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JO
Senior Regulatory Affairs Specialist (f/m/d)
jobs.danaher.com · Kraków, Poland
About The Role
Join our team as a Senior Regulatory Affairs Specialist and play a key role in ensuring global compliance for medical devices. Leverage your expertise in regulatory standards and ISO 13485 to support audits, manage product change control, and drive quality initiatives. Make a real impact in life sciences and diagnostics with Cytiva.
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