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Dir Quality Systems

Date: Sep 17, 2022

Location: Kfar Saba, IL, 111

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

  • Oversees the implementation of Standard Operating Procedures relating to equipment and critical systems, according to Good Manufacturing Practice (cGMP) requirements. 
  • Monitors and controls sampling plan of Water, CAS and Nitrogen systems.
  • Initiates and participates in risk assessment processes related to critical systems, equipment and information systems.
  • Participates in projects relating to equipment, critical systems and information technology .
  • Manages investigations of deviations related to equipment and critical systems, ensures that the deviations are reported, investigated and their effect on product is assessed and documented. Ensures that corrective and preventive actions are implemented and are effective.
  • Ensures the correct implementation of the change control procedure relating to equipment and critical systems as to assess and prevent unintended adverse consequences resulting from changes.

Qualifications

  • Bachelor’s Degree in Chemistry, Engineering, or related field
  •  8+ years of cGMP/Quality from manufacturing facilities 
  • Strong problem-solving skills 
  • Significant knowledge on QA Systems SOP development and risk assessment techniques   
  • Experience presenting QA systems topics during inspections
  • 5+ years of  managerial experience       
  • Proven ability to understand complex processes/problems  
  • Proven experience overseeing critical system,  equipment and IT systems 
     

Function

Quality

Sub Function

Quality Compliance

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.