1+ months
Company Info

Teva is a global pharmaceutical leader and the world's 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 world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've 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. For more information on Teva, check us out at www.tevapharm.com or www.tevausa.com

This position is located on 4001 SW 47th Ave, Davie, FL 33314

 

POSITION SUMMARY
 
Under minimum supervision, ensures compliance to cGMP regulations in manufacturing area including all documentation complying with the companys Standard Operating Procedures (SOPs), governmental regulations and other requirements where applicable.  Provide support to operations by leading operations oversight and resolution of quality events. Communicate effectively with cross functional departments to resolve quality events in a timely manner.


ESSENTIAL AREAS OF RESPONSIBILITY


 Carries out responsibilities in accordance with the organizations policies, procedures, and state, Federal and local laws.
 Perform on floor audits of manufacturing records, logbooks and other applicable documentation
 Perform daily operations GMP walkthroughs
 Lead and work collaboratively with site operations in the resolution of quality events and deviations by supporting/ completing the Event Response Team (ERT) Form, determining product impact and ensuring compliance with GMPs and SOPs.
 Review and approve work orders for equipment and facility 
 Assist in the training of new Inspectors in job duties according to Standard Operating Procedures (SOP), current Good Manufacturing Practices, (cGMP) and Company training procedures.
 Verifies and revise QA SOPs as required
 Maintains QA documentation files, database and logs.
 Prepares change controls for SOPs.
 Responsible for performing additional related duties as assigned.

Categories

Posted: 2020-03-27 Expires: 2020-07-04

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 Engineer

Teva Pharmaceuticals

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