1+ months

Quality Analyst III

Davie, FL 33314
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

Under limited supervision, this position is responsible for coordinating investigations into product complaints.  Authors and compiles Annual Product Reviews and generates quarterly and yearly Quality Review Reports.  Monitors and trends key areas and indicators from production and laboratories for implementation of corrective and preventative measures.

Carries out responsibilities in accordance with the organizations policies, procedures, and state, Federal and local laws.
Responsible for complaint investigations; assist with weekly and monthly metrics.
Provide sub reports for APR, annual product review.
Process change controls and update as needed.
Prepare APR report to show product performance, validation status and determine compliance.
Prepare monthly and quarterly APR metrics for Quarterly Council.
Coordinate with other department to complete investigations and reports.
Create quarterly APR schedule.
Attend Quality Council meeting and prepare meeting minutes.
Responsible for submitting change control.
Responsible for completing investigations.
Participates in Audits.
Review and approve documents in trackwise, (Deviations, CAPAS, LIR, and effectiveness check).
Review and approve protocol reports, change control and cleaning validation.
Provide guidance and coaching to employees.
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), and Standard Operating Procedures (SOPs) instructions.
Responsible for performing additional related duties as assigned.


Bachelor Degree in Science, Engineering or related field from an accredited college or university, and a minimum of five (5) years related experience preferably in a quality assurance environment.

Sub Function
Manufacturing Quality Assurance
Reports To

QA Manager

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: 2020-09-17 Expires: 2020-11-14

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 III

Teva Pharmaceuticals
Davie, FL 33314

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