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.

- Valuable analytical, troubleshooting, and scientific writing skills.

📌 NDDS - OSD (Ahmedabad)
🏢 Intas
📍 Ahmedabad