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Manager Quality Assurance

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! Job Description The primary responsibility of the Commercial Quality Assurance Distribution Center Manager  is to ensure that products manufactured by Teva Operations sites and 3rd party manufacturers are supplied to customers and patients in full compliance with Regulations and  and Teva's global standards. Represents the quality function within the local pharmaceutical license holders and communicates with local and regional competent health authorities. Coordinates Quality Improvements, serves as the Subject Matter Expert on activities related to the cGMPs of the Warehouses and Distribution Centers at Teva. Review and approve procedures, validations, deviations and change controls associated with the Warehouse and Distribution Centers. Coordinates with relevant Teva functions, markets and competent authorities' investigations and follow up actions for quality events. Qualifications Undergraduate/BA/BS degree in Chemistry, Biology, Microbiology, Pharmaceutical Sciences, Nursing, or associated scientific discipline or undergraduatedegree in other discipline but with at least 5 to 7 years working experience in cGMP regulated environment. Experience with cGMPs, good written and verbal communication skills, and ability to work independently and managing multiple possibly conflicting priorities are required to perform the job.   5-7 years of related experience in Pharmaceuticals/Pharmaceutical QA. This experience could be obtained within the Pharmaceutical/Medical Device/Biopharmaceutical industries and/or within other highly regulated industries.  Experience at a pharmaceutical/biopharmaceutical/medical device manufacturing/packaging/testing facility is especially useful and desired. Experience with manufacturing, packaging and laboratory testing of different dosage forms is beneficial and highly desired Advanced Skills and Ability to clearly speak (and understand) English Language is required to perform the job. Customer Service/Customer Satisfaction skills and abilities are required to perform the job.     These English Language skills and abilities could be obtained through normal educational schooling.  The Customer Service skills and abilities could be obtained through previous jobs in the service sector Training/experience in manufacturing, packaging and laboratory testing of different dosage forms is beneficial and highly desired.  
Salary Range: NA
Minimum Qualification
5 - 7 years

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