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15.0 - 20.0 years
0 Lacs
anand, gujarat
On-site
As the Head of R&D at Krishang Pharma Private Limited, you will play a crucial role in driving cutting-edge development for regulated markets. You will be responsible for leading end-to-end product development, scale-up, and technology transfer activities. Collaboration with cross-functional teams will be essential to ensure successful product launches, cost-effective processes, and regulatory readiness. Key Responsibilities: - Lead R&D strategy and execution for corticosteroids, hormones, and general APIs - Oversee route scouting, process development, optimization, and plant scale-up - Ensure adherence to GMP, ICH, and international regulatory standards - Coordinate with QA/QC, Regulatory A...
Posted 3 weeks ago
8.0 - 10.0 years
8 - 10 Lacs
Hosur, Tamil Nadu, India
On-site
We are seeking a highly experienced and meticulous Manager - Regulatory Affairs to oversee and execute all regulatory activities for drug substances and products. The ideal candidate will be responsible for the preparation, submission, and management of various regulatory documents, ensuring compliance with global regulatory agencies. This role requires strong coordination skills, attention to detail, and a proactive approach to addressing regulatory requirements and challenges. Responsibilities: Oversee the preparation and review of Drug Master Files (DMF) / Common Technical Documents (CTD) for various drug substances. Manage the preparation and submission of Technical Packages / Product Do...
Posted 3 months ago
8.0 - 10.0 years
8 - 10 Lacs
Bengaluru, Karnataka, India
On-site
We are seeking a highly experienced and meticulous Manager - Regulatory Affairs to oversee and execute all regulatory activities for drug substances and products. The ideal candidate will be responsible for the preparation, submission, and management of various regulatory documents, ensuring compliance with global regulatory agencies. This role requires strong coordination skills, attention to detail, and a proactive approach to addressing regulatory requirements and challenges. Responsibilities: Oversee the preparation and review of Drug Master Files (DMF) / Common Technical Documents (CTD) for various drug substances. Manage the preparation and submission of Technical Packages / Product Do...
Posted 3 months ago
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