Are you a regulatory affairs professional with experience in drugs, medical devices, vaccines, injectables, or biosimilars? Genedrift is hiring a Senior Executive – Regulatory Affairs to strengthen its compliance and submission processes. This is your chance to join a forward-thinking company focused on innovation and excellence in life sciences.
Key Responsibilities
As a Senior Executive – Regulatory Affairs at Genedrift, you will:
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- Prepare, review, and submit regulatory dossiers for drugs, medical devices, vaccines, injectables, and biosimilars.
- Ensure compliance with local and international regulatory requirements.
- Liaise with regulatory authorities and internal stakeholders for approvals.
- Support the lifecycle management of products, including renewals and variations.
- Maintain up-to-date knowledge of regulatory guidelines and industry trends.
Qualifications & Experience
- Minimum 3 years of work experience in regulatory affairs.
- Hands-on experience with drugs, medical devices, vaccines, injectables, and biosimilars.
- Strong knowledge of regulatory guidelines, submission formats, and compliance processes.
- Excellent communication, documentation, and project management skills.
Benefits
- Competitive salary and performance-based incentives (INR 6–10 LPA).
- Professional growth in a dynamic, innovative environment.
- Exposure to global regulatory standards and submissions.
- Collaborative and supportive team culture.
How to Apply
Interested candidates can send their CV to:
📧 astha@genedrift.com or divya@genedrift.com
Ensure your application highlights your experience in regulatory affairs for drugs, medical devices, vaccines, injectables, or biosimilars.
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