IntelUr Pharma is seeking a skilled International Regulatory Affairs Specialist to join our team in Bengaluru, India! If you have a strong background in regulatory affairs and a passion for global health, we invite you to join us! 🌐
About the Role 📝
As an International Regulatory Affairs Specialist, you’ll play a key role in managing regulatory submissions and ensuring compliance with global health authorities.
Responsibilities 📊
Compile and verify regulatory documents for CIS, MENA, and ASEAN regions
Prepare and submit regulatory documents to global health authorities
Collaborate with cross-functional teams to support international regulatory submissions
Ensure compliance with electronic submission standards (e.g., ACTD, eCTD, NeeS)
Requirements 📚
Postgraduate degree in Pharmacy/Life Sciences or a related field
3-4 years of Pharmaceutical Regulatory Affairs experience
Hands-on experience across ROW markets
Strong expertise in dossier compilation and authorisation
What We Offer 🌈
Competitive salary and benefits
Opportunities for growth and learning
Collaborative and dynamic work environment
Training and development programs
How to Apply 📧
Send your resume to contact@intelurpharma.com. Join IntelUr Pharma and be part of a dynamic team driving innovation in global health! 🚀
About IntelUr Pharma 🌟
IntelUr Pharma is a leading pharmaceutical company, committed to delivering high-quality products and services to improve global health.
Conclusion 🌟
Join IntelUr Pharma and take your career to the next level! Apply now and be part of a team making a difference in global health! 🌟
