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:

📩 hr@sovvakaglobal.com