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
Robust 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
Robust 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