests to management as appropriate. Ensure resource and recruitment are well aligned and timely managed in collaboration with relevant parties, participate in interviews for potential new hires.
Analytical Method Development, Validation, Transfer activities of test like Assay, RS, Dissolution and Solvent. Calibration of the Analytical instruments like HPLC, GCHS, IR, UV & Disso as per the master calibration schedule.