Responsibilities Conduct comprehensive eye exams to diagnose and treat various eye diseases and vision problems. Perform surgical procedures to correct vision issues and treat eye diseases, including but not limited to cataracts, glaucoma, and corneal diseases. Prescribe and fit eyeglasses and contact lenses. Provide pre-operative and post-operative care to patients undergoing eye surgeries. Collaborate with other medical professionals to provide holistic care to patients with systemic diseases affecting the eye. Stay updated with the latest developments in ophthalmology and incorporate advanced treatment methods. Participate in community outreach programs and educational workshops to promote eye health awareness.     Qualification & Experience MD or DO degree with a specialization in Ophthalmology. Valid medical license to practice in Assam. Proven experience as an Ophthalmologist, with a strong track record of successful diagnoses and surgeries. Excellent manual dexterity and hand-eye coordination for surgical procedures. Strong interpersonal and communication skills, with the ability to explain complex information to patients in a clear and compassionate manner. Commitment to continuing education and staying informed about the latest advancements in eye care.  

Responsibilities To facilitate harmonize and consistent implementation of Quality System and procedures at site alignment with Corporate Quality Policies/Procedures. To review documents pertaining to QMS & Compliance. Responsible for ensuring compliance of Quality Management System. To attend Site Training Program as per site training program and Global Quality Standards requirements. Dossier documents Submission after review against request received from Corporate regulatory affairs. Query response for submitted dossier against request received from Corporate regulatory affairs. Export dispatch related query response for approved art work of printed PM, Primary-packing material, overprinting and if other requirement is there. Export Harmonization activity between existing and new change implement for Product. Review and approval of change control and deviation through QMS software and prior approval activity from Regulatory if require as an impact analysis with require detail. Initiation of extension and variation proposal through QMS software Regulatory impact handling for Pharmacopoeia change like IP,BP,USP implementation for export market products. Location RA - Approval to Process Validation summary. Other departmental documents where signature require as location regulatory approval like  APR, etc. Product approval package review, approve and share approval detail to respective department. Any Additional activity allocated by the department head and site head.