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QA Shop Floor Specialist (KFS OSD)

Date: Jun 27, 2022

Location: Kfar Saba, IL, 1111

Company: Teva Pharmaceuticals

Who are we?

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

  • Ensures compliance to cGMP regulations in manufacturing area including all documentation complying with the company’s Standard Operating Procedures (SOPs), governmental regulations and other requirements where applicable.
  • Executes Quality Walk Around for operations activities in order to assure manufacturing compliance with pharmaceutical requirements.
  • Reviews and releases executed batch records and packaging records supporting release of the batches.
  • Supports production activities by performing in –process monitoring related tasks (i.e. purified water sampling, statistical checks (AQLs), etc.)
  • Supports the Investigation by initiation deviations and participate in the event response team preliminary investigation.
  • Use of electronic Systems (TrackWise, LabWare, Glorya, MES, SAP etc.)
  • Maintains work areas and performs job functions in a safe and efficient manner in accordance to company policies and procedures, CGMPs, and SOPs.
  • Interacts effectively with employees, manager and cross-functional peers.
  • Performs additional duties as assigned.


  • Bachelor's degree in Chemistry/Biology/Life Science or any other relevant degree.
  • Alternatively, a High School Diploma completed by relevant and verified Training/Certification for the role can be accepted on an exceptional basis.
  • At least 5 years proven experience in pharmaceutical manufacturing areas, QA background – advantage.
  • Ability to work cross-functionally.
  • Experience with computerized systems, including Microsoft Office applications.
  • Languages: Hebrew, good command of English is preference.
  • Work in three shifts.



Sub Function

Manufacturing Quality Assurance

Reports To

Dir Quality Assurance, 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.