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
 
Monitors and supervises the documentation function by reviewing incoming inspection reports through to product release to ensure compliance with current good manufacturing practices and FDA regulation requirements.

 

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.

 

 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), Standard Operating Procedures (SOPs) and Batch Record instructions.
 Responsible for completing all training requirements and maintaining 100% compliance with all assignments.  
 Supervises, coordinates and prioritizes the daily activities of the Quality Assurance Documentation Department and assigned staff.
 Reviews data to assure conformance to product specifications and maintains quality assurance objectives to meet corporate policies and goals.
 Implements batch records review criteria and procedures and maintains documentation on all manufacturing batch records and related documents.
 Supervises and monitors employees engaged in record review and release and issuance of batch records.
 Participates in quality management teams within organization.
 Ensures project deadlines and performance standards are established and met.
 Responsible for performing additional related duties as assigned.

Categories

Posted: 2020-04-28 Expires: 2020-06-30

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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Group Leader Quality Assurance

Teva Pharmaceuticals

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