Teva Pharmaceuticals is seeking a highly motivated and experienced Regulatory Affairs Associate I to join their team in Navi Mumbai. As a Regulatory Affairs Associate I, you will play a critical role in managing regulatory affairs for the EU market.
📍Job Details:
Location: Navi Mumbai
Experience: 1-3 years of experience in RIMS/Veeva Vault/Article 57/XEVMPD for the EU market
Qualifications: Bachelor’s or Master’s degree in Life Sciences or Pharmacy
🧩Key Responsibilities:
Manage regulatory affairs for the EU market
Ensure compliance with EU regulatory requirements
Work with cross-functional teams to ensure regulatory submissions are accurate and timely
✅Requirements:
Q1-3 years of experience in RIMS/Veeva Vault/Article 57/XEVMPD for the EU market
Bachelor’s or Master’s degree in Life Sciences or Pharmacy
Strong knowledge of EU regulatory requirements and guidelines
Excellent communication and organisational skills
🌟What We Offer:
Opportunity to work with a leading pharmaceutical company
Career growth and development opportunities
Collaborative and dynamic work environment
📧 How to Apply
If you’re ready to make a difference in the global pharma landscape, send your updated CV to:
📩 Apeksha.Shinde01@teva.co.in
✅Why Work with Teva Pharmaceuticals:
Opportunity to work with a leading pharmaceutical company
Career growth and development opportunities
Collaborative and dynamic work environment
Competitive salary and benefits package
By working with Teva Pharmaceuticals, you will have the opportunity to develop your skills and expertise in regulatory affairs, while contributing to the success of our organisation. Apply now to join our team!