Company Introduction
CLAPS Industries Pvt Ltd is an Indian pharmaceutical manufacturing organization focused on delivering regulated healthcare products through structured systems and documented manufacturing practices.
Core Responsibilities
- Review batch manufacturing records and batch packing records using approved formats and controlled document registers.
- Verify standard operating procedures against master copies stored in the quality documentation control system.
- Check raw data entries in logbooks, formats, and annexures maintained at production and quality locations.
- Monitor Good Manufacturing Practice compliance through physical verification of records, labels, and controlled forms.
- Assess line clearance records, equipment usage logs, and cleaning checklists generated during manufacturing stages.
- Maintain archival files for completed quality documents as per defined retention schedules.
Skills and Technical Exposure
- Good Manufacturing Practice guidelines and controlled documentation systems.
- Batch manufacturing records, batch packing records, and master formula records.
- Standard operating procedures, formats, and annexure control logs.
- Quality manuals, site policies, and record retention registers.
- Pharmaceutical plant documentation storage and retrieval systems.
Experience Context
- Exposure to a pharmaceutical manufacturing plant environment handling multiple production batches.
- Work involvement with daily quality documentation generated across production and packing areas.
- Interaction with physical records where missing or incorrect entries can impact batch release status.
How to Apply
Send resume to hr@clapspharma.com or contact 917802814488
