Company Introduction
Medreich R&D, part of the Meiji Group, focuses on pharmaceutical formulation research, development, and lifecycle management for global markets.
Core Responsibilities
- Compile technology transfer packages including MFR, BMR, and scale-up reports for solid oral formulations.
- Review pilot batch data, exhibit batch records, and development summaries prior to manufacturing handover.
- Observe granulation, blending, compression, and coating runs on commercial equipment during transfer stages.
- Compare laboratory formulation parameters with commercial batch parameters using approved comparison sheets.
- Document tooling details, machine settings, and batch observations within transfer dossiers.
- Prepare transfer summary reports supporting regulatory and manufacturing readiness.
Skills & Technical Exposure
- Technology transfer documents including MFR, BMR, PDR, and scale-up reports.
- Solid oral manufacturing equipment such as granulators, blenders, tablet presses, and coating pans.
- Exhibit batch and pilot batch preparation methods.
- Change control documentation and development transfer checklists.
- Data comparison sheets and formulation development summaries.
- Regulatory filing support documentation.
Experience Context
- Work is performed within pharmaceutical R&D centers and commercial manufacturing plants.
- Assignments involve multiple solid oral products transitioning from development to scale.
- Batch sizes range from pilot scale to full commercial lots using shared equipment.
- Without this role, product transfers may stall, delaying commercialization and regulatory submissions.
How to Apply
vineeta.k@medreich.com