Share this Job

Regulatory Affairs Department Manager, Kfar Saba - OSD, Sterile and Biologics

Date: Jan 13, 2022

Location: Kfar Saba, IL, 1111

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

  • Manages the Regulatory Affairs field in Kfar Saba site (for relevant markets only) for post approvals as well as pre-approvals where applicable.
  • Manages submission applications for products relevant to the KF site (for relevant markets only).
  • Responsible for implementation of new and updated regulations pertaining to Regulatory Affairs (for relevant markets only).
  • Supports the plants & units with regards to Regulatory Affairs issues.
  • Ensures the implementation of Standard Operating Procedures relating to the Regulatory Affairs group's activities and compliance with the requirements of Good Manufacturing Practice (cGMP).
  • Ensures that deviations pertaining to the Regulatory Affairs group's activities are reported and investigated, and their effect on product is assessed and documented. Ensures that corrective and preventive actions are effective
  • Ensures the correct implementation of the change control procedure pertaining to Regulatory Affairs group's activities so as to assess and prevent unintended adverse consequences resulting from changes.
  • Coordinates activities and develop working process with other Regulatory Offices at Teva, contactors and customers as applicable.


  • Proven work experience in Regulatory Affairs field.
  • Experience in leading a team.
  • At least BSc in Science.
  • Proven experience in collaboration and multitasking.
  • Influencing capabilities.


Regulatory Affairs

Sub Function

Medical Regulatory Affairs

Reports To

Sr Dir, Site Quality Head, Kfar Saba, Quality Mgmt.

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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.