Teva Pharmaceutical looking for Regulatory Affairs Associate | B.Pharm, M.Pharm, M.Sc apply

Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas.

Post : Regulatory Affairs Associate II

Job Description
• Lifecycle management on specific products for Europe and international markets
• Responsible at all times that regulatory modules under Product Manager responsibility are up to date, in accordance with agreed procedure as applicable
• Inform, prepare and submit variations either directly to authorities or to Teva’s 3rd party client business (Medis)
• Follow up on variation submissions, timelines and approvals, in accordance with agreed procedure as applicable
• Compile answers to any deficiency questions from authorities or clients
• Ensure outcomes of variations are communicated in timely manner and databases/lists are up to date at all times, in accordance with agreed procedure as applicable
• Regular status updates to management
• Goal setting and follow up together with his/her supervisor
• Provide regulatory guidance and support to other functions and Teva’s 3rd party client business (Medis)

Candidate Profile :
• M.Pharm/ MSc: 5+ years of experience in RA
• B.Pharm/BSc: 6+ years of experience in RA

Additional Information
Qualification : B.Pharm/M.Pharm, M.Sc, B.Sc
Location : Navi Mumbai
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : Regulatory Affairs
End Date : 30th September, 2021