Location– Chennai
Responsibilities in Job
- Assist with regulatory submissions such as IND, NDA, ANDA, and DMF in CTD/eCTD formats.
- Support the publishing and bookmarking of regulatory documents.
- Archive and review submissions and ensure they meet timelines.
- Maintain compliance with both customer SOPs and company policies.
Qualifications and Skills
- 0 – 1 Year
- Familiarity with US-FDA, EMA, and other global regulatory bodies.
- Strong attention to detail and organizational skills.
How To Apply
mailto: recruitment.chennai@navitaslifesciences.com With Proper Subject Line For Which Position You are Applying
