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The opportunity
The role is accountable to ensure deliverance of revenue and free cash flow for complex products (including combination products) within the EMSO Americas division, including committed Customer Service Levels and On-Time In-Full (OTIF) targets, while ensuring compliance targets. They are accountable to manage the quality activities for the device components, drug components and finished products produced by Teva’s Third Party external manufacturing and packaging partners. They are accountable to ensure the product meets established standards of quality including reliability, usability, and performance. Ensures ongoing compliance with quality and industry regulatory requirements for 21CFR 820 and 21CFR Part 4, as well as 21CFR Parts 210/211.
How you’ll spend your day
Collaborate with suppliers to ensure their compliance and the quality of their products, materials, components and/or operations. 
Analysis and development of specifications and test methods with both external and internal business partners (change controls, release documents, and other applicable documentation) to confirm and sustain compliance to 21 CFR Parts 4, 210 and 211.
Review, evaluate and approve change controls from Third Party Suppliers and act as the point of contact for all comments between internal departments and the site. 
Manage product quality complaint investigations and determine if regulatory notification (ex. FAR or BPDR) is required. 
Development and presentation of product data to management in support of changes. Maintenance of product files. 
Participate in Quality Councils and Management Review for SRT, including tracking and managing actions for Complex products. 
Manage KPIs and prepare presentations for Complex meetings as required. 
Visit CMOs to resolve critical issues, including audits of products. 
Receive and review quality customer complaint investigations, nonconformance reports and laboratory investigations, ensuring all necessary components are included.  
Ensure annual stability testing is being performed as per regulatory requirements. 
Compile data from third party suppliers for the preparation of annual product review. 
Participate in root cause analysis and prepare written investigations for deviations/NCRs. Follows up with suppliers on quality deviations and ensures solutions are identified and implemented, including those from supplier audits. 
Attend all daily/weekly operational and quality meetings in support of Complex products. 
Development of processes and procedures to support QMS.