Regulatory Affairs Associate

25 Sep, 2019

Jobs

Regulatory Affairs Associate

Teva Pharmaceuticals
Parsippany, NJ

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 Regulatory Affairs Associate (Publishing Associate, Regulatory Submissions Management) is responsible for the publishing and dispatch of basic lifecycle management submissions and troubleshooting document issues. The Publishing Associate I follows defined standards and 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

 

Qualifications

Experience Required: 0 – 2 years in Regulatory Operations/Regulatory Affairs

Required: Bachelor’s Degree

Preferred: Bachelor’s Degree in Life Sciences or Information Technology

Experience: Prefer previous experience in Regulatory Operations or Regulatory Affairs. Will consider applicants with Co-op or Internship experience.

Experience with Microsoft Office and Adobe Acrobat

Function

Regulatory Affairs

Sub Function

Medical Regulatory Affairs

Reports To

Director, North America Regulatory Submissions Management

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva’s global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva’s policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.

Learn more here

Job posted: 2019-09-25