1+ months

Manager, QC Systems

Irvine, CA 92606

Company Info

If youre like people at Teva, you dare to be different. Were making well-being a way of life for our customers and our colleagues. Join us in helping to make healthcare more accessible to more patients, while supporting one of the most innovative teams in the industry.

Tevas Irvine, CA production site is one of our complex manufacturing and supply chain operations.

We are strengthening and adding to our critical teams with great talent and capabilities. Teva, a global organization, with a brand of evolving success.  Be part of it!


We offer a competitive benefits package including Medical, Dental, Vision and Prescription coverage starting on the first day. We also offer Disability and Life Insurance, Paid Time Off, 6% match on the 401(k), Employee Stock Purchase Plan and Tuition Assistance


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

Teva is searching for a Manager, QC Systems to join our team in Irvine!

This role will manage the laboratory instrumentation program including laboratory computer systems. This includes vendor management, performing calibrations, maintenance, troubleshooting and repair of instruments utilizing approved Methods, Procedures (SOPs) and Corporate policies while maintaining adherence to current industry standards (cGMPs, GLPs, etc.).  The role includes management of the full instrument lifecycle, from the drafting of capital requests through qualification activities and retirement of instruments. 


You will:

  • Partner with IT and other departments to maintain current computer systems and develop/offer solutions problems using existing Teva systems.
  • Research, propose and implement where new solutions are needed.
  • Maintain instrument files and manage instrument budget.
  • Mentor, educate and transfer knowledge to laboratory team.


  • BS in Chemistry or other related science required.
  • Minimum of 8 years of experience using and/or servicing laboratory instruments required.
  • Strong background in equipment maintenance and calibrations within pharmaceutical industry required.
  • Minimum 10 years of experience within a GLP/GMP Environment; Good understanding of Instrumentation and the maintenance thereof required.
  • Strong understanding of 21 CFR Part 11 and experience participating as a SME in regulatory inspections.
  • Proficiency with authoring and executing protocols and reports related to instrument PMs and new instrument IQ/OQ/PQ. 
  • The ability to troubleshoot laboratory instrumentation including: HPLC, GC, GC/MS, IC, IR, UV, Dissolution, Balances and Titrators. 
  • Practical knowledge of Empower 3, LabWare LIMS, ChemStation, Chromeleon, TrackWise, HPALM. 
  • Ability to investigate and implement appropriate corrective actions for instrumentation failures. Strong knowledge of instrument and computer qualification requirements.
  • Ability to train and transfer knowledge of instruments to laboratory team. Ability to manage instrument vendors and direct reports.
  • Ability to communicate effectively with excellent written and oral communication skills.
  • Ability to interact positively and collaborate with co-workers, management, internal stakeholders and vendors.



Sub Function

Manufacturing 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.

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.

We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. 


Posted: 2021-04-01 Expires: 2021-06-04

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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Manager, QC Systems

Teva Pharmaceuticals
Irvine, CA 92606

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