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Medopharm, a leading name in the pharmaceutical industry, is actively looking to expand its Regulatory Affairs team. With a strong focus on regulated markets and global compliance, Medopharm continues to provide high-quality, affordable medications to patients around the world. As part of our growth strategy, we are seeking experienced professionals who are ready to make a meaningful impact in the field of regulatory affairs.
Position: Regulatory Affairs Specialist
This role offers an exciting opportunity to be part of a dynamic, forward-thinking team that plays a critical role in ensuring regulatory compliance and supporting the company’s international product registrations.
Qualifications Required:
✔️ Over 5 Years of Pharma Experience
Candidates must have at least five years of experience in regulatory affairs within the pharmaceutical sector, specifically focusing on bioequivalence (BE) studies for regulated markets and WHO Prequalification (WHO PQ).
✔️ Experience in European Markets
Familiarity and hands-on experience working with European regulatory authorities is a key requirement, ensuring smooth registration and approval processes.
✔️ Dossier Preparation & Query Handling
Applicants must possess strong knowledge in dossier compilation and responding to regulatory queries efficiently and accurately.
Why Join Medopharm?
Medopharm offers a collaborative work environment, growth opportunities, and the chance to work on international regulatory projects that make a global difference. As part of our team, you’ll be at the forefront of ensuring safe and effective medications reach the markets where they are needed most.
Apply Now!
If you meet the above qualifications and are ready to take your career to the next level, send your resume to:
📧 hr@medopharm.com
Be a part of a company that values innovation, compliance, and quality — Medopharm is the place where your regulatory expertise can truly make an impact.
