Company Introduction
Privi Life Sciences Pvt Ltd is a specialty chemical manufacturer supplying agrochemical and life science ingredients to regulated global markets.
Core Responsibilities
- Prepare international regulatory dossiers using registration templates, product specifications, and country specific submission formats.
- Compile technical documents such as safety data sheets, labels, and composition statements for overseas authorities.
- Submit registration files through regulatory portals and track acknowledgement receipts and query letters.
- Maintain registration trackers using spreadsheets, approval letters, and validity certificates.
- Review formulation data against regulatory guidelines and approved master documents.
- Archive regulatory correspondence, licenses, and approvals in controlled document repositories.
Skills and Technical Exposure
- International registration dossiers for agrochemical and specialty nutrient products.
- Safety data sheets, technical data sheets, and label artwork files.
- Regulatory submission portals and electronic document formats.
- Registration trackers, approval letters, and license documents.
- Guideline documents issued by global regulatory authorities.
Experience Context
- Work is performed in a corporate regulatory office supporting manufacturing plants and export supply chains.
- Handling of multiple country registrations and product variants occurs simultaneously.
- Without this role, product shipments face clearance delays and market access blocks.
How to Apply
Email alpana.deshmukh@privi.co.in
