Sr Dir Plant/Site Quality I
Company: Teva Pharmaceuticals
Posted on: December 6, 2018
Ensure that a Quality Management System is in place, securing compliance of activities and supporting continuous improvement.
Lead Quality Regulatory Compliance Provide guidance to site managers and employees, conduct internal and support external audits, to ensure compliance with Teva's global standards, regulatory guidelines and cGMP requirements.
Main Responsibilities & Deliverable
Assess and Mitigate Risks Identify quality risks and define proactive mitigations, to ensure the products are safe and effective before they reach the market. Work with the business to assure compliant and reliable supply.
Design and Implement the Site Quality Program In collaboration with the site GM and Corporate Quality, create, implement, monitor and update the site quality program.
Manage Quality Data Oversee the delivery of necessary data to site managers and supervisors, Corporate Quality and other relevant internal and external stakeholders, in order to support the achievement of Quality objectives and ensure compliance.
Direct Quality Control Oversee the laboratory activity, including analytical site transfers, testing and approval or rejection of raw materials, packaging materials, in process materials and finished products for the site.
Promote a Sustainable Culture of Quality Create, develop and maintain a culture of enhancing quality throughout the entire site operation. Create a space where people can speak openly and are encouraged to present new ideas to improve quality.
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!
Bachelor's Degree* - engineering or related science-based degree. Master's Degree - in science, business, healthcare, or an equivalent combination of education and experience related to Quality Assurance/Quality Control - advantage at large and complex sites. Professional certifications a must when required legally.
Quality Assurance Methods
In process of validation
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, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.
Nearest Major Market: Irvine California
Nearest Secondary Market: Los Angeles
Keywords: Teva Pharmaceuticals, Irvine , Sr Dir Plant/Site Quality I, Professions , Irvine, California
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