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Quality Control Technician - Salt Lake City, UT 84116


Teva Pharmaceuticals



This position is responsible for providing reliable and expedient results from the testing and analysis of incoming materials, intermediates, finished products, swab samples, and other samples to support the commercial and development activities at the site in compliance with all regulatory requirements, company policies and procedures.




All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other related duties or assignments.


  • Responsible for testing and analyzing incoming materials, intermediates, finished products, swab samples and other samples of a limited scope and complexity of activity.
  • Responsible for preparing, maintaining and reviewing thorough records, documentation on solutions, sample preparation and investigational/experimental samples.
  • Responsible for performing or assisting with minor revisions to documentation such as Standard Operating Procedures, Test Methods and Specifications.
  • Responsible for coordinating and sending materials for contract laboratory testing.
  • Responsible for assisting with verification of compendial methods.
  • Responsible for performing or assisting with activities associated with the stability program including sampling and limited statistical analyses under the direction of senior analysts or management.
  • Responsible for assisting with activities related to the sampling of incoming materials as needed.
  • In Microbiology – Responsible for performing microbiology testing using good ASEPTIC technique.
  • Responsible for completing all training requirements and maintaining 100% compliance with all assignments.
  • Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP’s), Standard Operating Procedures (SOP’s) and Batch Record instructions.
  • Responsible for performing additional related duties as assigned.




Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered.





  • Requires a Bachelor’s degree, preferably in Chemistry or Microbiology, or equivalent education/experience.
  • Requires a minimum two (2) years experience in a laboratory environment




Sub Function

Manufacturing Quality Control

Reports To

Group Leader Quality Control

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.



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