Teva Pharmaceuticals Quality Analyst III in Parsippany, New Jersey
Quality Analyst III
Date: Jul 21, 2021
Location: Parsippany, New Jersey, US, 07054
Company: Teva Pharmaceuticals
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 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. For more information on Teva, check us out at www.tevapharm.com or www.tevausa.com
The Quality Analyst III will ensure all drug, biologic, and combination products produced by Teva’s Third Party external manufacturing and packaging partners within the Oral Solid Dosage Supplier Relationship Team (SRT) 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.
Monitors supplier KPIs and supports efforts to develop and implement improvements to performance
Follows up with suppliers on quality deviations and ensures that solutions are identified and implemented. Includes supplier audits.
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.
Prepare, negotiate and amend new and existing Quality Technical Agreements.
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.
Review and approve 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
Provide training, support, and guidance to other Quality Analysts
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 5 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, Validations, required.
Experience with external pharmaceutical manufacturing, packaging, and testing is desired.
Able to resolve complex problems and contribute to process improvements
Works independently with minimal guidance
Strong technical writing skills
Strong computer skills including TrackWise, Exel, and SAP is desired.
Senior Third Party Organization Quality Manager, Quality Assurance VI (US Quality)
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 (https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P)
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’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, 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.
EOE including disability/veteran