4-5

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.

M.Pharm, B.Pharm, M.Sc, B.Sc Openings, OSD (Granulation, Compression, Coating, Capsule), Injectable (Dry Powder Injectable) 

Responsible for In-process production related activities in DP manufacturing, filling, and packing sections. Preparation of batch manufacturing records, process validation protocol/report of DP area and its associated records.

Routine microbiological testing and environmental monitoring to ensure compliance with regulatory standards and GMP guidelines.