Company Introduction
Apitoria is a pharmaceutical manufacturer focused on active pharmaceutical ingredient development and large scale supply for regulated and semi regulated markets.
Core Responsibilities
- Oversee batch manufacturing at the active pharmaceutical ingredient plant using reactors, centrifuges, dryers, and distillation columns.
- Plan production schedules through master batch records, capacity loading sheets, and equipment utilization logs.
- Supervise technology transfer runs using scale up protocols, validation reports, and engineering change notes.
- Monitor plant performance through daily production registers, yield statements, and downtime analysis sheets.
- Review audit readiness using inspection checklists, corrective action reports, and compliance trackers.
- Control material flow by verifying bill of materials, inventory registers, and batch issue vouchers.
Skills and Technical Exposure
- Glass lined reactors, agitated vessels, centrifuges, vacuum tray dryers, and scrubber systems.
- Batch manufacturing records, master formula sheets, and production logbooks.
- Distributed control systems, programmable logic controllers, and manufacturing execution systems.
- Validation protocols, scale up reports, and technology transfer documentation.
- Regulatory inspection checklists, audit response files, and compliance dashboards.
Experience Context
- Work environment includes a pharmaceutical manufacturing plant handling multi step active pharmaceutical ingredient synthesis.
- Production scale covers multiple batches per campaign with high volume reactors and continuous utilities support.
- Without this role, batch timelines slip, capacity utilization drops, and regulatory commitments face risk.
How to Apply
sudha.hr@apitoria.com
