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Quality Analyst I - 6015

Date: Dec 24, 2018

Location: Parsippany, New Jersey, US, 07054

Company: Teva Pharmaceuticals

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!

Job Description

Position Summary

Responsible for insuring that all drug, biologic, combination or device products produced by Teva’s Third Party external manufacturing and packaging partners meets the established standards of quality including reliability, usability and performance.

Key Responsibilities

  • Insure ongoing compliance with quality and industry regulatory requirements for cGMPs, 21CFR 210/211, 21CFR 820 and 21CFR Part 4.
  • Responsible for release of product manufactured and/or packaged at Teva’s Third Party Suppliers located in the U.S.
  • Review Quality Customer Complaint investigations, non-conformance reports and Laboratory Investigations ensuring all necessary components are included.
  • Develop, recommend and monitor corrective and preventive actions (CAPA) and CAPA effectiveness reviews within the TrackWise system.
  • 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 management critical issues that may impact product on the market or product intended for the commercial market.
  • Review validation protocols and reports for activities occurring at Third Party Suppliers.
  • Represent the TPO Quality department and act as the primary contact for various cross functional teams involving product transfers, new product launches, supply chain activities, etc.



  • Bachelor’s degree in a related scientific discipline



  • Minimum of one (1) year experience in a Pharmaceutical FDA regulated industry in Quality Assurance or related field.
  • Must have working knowledge of cGMPs, CFR, ICH and applicable international regulations/guidelines.
  • Experience with Investigations, Change Controls, Product Release, CAPA, Validations, preferred. 
  • Experience with external pharmaceutical manufacturing, packaging, testing or devices is desired.
  • Strong computer skills including TrackWise, Oracle and SAP is desired.



Sub Function

Supplier Quality

Reports To

Quality Manager

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, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

Nearest Major Market: New York City
Nearest Secondary Market: Newark