Company Introduction
Noronic Pharmaceutical Private Limited is engaged in the development and manufacturing of regulated pharmaceutical formulations for domestic healthcare markets.
Core Responsibilities
- Prepare batch manufacturing records and batch packaging records using approved master documents.
- Review completed batch records against specification sheets and checklist formats.
- Compile validation files by arranging protocols reports and approval pages.
- Prepare stability study sample labels logs and controlled documentation files.
- Verify line clearance records area cleaning logs and equipment usage sheets.
- File reviewed quality documents into archival storage systems.
Skills and Technical Exposure
- Batch manufacturing records batch packaging records and validation documentation.
- Stability chambers temperature and humidity monitoring devices.
- Document control registers logbooks and quality checklists.
- Good Manufacturing Practice manuals and site quality procedures.
- Microsoft Word and spreadsheet tools for controlled documentation.
Experience Context
- Work is carried out within a pharmaceutical manufacturing facility and document review areas.
- Daily handling involves multiple production batches and packaging lots.
- Incomplete document review delays batch release and regulatory submissions.
- Quality documentation gaps directly affect compliance inspections.
How to Apply
hr@noronichpharma.com