1+ months

Quality Analyst I

Salt Lake City, UT 84111
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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.
 

 

This position is responsible for providing Quality Assurance support to Manufacturing, Supply Chain and Quality Control Laboratories by providing QA review and approval of new and existing methods/procedures, validation/transfer protocols, investigation documentation, and process/facility change control documents.  This position supports teams using trend and investigational data to create value through process improvements and failure reduction activities, and provides representation for quality department on cross functional teams. 

 

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 providing a thorough and timely review and approval of cGMP documents and processes such as those related to validation, change documentation, deviations, investigations, equipment and facilities qualifications, protocols and reports, and facility controls, instruments and procedures.
  • Responsible for review and approval of activities in the site change control systems.
  • Responsible for providing first response and ongoing QA presence for quality and compliance issues on the manufacturing floor and as needed in the laboratories.
  • Responsible for compiling and maintaining metrics and tracking logs for sites quality KPIs or other functions.

 

 

Requirements:

Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered.
 

Education/Certification/Experience:

  • Requires a Bachelors Degree or equivalent in Science or Engineering with a minimum of four years relevant progressive QA experience in the pharmaceutical or a related industry.
  • Requires experience with and an in-depth knowledge of cGMP and other applicable industry regulatory requirements as they relate to the production of pharmaceutical products and associated quality systems.
  • Requires working knowledge of the handling of deviations, investigations and CAPAs.
  • Experience in a solid dose manufacturing environment preferred.
  • Experience with Manufacturing/Quality systems such as Trackwise, LIMS/Labware, Crystal Reports, Learning Management Systems and statistical software preferred.
  • Experience with laboratory related investigations/inquiries preferred.

 

Skills/Knowledge/Abilities:

  • Detail oriented with ability to analyze information and create corresponding performance metrics.
  • Computer proficiency with comprehensive working knowledge of MS Office products and computer relational databases.
  • Ability to demonstrate sound judgment and decision making.
  • Ability to build and maintain collaborative relationships between teams, departments and business units.
  • Communicate effectively with excellent written and oral communication skills.
  • Interact positively and collaborate with co-workers, management and external partners.
  • Manage conflict and negotiate resolution.
  • Self-directed with ability to organize and prioritize work.
  • Project management and advanced presentation skills a bonus.

Posted: 2019-12-27 Expires: 2020-03-12

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 Analyst I

Teva Pharmaceuticals
Salt Lake City, UT 84111

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