1+ months

Quality Specialist III

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 the International Center, near the Salt Lake City International Airport (4745 Wiley Post Way, 84116). For more on Teva, check us out at www.tevapharm.com or www.tevausa.com.

 

Position Requirements:
This position has the responsibility to assist and support all Document control functions in a pharmaceutical environment.  This person will assist in ensuring compliance with regulatory requirements and will interact with all areas within the company to ensure that change control policies are followed with a high level of accuracy.

 

Responsibilities:
All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other related duties or assignments.

  • Responsible for ensuring document control and regulatory compliance with emphasis on document management in pharmaceutical production.
  • Assist in coordination of the review and revision of controlled documents (master batch records, procedures, specifications, test methods and forms).  Ensure consistency in format and presentation of content for all documents.
  • Help to ensure adequate and compliant document change control practices.
  • Assist in organizing and maintaining files for all master documents and document history.
  • Assist in compiling regulatory filing documents.
  • Issue documents, binders and batch records to appropriate personnel, in a timely manner.
  • Effectively interact with other functional groups (e.g., Production, VCTS, external regulatory affairs, etc.)
  • Responsible for performing day-to-day tasks that occur in a Document Control Function (typing, filing, research, etc.) without immediate and constant supervision.
  • Assist in coordinating activities related to the implementation and maintenance of an EDMS (electronic document management system).

 

 

Categories

Posted: 2019-11-01 Expires: 2020-01-05

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 Specialist III

Teva Pharmaceuticals
Salt Lake City, UT 84111

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