FR&D – OSD – Pharma

Experience: 3–4 Years
Qualification: B.Pharm / M.Pharm / Pharmaceutical Sciences
CTC: ₹4–8 LPA (Based on experience and interview performance)

Role Summary

Support oral solid dosage (OSD) formulation development, laboratory trials, technology transfer, and pharmaceutical R&D activities. The role involves executing formulation experiments, managing development materials and equipment, maintaining technical documentation, and ensuring compliance with SOPs and regulatory requirements.

Key Responsibilities

• Execute OSD formulation development activities using Hot Melt Extrusion, Wet Granulation, and Dry Granulation.
• Conduct laboratory experiments, document observations, and evaluate development results.
• Support technology transfer activities under the guidance of the reporting manager.
• Plan and arrange required materials, equipment, and laboratory facilities for development trials.
• Manage development material inventory and coordinate timely procurement.
• Maintain documentation including laboratory trials, SOPs, specifications, MFRs, and BMRs.
• Prepare development protocols, reports, and technical documentation.
• Ensure formulation development activities comply with SOPs and regulatory guidelines.
• Monitor laboratory equipment, calibration status, and equipment logbooks.
• Ensure proper storage and handling of APIs, excipients, and packaging materials.
• Discuss development outcomes with supervisors and support planning of subsequent trials.
• Coordinate with internal teams to meet product development timelines and documentation requirements.

Required Skills

• OSD Formulation Development
• Hot Melt Extrusion
• Wet & Dry Granulation
• Pharmaceutical R&D & Laboratory Experiments
• Technology Transfer
• MFR / BMR & Pharmaceutical Documentation
• SOP & Regulatory Compliance
• Laboratory Equipment & Material Management
• Strong Analytical & Problem-Solving Skills
• Attention to Detail & Ability to Manage Multiple Tasks