Supplier Quality Engineer

Be part of something altogether life-changing!

Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.

Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.

What you’ll do

• The Supplier Quality Engineer will collaborate with other functional areas and operating entities, including Product Engineering, Quality Assurance, Operations, Supply Chain and Sourcing on all activity required to effectively manage supplier quality requirements & supplier development. Primary areas of focus will be supplier auditing, supplier/part qualification, continuous improvement and supplier change request resolution.
• Improve supplier quality performance for assigned suppliers via Quality Plan implementation
• Ensure Corrective and Preventive Action plans are developed and executed at assigned suppliers in compliance with the CAPA process
• Ensure supplier compliance to Cytiva QMS and regulatory requirements through supplier monitoring process.
• Interface with suppliers and internal stakeholders to drive quality improvements that minimize the Costs of Quality and implement supplier/engineering changes, New Product Introductions and Transfers. Coordinate projects globally for supplier-related issues and collaborations.

Who you are

• Demonstrated ability to lead, develop, communicate & implement a strategy to ensure compliance to Cytiva, regulatory and industry requirements
• Demonstrated technical aptitude: strong background in interpretation of drawings / specifications, measurement method and manufacturing process planning / evaluation
• Effective problem solving, root-cause/CAPA analytical skills to lead and influence others to drive improvement (cross-functionally and globally).
• Excellent communicator and collaborator who can influence at all levels of the organization, both regionally and globally
• Proactive, self-driven, results seeking and enthusiastic intensity, with an eye for quality and compliance
• Experience in supplier quality engineering, quality assurance, quality engineering, manufacturing, or engineering; preferably in the medical device, or pharmaceutical industry
• Degree in an engineering or technical discipline or equivalent non-technical degree with experience in manufacturing, engineering or quality assurance
• Demonstrated knowledge of Quality Management Systems, continuous improvement methodologies and understanding of manufacturing processes
• Knowledge of clean room production and sterility assurance
• Desire and ability to travel up to 30% of the time

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.