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Sovvaka Global is hiring talented professionals for the role of Executive – Regulatory Affairs in Mumbai.
If you hold a B.Pharm or M.Sc degree and have 1–3 years of regulatory experience, this is an excellent opportunity to grow your career with a fast-growing pharmaceutical organization.
Key Responsibilities
- Prepare, review, and submit regulatory dossiers as per global and domestic guidelines.
- Ensure compliance with regulatory standards, documentation formats, and timelines.
- Coordinate with cross-functional teams for data collection and technical accuracy.
- Support regulatory submissions for new products, renewals, variations, and post-approval documentation.
- Maintain regulatory archives and ensure audit-ready documentation.
- Monitor updates in drug regulatory policies, guidelines, and market requirements.
Eligibility & Qualifications
- Qualification: B.Pharm or M.Sc (Pharmaceutical Sciences / Chemistry / related fields)
- Experience:
- Version 1: 1–3 Years
- Version 2: 2–3 Years
- Location: Mumbai
- Strong understanding of Regulatory Affairs, dossier preparation, and product compliance.
- Excellent communication and documentation skills.
Benefits of Working with Sovvaka Global
- Competitive salary based on experience
- Exposure to a wide range of regulatory submissions
- Opportunity to work with experienced regulatory professionals
- Skill enhancement in compliance, documentation, and regulatory strategy
- Growth potential in a rapidly expanding pharma company
How to Apply
Eligible candidates can send their updated CV to:
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