Research Scientist - Tech Transfer

## Description

• Assist in the execution of **formulation and process technology transfers** from R&D to manufacturing sites (in-house and CMO).
• Conduct **scale-up and exhibit batches** under supervision, ensuring proper documentation and parameter tracking.
• Support in the **preparation and review of Batch Manufacturing Records (BMRs)** and **validation protocols/reports**.
• Coordinate with **R&D, QA, QC, Regulatory Affairs, and Manufacturing** teams for effective knowledge transfer and execution.
• Participate in **process investigations, troubleshooting, and deviation handling** during trial and validation batches.
• Assist in **equipment selection** and **capacity assessment** based on product-specific requirements.
• Ensure **document readiness for regulatory submissions**, respond to technical queries, and support audit preparation.
• Support **internal and external/vendor audits** by providing required documentation and technical inputs.
• Contribute to **continuous improvement** initiatives and support **knowledge-sharing activities** within the MSTG team.
• Prepare **data summaries, technical reports, and presentations** as per project or management requirements.
• Maintain **accurate records**, follow applicable **SOPs**, and ensure strict **GMP compliance** in all operations.

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## Qualifications
### **Qualifications & Skills**

• B.Pharm / M.Pharm in Pharmaceutics or Pharmaceutical Technology.
• 2–5 years of experience in formulation development, MS&T, or technology transfer.
• Exposure to **solid orals, liquids, or softgel capsule** dosage forms.
• Understanding of **scale-up principles**, **equipment functionality**, and **validation practices**.
• Familiar with **regulatory expectations** (USFDA, EU, etc.) and **cGMP** standards.
• Good communication, documentation, and teamwork skills.
• Willingness to travel to manufacturing sites as per project requirements.