Job Description

- Key Responsibilities:
? Support formulation development activities for regulated and semi-regulated markets, ensuring alignment with project timelines and quality standards
? Conduct pre-formulation, API-excipient compatibility studies, and stability testing to evaluate formulation feasibility
? Assist in scale-up and technology transfer from R&D to manufacturing, ensuring smooth transition and documentation
? Prepare comprehensive technical documents including development reports, batch records, protocols, and validation documents
? Collaborate with cross-functional departments such as QA, QC, Regulatory Affairs, and Production for project coordination and troubleshooting
? Participate in process optimization and continuous improvement initiatives within the Product Development Cell (PDC)
? Ensure strict adherence to cGMP, GLP, and regulatory guidelines throughout the product lifecycle
? Maintain proper documentation and support regulatory filings as required for domestic and international submissions

Skills Required