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Supvervisor Quality Assurance Documentation

Company: Teva Pharmaceuticals
Location: Salt Lake City
Posted on: March 28, 2020

Job Description:

Supvervisor Quality Assurance DocumentationDate: Mar 23, 2020Location: Salt Lake City, Utah, US, 84106Company: Teva PharmaceuticalsCompany 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 .Job Description Position Summary:This position is responsible for providing oversight, guidance, training and direction to the Quality Assurance Documentation unit, which supports all commercial and R&D units in the facility. This position is responsible for several key quality systems, including EDMS, Change Control, Master Record Maintenance and Third Party document tracking and approvals. This position is responsible for labeling specification changes on new product launches, as well as facilitation of documents to support other departments. The Quality Assurance Documentation Supervisor coordinates periodic reviews for all documents, monitors and reports department metrics and manages within AOP, along with other special projects as assigned.Essential Functions:Task/Function to be executed and perecentage of time:

  • Change Control-20%
  • Third Party Liaison-30%
  • Project Support-20%
  • Annual Reports for India RA and Third Parties-20%
  • Access requests for Trackwise Harmony and Livelink. Oversee training on new systems-20%
  • Metrics-10%Qualifications Experience:
    • Five years experience in a document control department with an understanding of a regulated industry such as medical device or pharmaceuticals
    • High school diploma requried; Associate Degree preferred
    • Familiarity with EDMS, TrackWise and Microsoft Office Suite
    • Ability to understand and follow Teva Corporate Policies and department standard operating procedures
    • Understanding of regulatory agencies expectations, including CFRs applicable to the pharmaceutical industryFunction QualitySub Function Quality Assurance MethodsReports To In process of validationAlready 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 SiteThe 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.Tevas 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.EOE including disability/veteran

Keywords: Teva Pharmaceuticals, Salt Lake City , Supvervisor Quality Assurance Documentation, Other , Salt Lake City, Utah

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