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Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India

Skilled in medical device packaging and Visual inspection, with expertise in strategic planning, documentation, aligned with cGMP standards.

Identify and execute appropriate workup and purification technique to produce an intermediary / final compound of desired quality

The objective of the role is to perform chemical synthesis of molecules, the role involves process development, process validation and transfer to production units.

Responsible for discussion and planning strategies for product development, executing them and recording them in E-Lab notebook. Identify and proactively discuss potential challenges along with possible way forward.

OSD-coating, Compression, Packing, Granulation, Ointment-External Preparation (General & Sterile Manufacturing). Injectable (Aseptic, SIP, CIP, Batch Manufaturing, Bulk Manufacturing, Dry Powder), Oral Liquid

Granules India is a vertically integrated, high-growth pharmaceutical company with 38 years of proven performance and increasing performance and increasing presence across the world.

Preparation, review and submission of Dossiers, Good exposure on Life Cycle Management. Handling Post approval & Pre approval

Execution QA comprehensively reviews rendering quality, Metadata, Content Matrices accuracy with the email build, Subscriber segmentation, Journey configurations, and deployment accuracies. Calls out and communicates all inconsistencies to Campaign Managers and Deployment teams.