1+ months

Laboratory Systems Administrator

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.

 

 

Summary:
This position is responsible for the qualification and validation of new laboratory equipment and software. It is also responsible for the day-to-day site administration and maintenance of Standalone Laboratory Computerized systems and interfaces such as FTIR, UV-Vis, Instron Tester, Atomic Absorption, etc. This position provides and/or coordinates problem resolution for users, updates user lists and permissions, reviews audit trails, reviews and updates procedures as needed, administers change controls, and ensures that laboratory standalone computerized systems  are maintained in a validated status in compliance with all regulatory requirements, company policies and procedures.  This position will function as a site subject matter expert for computer system validation, data integrity, etc. and represent the site on corporate 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 qualifying laboratory equipment according to regulatory requirements and site procedures
  • Responsible for identifying/authoring user requirements, functional specifications, risk assessments design specifications, traceability matrix, IQIQPQ documents, etc.
  • Responsible for participating in validation process including creating and/or executing test scripts, revising validation documentation, and reviewing test and change control plans.
  • Responsible for administering change control on computer systems such as activity from user requests, program updates and specification revisions.
  • Responsible for ensuring training of laboratory staff on all end user functions of systems is conducted as needed.
  • Responsible for performing quality review of computer system validation documents and identifying requirements and gaps in the validation process.
  • Responsible for providing technical support and assistance with other relevant computerized systems, especially those in the lab, including designing and executing test scripts and validation activities.
  • Responsible for authoring, editing, reviewing site procedures on equipment operation
  • Responsible for the day-to-day administration and maintenance of standalone laboratory computerized systems
  • Responsible for providing first responder support and coordinating problem resolution as needed for users with issues of a moderate to advanced complexity.
  • Responsible for reviewing and approving configuration changes performed by others.
  • Responsible for creating and managing administrative computer system procedures.
  • Responsible for completing all training requirements and maintaining 100% compliance with all assignments.  
  • Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMPs), Standard Operating Procedures (SOPs) and Batch Record instructions.
  • Supporting other software based laboratory support functions including metrology, stability, purchasing, and inventory/ordering
  • Responsible for performing additional related duties as assigned.

 

Categories

Posted: 2020-03-21 Expires: 2020-06-24

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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Laboratory Systems Administrator

Teva Pharmaceuticals

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