1+ months

Regulatory Affairs Associate

Parsippany, NJ 07054
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!

 

We offer a competitive benefits package including Medical, Dental, Vision, and Prescription coverage starting on the first day. We also offer Disability and Life Insurance, Paid Time Off, 6% match on the 401(k), Employee Stock Purchase Plan and Tuition Assistance.For more information on Teva, check us out at www.tevapharm.com or www.tevausa.com

 

 

 

Responsible for the publishing and dispatch of basic lifecycle management submissions and troubleshooting document issues.  Works in close collaboration with senior staff and operational team members to ensure the creation of accurate, timely and technically competent regulatory submissions.

  • Build and dispatch lifecycle management submissions
  • Troubleshoot document issues with Adobe Acrobat & MS Word
  • Manage technical aspects for assigned submissions and status updates to concerned parties.
  • Collaborate with scientific personnel for planning, preparation, publishing and quality control checks of submissions.
  • Support submission efforts in other business units.
  • Maintain working knowledge of internal and external publishing standards
  • Identifies when data seems incorrect, incomplete or needs verification. Understands the business benefit and risk to steps being performed. Understands why steps are taken and can relate them to business objectives.
  • Sees existing problems/process inefficiencies and has novel approaches to solving those problems. Contributes original and resourceful ideas in brainstorming sessions.
     

Categories

Posted: 2020-04-23 Expires: 2020-06-08

Join us at the forefront of pharmaceutical research and production. With state-of-the-art facilities, highly skilled colleagues, and a high-powered organizational culture, Teva offers you countless possibilities to make a real difference in people's lives and add value to your career.

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Regulatory Affairs Associate

Teva Pharmaceuticals
Parsippany, NJ 07054

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