Primary Responsibilities:
Development of ophthalmic and/or semisolid formulations for regulated markets.
Perform literature searches, product assessments, and formulation optimization studies.
Execute clinical, engineering, scale-up, exhibit, and validation batches.
Prepare and review development and manufacturing documents including PDRs, MFCs, BMRs, scale-up protocols, and technology transfer documents.
Maintain laboratory notebooks, project files, and development records in compliance with SOPs and regulatory requirements.
Support technology transfer, scale-up, troubleshooting, and cross-functional project activities.
Ensure adherence to cGMP, data integrity, safety, and documentation practices.
Collaborate effectively with Analytical, Regulatory, QA, and Manufacturing teams.
Reporting Team
Reporting Designation: Senior Manager
Reporting Department: Formulation Development - US
Educational qualifications preferred
Category: Masters in Pharma
Field specialization: Pharmaceutics
Degree: MPharma
Required work experience
Industry: Pharmaceuticals
Role: Individual Contributor
Years of experience: 2 to 4 years
📌 Formulation Scientist R&d Ahmedabad (India)
🏢 Zydus Group
📍 India
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