10 days old

Quality Auditor Associate/(N2 shift) Fri-Sun & E/O Thur, 6:00 PM to 6:30 AM

Salt Lake City, UT 84111
Company Info

Teva is a global pharmaceutical leader and the worlds 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 worlds largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and weve 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.). This position is located at our facility in Research Park, near the University of Utah (575 Chipeta Way, 84108). For more on Teva, check us out at www.tevapharm.com or www.tevausa.com.

 

Key Responsibilities:

Under close supervision, conduct AQL inspections on products and conducts GMP audits. Review completed intermediate commercial batch records as well as non-commercial experimental records. Resolve GMP issues on the production floor.  Issues batch records and all supporting documents per the manufacturing master schedule.  Performs sampling activities associated with the commercial manufacturing core, including retain, analytical, and complaint samples. This position is scheduled to work 6:00 am to 6:30 pm, Fri-Sun and every other Thursday.

  • Responsible for the performing issuance of batch records and supporting documents for commercial and non-commercial batches manufactured in the 575 production core.
  • Responsible for performing sampling and delivery of intermediate and finished products.
  • Responsible for conducting monthly GMP and batch-specific room audits.
  • Responsible for performing in process record review of commercial manufacturing batch records.
  • Responsible for reviewing completed documentation associated with intermediate and finished products; prepare documentation for final disposition.    Responsible for reviewing completed swab data and performing subsequent room/equipment release.

 

Education:

  •  High school diploma or GED

Experience:

  • Observing and identifying problems, assisting in resolution to support Company goals.
  • Reading, interpreting records, reports, business, personal and scientific computer data, certificates of analysis and conformance and other applicable data sources
  • Responding to inquiries from management, employees and regulatory agencies under direction of management.
  • Communicating clearly and concisely, both orally and in writing.
  • Operating scientific, business and personal computers.

Knowledge:

  • Current Good Manufacturing Practices (cGMP), Food and Drug Administration  (FDA), and other regulatory requirements.
  • Principles of auditing.
  • AQL sampling and inspection principles and techniques.
  • Principles of mathematical computations.
  • Business, scientific and personal computer hardware and software applications.

Categories

Posted: 2019-11-07 Expires: 2019-12-16

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.

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:

Quality Auditor Associate/(N2 shift) Fri-Sun & E/O Thur, 6:00 PM to 6:30 AM

Teva Pharmaceuticals
Salt Lake City, UT 84111

Join us to start saving your Favorite Jobs!

Sign In Create Account
Powered ByCareerCast