1+ months

Quality Device Manager

Parsippany, NJ 07054
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
-- Uses best practices and knowledge of internal or external business issues to improve products/services or processes -- Typically resolves complex problems or problems where precedent may not exist -- Often leads the work of project teams; may formally train junior staff -- Works independently -- Requires in-depth knowledge and experience -- Solves complex problems; takes a new perspective using existing solutions -- Works independently; receives minimal guidance -- Acts as a resource for colleagues with less experience -- Represents the level at which career may stabilize for many years or even until retirement

Education and Experience

  • Bachelors degree in Science or Engineering with a minimum of ten (10) years experience in the medical device or combination products field. Background in Mechanical Engineering highly desirable.
  • Must have working knowledge of the QSR CFR Part 820, Part 4, and ISO13485 & 14971 regulations, and desired experience with CFR Part 210/211, ICH and applicable international regulations/guidelines. Knowledge of device regulations relating to drug injection systems and ISO 11608 series - Needle-based injection systems for medical use is highly desirable.
  • Experience with FMEA/risk analysis, Injection molding, syringes, auto-injectors, nasal sprays, and transdermal patches all desired
  • Experience with Quality Systems such as electronic deviation and documentation management systems, SAP, and serialization as well as participation in Quality Councils and Management Review.
  • Experience with external pharmaceutical manufacturing, packaging, testing and devices is desired.
  • Strong computer skills including TrackWise, Oracle and SAP is desired.
Sub Function
Quality Assurance Methods
Reports To

Director Third Party Quality Americas

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.


Posted: 2020-05-18 Expires: 2020-08-30

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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Quality Device Manager

Teva Pharmaceuticals
Parsippany, NJ 07054

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