Role & responsibilities

- Develop MR, SR, CR, DR, pellet and multiarticulate formulations.
- Perform QbD based development and DOE studies.
- Execute scale up, exhibit, validation and commercial batches.
- Support technology transfer activities.
- Prepare development reports, protocols and regulatory documents.
- Coordinate with QA, QC, Production and Regulatory Affairs teams.

Required Skills

- Strong knowledge of NDDS and OSD formulation development.
- Experience in QbD, DOE and statistical evaluation.
- Knowledge of ICH guidelines and cGMP requirements.
- Scientific writing and troubleshooting skills.

Preferred Exposure

- Modified Release Technologies
- Multiarticulate and Palletization
- Hot Melt Extrusion
- Gastro Retentive Systems
- ANDA and Regulatory Filing Support

Preferred candidate profile

- Strong knowledge of NDDS technologies and OSD formulation development.
- Hands-on experience in QbD, DOE, and statistical tools.
- Understanding of cGMP, ICH Guidelines, and regulatory requirements.
- Expertise in tablet, capsule, pellet, and multiarticulate formulations.
- Positive analytical, troubleshooting, and scientific writing skills.

📌 NDDS - OSD (Ahmedabad)
🏢 Intas
📍 Ahmedabad