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Teva Pharmaceuticals Quality Analyst II in Parsippany, New Jersey

Quality Analyst II

Date: Mar 15, 2023


Parsippany, New Jersey, United States, 07054

Company: Teva Pharmaceuticals

Job Id: 44881

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


Responsible for ensuring all drug, biologic, and combination products produced by Teva’s Third Party external manufacturing and packaging partners meets the established standards of quality.


  • Assure ongoing compliance with quality and industry regulatory requirements for cGMPs, 21CFR 210/211, 21CFR 600/610, 21CFR 820 and 21CFR Part 4.

  • Collaborate with suppliers to assure the quality of their products, materials, components and/or operations.

  • Responsible for release of product manufactured and/or packaged at Teva’s Third Party Suppliers located in the U.S.

  • Provide Quality oversight for all manufacturing/packaging/testing at Teva’s Third Party Suppliers.

  • Receive, review Quality Customer Complaint investigations, non-conformance reports and Laboratory Investigations ensuring all necessary components are included.

  • Evaluate Third Party Supplier Annual product Reviews (APRs) against internal SOPs to identify trends and ensure a continued high level of quality.

  • Review, evaluate and approve change controls from Third Party Suppliers and act as the point of contact for all comments between internal departments and the site.

  • Communicate to senior level management critical issues that may impact product on the market or product intended for the commercial market.



  • Bachelor’s degree in a related scientific or technical discipline

  • Certifications such as Quality Auditor, Quality Engineer, Quality Improvement Associate and/or Six Sigma are a plus.


  • Minimum of 3 years’ experience in a Pharmaceutical FDA regulated industry in Quality Assurance or related field.

  • Must have in-depth knowledge of cGMPs, CFR, ICH and applicable international regulations/guidelines.

  • Experience with Investigations, Change Controls, Product Release, CAPA (preferred).

  • Experience with external pharmaceutical manufacturing, packaging, and testing (desired).

  • Works independently with minimal guidance

  • Strong computer skills including TrackWise, Excel, and SAP (desired).


  • Quality: attention to detail and accuracy, committed to excellence, suggests improvements to existing process, identifies root causes, owns and acts on quality issues.

  • Integrity/Ethics: Deals with others in a straightforward and honest manner, is accountable for own actions, maintains confidentiality, and supports company values.

  • Teamwork: meets all team deadlines and responsibilities, listens and values other’s opinions and acts as a resource for colleagues with less experience

  • Customer Focus: represents Teva in a professional and positive manner. Sets expectations of quality, solicits opinions and ideas and responds to customer quality inquiries.

  • Adaptability/flexibility: adjusts plans to meet changing needs, open to new ideas, takes on new responsibilities.

  • Able to:

  • Communicate well both verbally and written

  • Collect, manage and analyze data

  • Analyze and solve problems using existing solutions

  • Plan, prioritize and organize with minimal management oversight



Sub Function

Supplier Quality

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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

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