Openings: 3
Job Description
Roles and Responsibilities:
- Prepare regulatory dossiers, reports, and documentation for submissions.
- Coordinate with QA, QC, and R&D teams for data compilation.
- Ensure timely submission of applications to regulatory authorities.
- Maintain records of submissions and follow-ups.
- Assist in compliance with regulatory guidelines (CDSCO, FDA, etc.).
Qualifications:
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, or related fields.
- Strong understanding of regulatory affairs and compliance.
- Excellent documentation and communication skills.
- Attention to detail and ability to work in a team.
How to Apply?
Interested candidates can send their updated CV to:
Email: m.sneha@transasia.co.in
