1+ months

Associate Director of Quality Systems

Davie, FL 33314
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 in Davie, Florida

 

POSITION SUMMARY
 

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.

 

ESSENTIAL AREAS OF RESPONSIBILITY:

 

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.

Categories

Posted: 2020-04-01 Expires: 2020-06-26

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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