Company Introduction
Innoxel Lifesciences is a pharmaceutical manufacturing organization focused on regulated injectable formulations for domestic and international markets.
Core Responsibilities
- Review validation protocols and reports using approved master documents and regulatory formats.
- Check batch manufacturing records against approved templates and archival logs.
- Examine vendor qualification files through audit checklists and assessment reports.
- Inspect in process quality assurance records at injectable manufacturing lines using control forms.
- Verify compliance records against United States Food and Drug Administration guidelines and internal standards.
- Maintain document cell files through indexing registers and controlled distribution records.
Skills and Technical Exposure
- Validation master plans and protocol documentation.
- Quality management system manuals and controlled formats.
- Vendor audit reports and qualification dossiers.
- In process quality assurance check sheets.
- Regulatory compliance records for injectable facilities.
Experience Context
- Work takes place inside an injectable manufacturing plant regulated by United States Food and Drug Administration standards.
- The role covers multiple production batches with extensive documentation review and line level checks.
- Without this role, batch release documentation and regulatory readiness collapse during inspections.
How to Apply
Email resume to vishal.joshi@innoxells.com
