Vacancy for  Regulatory Affairs Associate at Teva Pharmaceutical

Vacancy for  Regulatory Affairs Associate at Teva Pharmaceutical

Regulatory Affairs Associate


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. Teva invited application for the post of Regulatory Affairs Associate suitable candidate can apply through online.

Post : Regulatory Affairs Associate I

Job Description
• Publish and dispatch major and complex routine/lifecycle management eCTD submission projects for EU, US and Canada.
• Exposure in handling initial submissions publishing and transmitting quality submissions to agency.
• Perform document level publishing activities, troubleshoot document issues and perform quality control checks for submission ready documents as per the agency guidance.
• Collaborate with scientific personnel for planning, preparation, publishing and quality control checks of submissions.
• Hands on expertise in EU and US submissions from pre-approval to post approval activities like initial, variations, PSUR etc.
• Participate in Global Regulatory Affairs project teams
• Maintain working knowledge of internal and external publishing standards.
• Knowledge of ICH and eCTD related specification/guidelines governing regulatory submissions (eCTD, NeeS, paper)
• Must be aware of Technical systems like Global Insight, ISI Toolbox, Adobe Acrobat, Lorenz Validator
• Sees opportunities for creative problem solving while staying within the parameters of good practice. Generates unique but workable and useful solutions to difficult problems.

Candidate Profile :
• B. Pharm/M. Pharm/ Master of Life Sciences/M Pharm
• Total years of experience required for the role:  3-6 years with Regulatory Publishing experience in EU and US market
• Command over spoken and written English
• Sensitivity to the cultural diversity of a global organization

Additional Information
Qualification : M.Pharm/B.Pharm/ MSC
Location :  Navi Mumbai
Industry Type : Pharma / Healthcare / Clinical research
Functional Area :  Regulatory Affairs
End Date : 30th November, 2020