Siemens Healthineers
Healthcare Insurance • Biotechnology • Medical Device
Siemens Healthineers is a leading MedTech company focused on pioneering breakthroughs in healthcare. They offer a comprehensive portfolio that addresses the entire care continuum for serious diseases, including medical imaging, laboratory diagnostics, point-of-care testing, and digital health solutions. With a commitment to innovation, sustainability, and improving patient access to care, Siemens Healthineers collaborates with healthcare professionals and organizations globally to advance medical technology and enhance patient outcomes.
10,000+ employees
⚕️ Healthcare Insurance
🧬 Biotechnology
💰 $1.5M Grant on 2021-05
Director – Chemistry Commercial Product Quality
October 15
Siemens Healthineers
Healthcare Insurance • Biotechnology • Medical Device
Siemens Healthineers is a leading MedTech company focused on pioneering breakthroughs in healthcare. They offer a comprehensive portfolio that addresses the entire care continuum for serious diseases, including medical imaging, laboratory diagnostics, point-of-care testing, and digital health solutions. With a commitment to innovation, sustainability, and improving patient access to care, Siemens Healthineers collaborates with healthcare professionals and organizations globally to advance medical technology and enhance patient outcomes.
10,000+ employees
⚕️ Healthcare Insurance
🧬 Biotechnology
💰 $1.5M Grant on 2021-05
📋 Description
• Responsible for leading the CLS Chemistry Commercial Product Quality (CPQ) Team • Ensuring compliance with applicable regulations and standards • Drive product safety, product quality, and customer satisfaction related decisions • Establish short- and long-term goals to improve complaint resolution, product reliability, and customer satisfaction • Training and development of group members • Driving continuous improvement and excellence in results for Key Performance Indicators (KPIs)
🎯 Requirements
• Typically, 8+ years of successful experience in related field • Direct experience in the in-vitro diagnostics industry • Strong knowledge in complaint handling, investigations, medical device reporting, field action and CAPA processes. • Detailed understanding of FDA 21 CFR 820, 21 CFR 803, 21 CFR 806, ISO 13485, MDSAP, and EU IVDR requirements. • Strong technical knowledge of supported product lines. • BS/BA in related discipline, or advanced degree, where required, or equivalent combination of education and experience.
🏖️ Benefits
• medical insurance • dental insurance • vision insurance • 401(k) retirement plan • life insurance • long-term and short-term disability insurance • paid parking/public transportation • paid time off • paid sick and safe time
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