Company Introduction
Radicon Laboratories Ltd operates pharmaceutical manufacturing facilities supplying regulated formulations to domestic and international markets.
Core Responsibilities
- Review quality manuals, SOP binders, and controlled documents against current regulatory requirements.
- Update master document lists and archive superseded records within the document control system.
- Track CAPA records using approved formats and maintain closure evidence files.
- Prepare internal audit schedules and compile completed audit reports.
- Verify training records and attach attendance sheets to qualification files.
- Support regulatory inspection readiness by arranging approved quality documentation.
Skills & Technical Exposure
- Quality manuals, SOPs, and controlled document registers.
- CAPA forms, deviation logs, and change control documents.
- Internal audit checklists and compliance trackers.
- Pharmaceutical quality management systems.
- Regulatory guideline documents.
Experience Context
- Work is carried out in a pharmaceutical manufacturing and quality office environment.
- Daily exposure includes multiple controlled documents and audit records.
- Without this role, documentation lapses delay audits and regulatory approvals.
How to Apply
garima_hr@radiconlab.com
