We are excited to share an amazing job opening for an Executive – Regulatory Affairs at Cadila Pharmaceuticals Limited in Dholka, near Ahmedabad! 📍 This is a fantastic opportunity for individuals passionate about regulatory affairs to take their career to the next level.
About the Role 📝
As an Executive – Regulatory Affairs, you will be responsible for EU Regulatory Lifecycle Management, eCTD dossier preparation, and regulatory review and compliance of technical documents and labelling.
Key Responsibilities 📊
EU Regulatory Lifecycle Management, including variations, renewals, site transfers, and post-approval changes
eCTD dossier preparation, review, and submission for EU/UK markets
Strong cross-functional coordination with R&D, QA, QC, and CMOS
Regulatory review and compliance of technical documents and labelling
Requirements 📚
3-5 years of experience in regulatory affairs or a related field
Strong knowledge of EU regulatory requirements and guidelines
Excellent communication and coordination skills
What We Offer 🌈
CTC up to 7 LPA
Opportunity to work in a dynamic and innovative environment
Gain hands-on experience in regulatory affairs
Develop your skills and knowledge in a leading pharmaceutical company
How to Apply 📧
If you’re passionate about regulatory affairs and have a keen eye for detail, we’d love to hear from you! Please WhatsApp your resume to +91 90545 97169.
About Cadila Pharmaceuticals Limited 🌐
Cadila Pharmaceuticals Limited is a leading pharmaceutical company committed to improving the lives of patients and consumers around the world.
Conclusion 🌟
Don’t miss out on this amazing opportunity to join our team! Apply now and take your career to the next level! 🌟
