"Complete Success Guide for Pharma & Medical Students (2025-26)"
Pharma professionals with regulatory expertise have an excellent career opportunity! A leading global healthcare and technology company is inviting applications for the role of Executive – Regulatory Affairs in Bengaluru, India.
If you have 1–3 years of experience in India MDR and medical device regulations, this could be your next big step toward a successful regulatory career.
Location: Bengaluru, India
Experience Required: 1–3 years in Regulatory Affairs
Qualification: Degree in Regulatory Management or equivalent
As an Executive – Regulatory Affairs, you will be responsible for:
✔ Degree in Regulatory Management or equivalent
✔ 1–3 years of experience in Regulatory Affairs (India MDR focus)
✔ End-to-end MDR licensing experience
✔ Knowledge of regulatory license platforms
✔ Familiarity with legal metrology, labelling, UDI, MRP/Pricing, trade margins, and customs
✔ Advantageous: Knowledge of European MDR and FDA regulations
✔ Strong communication, compliance mindset, and stakeholder management
✅ Opportunity to work with a multinational healthcare & technology leader
✅ Exposure to international regulatory teams and global compliance processes
✅ Hands-on experience in MDR, PESO licensing, and GEM portal management
✅ Competitive salary package with growth opportunities in regulatory affairs
✅ Build a strong career in global healthcare compliance
Interested candidates can apply directly through the official career portal here:
👉 Apply for Executive – Regulatory Affairs (Bengaluru)
✨ This role is perfect for pharma professionals looking to grow in regulatory affairs and gain international exposure in a dynamic healthcare industry.
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