1+ months

Validation Engineer

Salt Lake City, UT 84111
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!


We offer competitive pay, shift differentials and benefits including: Medical, Dental, Vision and Prescription coverage all starting on the first day of employment. We also offer Disability and Life Insurance, Paid Time Off, 100% up to 6% match on the 401(k), Employee Stock Purchase Plan and Tuition Assistance.  This position is located at our facility in Research Park, near the University of Utah (575 Chipeta Way, 84108).

Job Description

 Essential Job Functions:

  • Carries out responsibilities in accordance with the organizations policies, procedures, and state, federal and local laws.
  • Reviews electrical, mechanical and software/computer specifications in manufacturer and blue print form, and identifies critical parameters.
  • Writes protocols that challenge the critical parameters related to installation, operation, and performance of the related facility, utilities, computer systems or equipment, and assures that protocols are approved through proper channels.
  • Writes and revises validation protocols.
  • Executes validation and qualification protocols per related SOPs and assures that acceptance criterion related to validation and qualification protocols are met.
  • Interacts with all effected personnel in the execution of protocols and gathering of test data. Assures that all test data is gathered and recorded in accordance with cGMP requirements.
  • Analyzes data to ascertain if it meets related protocol acceptance criteria.
  • Writes deviation reports as required upon failures to meet protocol acceptance criteria.
  • Complies with all GMP and safety requirements, SOPs and Company policies and procedures.
  • Writes final reports and assures that they are approved through proper channels.
  • Develops and communicates project timeline and status.
  • Performs related duties as assigned.


  • Bachelors degree in Engineering or a related field from an accredited college or university required.



  • Minimum 4 years of engineering validation experience, preferably in a pharmaceutical environment.
Sub Function
Equipment Maintenance Technical Specialty
Reports To

Principal Validation Engineer

Tevas 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.


Posted: 2019-12-03 Expires: 2020-03-15

Join us at the forefront of pharmaceutical research and production. With state-of-the-art facilities, highly skilled colleagues, and a high-powered organizational culture, Teva offers you countless possibilities to make a real difference in people's lives and add value to your career.

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Validation Engineer

Teva Pharmaceuticals
Salt Lake City, UT 84111

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