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Sam Global Biocare Pvt. Ltd., a leading pharmaceutical company with a focus on international markets, is hiring a Drug Regulatory Affairs Specialist in Gurgaon (Sector 67, Haryana). This role is ideal for professionals with strong knowledge of global regulatory standards, including ICH and WHO guidelines, to support product approvals in the Middle East and African regions. If you have a B.Pharm or M.Pharm degree and are ready to take your regulatory career global, this opportunity is for you.
Key Responsibilities
- Prepare and submit comprehensive regulatory dossiers for international markets, including the Middle East and Africa.
- Ensure compliance with international regulatory frameworks such as ICH and WHO standards.
- Collaborate with cross-functional teams to facilitate smooth product approvals globally.
- Monitor evolving regulations in target markets to ensure ongoing compliance.
- Maintain accurate documentation and reporting to support regulatory submissions.
Qualifications & Skills
- Education: B.Pharm or M.Pharm with strong knowledge of global regulatory requirements (beyond CDSCO India).
- Proven understanding of international regulatory standards for pharmaceuticals.
- Excellent documentation, communication, and coordination skills.
- Detail-oriented, proactive, and capable of managing multiple regulatory submissions.
Benefits & Salary
- Competitive annual package: ₹3,00,000 – ₹3,60,000.
- Opportunity to gain international regulatory exposure.
- Work with a high-performing team and contribute to global pharmaceutical expansions.
How to Apply
Interested candidates can apply via:
- WhatsApp: +91 9289741168
- Email: deepak@samglobalbiocare.com
Ensure your CV highlights your experience with international regulatory submissions and compliance.
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