Company Introduction
Privi Life Sciences Pvt. Ltd. develops and manufactures specialty chemical and life science products for regulated global markets.
Core Responsibilities
- Compile registration dossiers by assembling technical data, study reports, and statutory forms.
- Review raw data files and summaries before inclusion in regulatory submission folders.
- Prepare application checklists and track document completeness using submission trackers.
- Label, index, and archive regulatory files in physical cabinets and electronic repositories.
- Update amendment pages by replacing revised documents in approved submission sets.
- Print, bind, and paginate submission copies according to authority-specific formats.
Skills & Technical Exposure
- Regulatory submission dossiers and country-specific application formats.
- eCTD publishing tools and document management systems.
- Guideline documents issued by agricultural and chemical authorities.
- Technical summaries, study reports, and compliance checklists.
- Controlled document archives and version control logs.
Experience Context
- Work is carried out in corporate regulatory offices supporting manufacturing units.
- Assignments may cover multiple products and submissions prepared in parallel.
- Without this role, submission timelines, document traceability, and approval cycles stall.
How to Apply
alpana.deshmukh@privi.co.in
