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