Teva Pharmaceuticals Quality Analyst III in Copiague, United States
Quality Analyst III
Date: Apr 16, 2019
Location: Copiague, US, 11726
Company: Teva Pharmaceuticals
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.
This position is located in 33 Ralph Ave, Copiague, NY 11726
For more on Teva, check us out at www.tevapharm.com at http://www.tevapharm.com/ or www.tevausa.com at http://www.tevausa.com/ .
Under general supervision, coordinates 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.
This is not intended as a comprehensive list; it is intended to provide a representative summary of the major duties and responsibilities. Incumbent(s) may not be required to perform all duties listed, and may be required to perform additional, position-specific tasks.
Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws.
Analyzes data from production and laboratories, and reports anomalies.
Monitors activities in key areas for compliance to standards and opportunities for improvement.
Coordinate investigations and writes final reports for product complaints. Authors Annual Product Review reports. Generates quarterly and yearly Quality Review Reports. Guides QA Engineer Associate in conducting job responsibilities.
Researches and recommends improvements in production and laboratory systems.
May review, approve and support execution of validation protocols and master plans.
Complies with all company policies and procedures, including safety rules and regulations. Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements in a regulated manufacturing environment.
Performs related duties as assigned.
Bachelor's Degree in Science, Engineering or related field from an accredited college or university.
Minimum of two (2) - four (4) years related experience preferably in a quality assurance environment; or, an equivalent combination of education and/or experience.
Quality Assurance Methods
Manager, QA Documentation
Teva’s Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.
Nearest Major Market: Long Island
Nearest Secondary Market: New York CIty
EOE including disability/veteran
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