Company Introduction
Marksans Pharma Ltd. develops and manufactures finished pharmaceutical formulations for regulated and emerging markets with a focus on quality-driven delivery.
Core Responsibilities
- Prepare technology transfer documents including MFR, BMR, and scale-up dossiers using approved templates.
- Review pilot batch records, exhibit batch records, and PDR documents prior to R&D handover.
- Observe granulation, compression, and coating trials on production equipment during transfer stages.
- Compare laboratory batch parameters with commercial batch parameters using batch comparison sheets.
- Record tooling specifications and machine settings during scale-up trials for reference packs.
- Document trial observations and batch outcomes in technology transfer reports for filing.
Skills & Technical Exposure
- Manufacturing documents such as MFR, BMR, PDR, and technology transfer protocols.
- Granulation equipment including rapid mixer granulators and fluid bed processors.
- Compression machines and coating pans used in solid oral dosage production.
- Exhibit batch and pilot batch preparation methods.
- Change control forms and development transfer checklists.
- R&D and manufacturing interface documentation.
Experience Context
- Work is based within pharmaceutical formulation plants and R&D scale-up areas.
- Daily exposure includes pilot batches, exhibit batches, and commercial-scale lots.
- Multiple products may undergo transfer simultaneously across shared equipment.
- Without this role, batch reproducibility and regulatory transfer readiness can fail.
How to Apply
muskan.shaikh@marksanspharma.com