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RA Team Leader

Date: Nov 18, 2020

Location: Kfar Saba, IL, 11111

Company: Teva Pharmaceuticals

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

Manage and lead RA team.

Key Responsibilities / Deliverables:

  • Manage and lead RA team in preparing submissions for US, EU and CA markets and responding to deficiency letters
  • Review submission files and deficiency letter responses
  • Provide regulatory guidance, support and resolve issues raised during product development and review period
  • Ensure team’s regulatory activities are carried out and tracked on a timely manner
  • Support pre-launch activities
  • Master’s degree in the field of science (e.g., chemistry/chemistry engineering, biothechnology/biotechnology engineering, pharmacology)
  • 3 year experience in Regulatory Affairs in a pharmaceutical company

Skills & Knowledge

  • Familiarity with drug development process, as related to manufacturing, quality control and research.
  • Strong management and leadership skills
  • Strong interpersonal/communication skills
  • Ability to manage time priorities and meet deadlines
  • Multitasking
  • Fluent in English (written and spoken)
  • Flexible/Ability to adapt to changes
  • Well-organized
  • Attention to details
  • Initiative
  • Self-motivated
Regulatory Affairs
Sub Function
Medical Regulatory Affairs
Reports To

Dir, GxR&D CMC Regulatory Affairs - KFS, Non-Steriles Gx RA

Already Working @TEVA?

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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.