1+ months

Associate Director of Quality Systems

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 general direction, oversees all aspects of Quality Systems of the Quality Assurance Department related to the manufacturer of products in strict accordance with all Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs), Company policies and procedures, and Food and Drug Administration requirements governing the manufacture of pharmaceutical products.  This role will manage the CAPA and Deviation Program at the site. The Quality Engineering team will report into this position.




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.


 Manages the deviation and CAPA system at the site. 
 Responsible for the management of the Quality Engineering Team at the site.
 Oversees and manages all Quality Systems of the Sunrise and Davie Manufacturing sites such as closure of deviations, CAPAs, change controls, and other Quality documentation.
 Ensures compliance of the site to the Quality Systems and manages the on time completion of Quality System actions.
 Manages and ensures CAPAs are handled in a timely manner in accordance with Teva SOPs and regulatory requirements.
 Oversees, manages, coordinates and prioritizes the daily activities of the Quality Assurance Department and assigned staff to include the Quality Engineering team as required.
 Ensures department compliance with and enforcement of SOPs and cGMPs.
 Reviews and approves production and process control SOPs that are drafted, reviewed and approved by other organizational units.
 Reviews and approves deviations, CAPAs, Change Controls and other Quality System documentation.
 Is responsible for the oversight of effectiveness checks.
 Manages the identification, investigation, and closeout of manufacturing deviations to include escalations to management.
 Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, cGMPs, SOPs and Batch Record instructions.
 Responsible for completing all training requirements and maintaining 100% compliance with all assignments.  
 Oversees, participates and approves the interviewing, hiring, and training, of departmental employees; conducts performance evaluations for direct reports; and assists direct report supervisors with performance evaluation process for their units.
 Provides support, direction, and coaching to subordinate employees in the areas of disciplinary action, problem resolution, planning, and work assignment delegation.
 Ensures project deadlines and performance standards are established and met.
 Responsible for performing additional related duties as assigned.



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



 Requires Bachelor Degree in Science, Engineering or related field from an accredited college or university. 
 Minimum of seven (7) years relevant progressive experience in the pharmaceutical industry, including a minimum of three (3) years in supervisor or managerial capacity.
 Preferably in a pharmaceutical manufacturing environment.

Sub Function
Manufacturing Quality Assurance
Reports To

Senior Director, Quality Lead

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: 2020-04-01 Expires: 2020-08-14

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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Associate Director of Quality Systems

Teva Pharmaceuticals
Davie, FL 33314

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