Regulatory Affairs Associate Job in Toronto for Teva Canada |

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Regulatory Affairs Associate

October 19 2020
Industries Pharmaceutical, Biotechnology
Categories Pharma, Biotech, Sciences, R&D, Scientific and Regulatory affairs
Toronto, ON
Company Info
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. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!
Job Description

The Publishing Associate I, Regulatory Submissions Management, is responsible for responsible for the publishing and dispatch of basic and complex lifecycle management eCTD submissions and ensuring technical validation. They have a working knowledge of internal/external publishing standards, electronic publishing/viewing software tools and document management systems. Independently performs document level publishing activities, troubleshoots document issues and performs quality control checks for submission ready documents.

The tasks and responsibilities include, but are not limited to:

  • Publish and dispatch major and complex routine/lifecycle management eCTD submission projects
  • Perform document level publishing activities, troubleshoot document issues and perform quality control checks for submission ready documents
  • Collaborate with scientific personnel for planning, preparation, publishing and quality control checks of submissions.
  • Participate in Global Regulatory Affairs project teams
  • Maintain working knowledge of internal and external publishing standards
  • Required: Bachelor’s Degree. Preferred: Bachelor’s Degree in Life Sciences or Information Technology
  • Ideally 1+ years in Regulatory Operations/Regulatory Affairs. Preferred: Experience as a publisher for regulatory applications
  • Experience with Liquent InSight suite, Microsoft Office suite, Adobe, Documentum, and eCTD technology and basic understanding of IT infrastructure is ideal
  • Understanding of the drug development process. Knowledge of generics and branded product development a plus
  • Working knowledge of industry legislation and best practices
  • Strong knowledge of regulations/guidelines governing regulatory submissions (eCTD, NeeS, paper)
Regulatory Affairs
Sub Function
Medical Regulatory Affairs
Reports To

Senior Manager, Regulatory Affairs

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