Senior Quality Project Engineer

Bring more to life.     Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?      At   Cytiva , one of   Danaher’s   15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.       You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And   by harnessing   Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.     Working at   Cytiva   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. Take your next step to an altogether life-changing career.     Learn about the   Danaher Business System   which makes everything possible.   The Senior Quality Project Engineer is responsible for providing quality leadership for business-initiated projects, including New Product Development (NPD), product sustainment, customization, innovation initiatives, and Transfer of Work (ToW) activities. As a core member of cross-functional project teams, the Senior Quality Project Engineer represents the Quality function and ensures that quality, regulatory, and compliance requirements are effectively integrated throughout the entire product and process lifecycle. This position reports to the Director QA – Single Use Technologies, Projects and Continuous improvement and is part of the Upstream and Fluid Management QA & RA organization located in Hoegaarden, Belgium and will be an on-site role.

Provide quality oversight and guidance throughout design transfer, process development, verification, validation, and commercialization activities. Support successful transfer of products and processes from development to routine manufacturing, establishing robust quality controls and monitoring strategies to ensure consistent product quality and process performance. Partner with Product Management, RD&E, Manufacturing Engineering, Regulatory Affairs, Supply Chain, Supplier Quality, Global Sterility Assurance and Operations to support robust product and process development while ensuring successful project execution Author, review, approve, and maintain validation protocols, reports, and other quality-related project documentation in compliance with applicable procedures and standards. Leverage complaint investigations, CAPAs, non-conformances, audit observations, and other quality data sources to drive continuous improvement and strengthen quality-by-design principles within product development activities Who you are: Master or bachelor’s degree in applicable field or equivalent by experience in Quality in a similar (GMP)/ISO regulated BU/Industry. 5 + years of relevant quality experience of which at least 3 years of applicable industry experience. Can work independently as a quality lead within a cross-functional team to support successful implementation of new projects and products. Validation/qualification experience and project management are a must. Strong working knowledge of quality assurance principles and practices, industry and international regulations and standards (ISO9001 and/or ISO134585). Travel, Motor Vehicle Record & Physical/Environment Requirements: Ability to travel 5-15% (domestic and international). It would be a plus if you also possess previous experience in: Knowledge of ISO11137, ISO14644 and ISO14698 is a plus. Statistical improvement tools and lean manufacturing techniques. Join our winning team today. Together, we’ll accelerate the real-life