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Author and Initiator of Annual Product Reviews, Kfar Saba OSD Plant

Date: Nov 19, 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

  1. Oversees the implementation of Standard Operating Procedures relating to Annual Product Reviews in the Plant and compliance with the requirements of Good Manufacturing Practice (cGMP).
  2. Responsible for the collection of all required data for the Annual Product Reviews, according to the annual schedule and relevant approved procedure. Initiate the process of preparation and approval of the Annual Product Reviews by the relevant personnel in the plant.
  3. Edits and evaluates the required data for the Annual Product Reviews and accordingly prepares the reviews.
  4. Ensures that the approved Annual Product Reviews are handled and archived according to the relevant approved procedures. 
  5. Undergoes self-inspection audits relating to Annual Product Reviews, cooperates with the auditors and ensures that corrective actions are implemented and effective. 


Bachelor's degree in Life Sciences – advantage.
Experience in the pharmaceutical industry and knowledge of GMP procedures - advantage
Experience and proficiency in Microsoft Office applications (Word and most importantly Excel) – required.
Good communication skills, teamwork, and working with various interfaces.
Proficiency in computerized systems, searching, locating data. 
Excellent multitasking ability.
Ability to work under pressure.
Accuracy, independent control.
Excellent English (both reading and writing)




Sub Function

Quality Compliance

Reports To

Sr Mgr Quality Assurance, Doc Center

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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.