Company Introduction
Eris Therapeutics develops and markets pharmaceutical formulations with a focus on regulated manufacturing standards and controlled quality systems.
Core Responsibilities
- Record in-process observations on batch manufacturing records while inspecting compression, coating, and packing stages.
- Check line clearance status using approved checklists, area labels, and material segregation boards on shop floors.
- Review filled IPQA formats, logbooks, and reconciliation sheets against issued master documents.
- Observe environmental conditions using temperature and humidity monitors placed inside production areas.
- Verify sample labeling, hold status tags, and container integrity during routine manufacturing runs.
- Document nonconforming observations on approved formats and attach photographic evidence where required.
Skills & Technical Exposure
- Batch manufacturing records and IPQA observation formats.
- Temperature and humidity monitoring devices.
- Weighing balances, label printers, and line clearance tools.
- Standard operating procedures and master formula documents.
- Deviation note sheets and investigation records.
Experience Context
- Daily presence within formulation plant blocks handling multiple batches per shift.
- Exposure to shop-floor areas where unchecked line status can halt batch release.
- Working alongside manufacturing equipment where missing documentation leads to regulatory queries.
How to Apply
recruitment@eristherapeutics.com
