1+ months
Company Info

If youre like people at Teva, you dare to be different. Were making well-being a way of life for our customers and our colleagues. Join us in helping to make healthcare more accessible to more patients, while supporting one of the most innovative teams in the industry.


Tevas Davie and Sunrise (Florida) production sites are two of our largest launch facilities.   We are strengthening and adding to our critical teams with great talent and capabilities. Teva, a global organization, with a brand of evolving success.  Be part of it!


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


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 we have 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!

Job Description

*Shift Work Will Be Required For This Position*

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.


 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.

*Shift Work Will Be Required For This Position*



Bachelors Degree in a Science related field or equivalent curriculum; or equivalent and minimum five (5) years quality assurance manufacturing and/or quality assurance warehouse environment experience OR minimum five (5) years of satisfactory performance as a Quality Assurance Inspector IV.

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

Sub Function
Manufacturing Quality Assurance
Reports To

Assoc Dir, QA - Operations & Batch Release

Already 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 Site

The 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.


Posted: 2020-08-10 Expires: 2020-11-12

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

Teva Pharmaceuticals
Davie, FL 33314

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