BDR Pharmaceuticals, one of India’s fastest-growing pharmaceutical companies, is expanding its Regulatory Affairs team. If you have experience in ROW regulatory submissions and want to take your career to the next level, this is an excellent opportunity to join a company known for innovation and global presence.
This role is based at Vadodara, Gujarat, and is ideal for professionals with 3–5 years of experience in Regulatory Affairs.
Key Responsibilities
As a Regulatory Affairs Officer/Sr. Officer (ROW), you will:
- Prepare, review, and compile regulatory documents in compliance with ROW guidelines.
- Support the maintenance and updating of product dossiers and regulatory files.
- Coordinate with formulation, QA, QC, and supply chain teams for required documentation.
- Monitor and interpret regulatory changes in ROW markets.
- Maintain records, databases, and documentation as per compliance.
- Provide regulatory support and guidance to ensure smooth project execution.
- Assist communication with international regulatory agencies (via the RA team).
Required Qualifications
To be successful in this role, you should have:
- B.Pharm / M.Pharm / Life Sciences degree or equivalent.
- 3–5 years of experience in Regulatory Affairs (ROW markets).
- Strong knowledge of international regulatory compliance.
- Good skills in regulatory documentation and dossier preparation.
- Excellent communication, organizational, and coordination abilities.
- Attention to detail with the ability to manage multiple projects.
Why Join BDR Pharmaceuticals?
- Work with one of India’s most dynamic pharma companies with a global footprint.
- Exposure to international regulatory frameworks across diverse markets.
- Supportive and collaborative work environment.
- Strong career growth opportunities in Regulatory Affairs.
- Competitive salary package (up to ₹6 LPA).
Application Process
Interested candidates can apply by sending their resume to:
📍 Job Location: Vadodara, Gujarat (On-site)
