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.
We are seeking a Supplier Quality Engineer (m/f/d) to ensure exceptional product quality for patient safety, customer value beyond expectations, regulatory assurance, and optimized cost of quality. You''ll be part of a global team, leading all aspects of the supplier management activities related to our Grens plant. Do you have a passion for Supplier Quality? Then we would love to hear from you.
This role will be an onsite position at our Signy Facility (Grens, Vaud).
What you''ll do
Improve Supplier Quality performance for assigned suppliers through Quality Plan implementation.
Approve Supplier Selection & Part/Process implementation through robust qualification processes, including Supplier Audits, Supplier Quality Agreements and Part Quality Plans.
Develop and execute Corrective and Preventive Action plans with Suppliers.
Assure supplier compliance to Cytiva QMS and regulatory requirements through supplier monitoring process.
Collaborate with Suppliers and internal Stakeholders to drive Quality improvements that minimize the Costs of Quality and support implementation of Supplier/Engineering changes, New Product Introductions and Transfers.
Who you are
Degree in an engineering or technical discipline or equivalent non-technical degree with experience in Manufacturing, Engineering or Quality Assurance and with knowledge of Clean- room production and Sterility Assurance.
Demonstrated knowledge of Quality Management System tools, continuous improvement methodologies and in-depth understanding of site level products and related processes.
Qualified Auditor, who can lead, acknowledge, develop, communicate & implement a strategy to ensure compliance to Medical Device requirements.
Effective problem solver, with the skills to lead Root Cause investigations / CAPA plans and influence others cross-functionally.
Able to use French and English as working language, excellent communicator and collaborator who can influence at all levels of the organization.
Join our winning team today. Together, we''ll 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.
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