Teva Pharma Regulatory Associate Job Vacancy – 2020
Teva invites postgraduate Pharma candidates for the post of R&D Intern. MPharma & B Pharma job opening at Teva. MSc & Pharma job opening 2020. Interested and eligible candidates may apply. Check out all the details on our website Rasayanika.com
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
Job Title: Regulatory Associate
Qualifications
B. Pharm/M. Pharm/ Master of Life Sciences – M Pharm preferred
Total years of experience required for the role: 1-3 years (preferred – Regulatory Publishing experience in EU and US market)
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
• 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
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