Customer Success Analyst
About Us:Establishment Labs is changing the medical device, breast health, aesthetics and reconstruction industry by designing, developing, and manufacturing an innovative portfolio of advanced medica...
Explore 10 active Mdsap job openings aggregated from hundreds of sources. Roles range from entry-level to executive, remote and on-site, refreshed hourly.
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About Us:Establishment Labs is changing the medical device, breast health, aesthetics and reconstruction industry by designing, developing, and manufacturing an innovative portfolio of advanced medica...
About Us:Establishment Labs is changing the medical device, breast health, aesthetics and reconstruction industry by designing, developing, and manufacturing an innovative portfolio of advanced medica...
What if the work you did every day could impact the lives of people you know? Or all of humanity? At Illumina, we are expanding access to genomic technology to realize health equity for billions of pe...
**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfu...
Vacancy description The MDR Lead Auditior performs independent audits against the Medical Devices Regulation (MDR), ISO 13485, MDSAP, UK Medical Devices Regulation, in accordance with established proc...
Location: Ruhrgebiet, Hamburg or Berlin Employment: Full-time, unlimited Your tasks Co-responsibility for the strategic further development and future security of an international department in the fi...
About UsIkerian AG (formerly RetinAI Medical) is a fast-growing medical device software company headquartered in Bern, Switzerland. Our mission is to enable the right decisions sooner in healthcare, t...
We are looking for an experienced Specialist in the field of Quality Management and Regulatory Affairs (m/w/d) for our customer, a future-oriented company in the medical technology sector. Your Tasks...
Job Description Main Purpose of Role To centrally manage a Lean and compliant Quality Management system for medical devices schemes (Medical includes Notified Body NB1639, UKCA, ISO 13485, MDSAP and a...
Key requirements Good knowledge of ISO 13485 (for medical device) Good knowledge of product registration - in the EU (familiar with CE Mark, MDD, MDSAP, MDR) Responsibilities: To act as Person Respons...
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