Posted:3 days ago| Platform:
On-site
Full Time
About the Company Ajanta Pharma is a specialty pharmaceutical company providing quality medicines across 30+ countries in the world. We enjoy leadership in multiple molecules and therapeutic segments through 1st to Market products. About the Role Guiding a team of scientists to develop ophthalmic dosage forms for regulated markets on time. Responsibilities Implementation of stability studies as per ICH guidelines. Supervision and execution of manufacturing of Pre exhibit/ Exhibit batch which is manufactured at GMP locations. Guiding Documentation team for preparation of documents like status charts in excel, word documents, submission documents –MFR, PDR, ORML, OPML, TIPS, TFPS, MPR. Review and evaluation of submission documents MFR, PDR, ORML, OPML, TIPS, TFPS, MPR. Monitoring and execution of all activity related to ophthalmic development. Monitoring the implementation of SOP’s related to the department. Co-ordination with ADL, Purchase, QA, DRA, Marketing etc. for development and technology transfer activity for on time and smooth execution of batches. Guiding Laboratory assistants for cleaning of equipments as per cleaning SOPs, assembling/arranging the equipments for taking trial, overall cleanliness of area and equipment. Conduct In- House training of the ophthalmic department. Timely completion of all new development projects related to ophthalmic division. Any other job responsibility as assigned by reporting authority from time to time. Qualifications M. Pharm Required Skills Skills related to ophthalmic product development and team management. Preferred Skills Experience in regulated markets and familiarity with GMP locations. Equal Opportunity Statement We believe that diversity and inclusivity are essential to driving innovation, improving healthcare outcomes, and fostering a thriving workplace. We are committed to building a culture where individuals of all backgrounds, experiences, and identities feel respected, empowered, and valued. Show more Show less
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