Medical Devices Jobs in Cincinnati, OH

Vapotherm - Cincinnati, OH, United States

, Computer Science or local equivalent of same; generally, 7-10 years of experience Experience with Medical Devices, FDA Regulations, ISO 13485, and IEC 62304 required Experience in at least one complete

from: linkedin.com - 14 days ago

Gus Perdikakis Associates - Cincinnati, OH, United States

assembly) Worked in: Consumer Products Medical Device Automotive Ancillary experience (any depth): Project Management (schedule creation and management) Cross functional engagement with: Quality Supply Chain

from: linkedin.com - 2 days ago

Blake Smith Staffing, LLC - Cincinnati, OH, US

0-2 years successful similar sales experience, within the United States Department of Veteran Affairs, calling on VAMC and CBOC networks...

from: jobvertise.com - 11 days ago

Vapotherm - Cincinnati, OH, United States

will apply expert technical knowledge and multi-disciplinary engineering principles to translate customer needs into innovative solutions within established medical device regulations and applied standards

from: linkedin.com - 14 days ago

Vapotherm - Cincinnati, OH, United States

principles Apply technical competency towards innovative, complex medical device development Develop and document detailed design specifications and acceptance criteria Design, build, and test prototypes

from: linkedin.com - 14 days ago

Meridian Bioscience, Inc. - Cincinnati, Ohio

Must be able to empathize with the customer, understand customer needs, act in an urgent manner to resolve customer issues and raise...

from: resume-library.com - 24 days ago

HCLTech - Cincinnati, OH, United States

and guidelines with medical devices. (e.g., FDA 21 CFR Part 820, ISO 13485). 9. Strong communication and collaboration skills, with the ability to work effectively in a team environment. 10. Excellent analytical

from: linkedin.com (+1 source) - 24 days ago

Gateway Recruiting - Gateway to Global Careers - Contingent, Retained, Contract Recruiting Services - Cincinnati, OH, United States

SUMMARY: The Director of Quality Assurance and Regulatory Affairs ensures continued regulatory conformity to FDA 21CFR820, ISO13485, ISO14971, and EU Medical Device Regulation (EUMDR). This position

from: linkedin.com - 29 days ago

Johnson and Johnson - Cincinnati, OH

/ The Senior Principal Engineer will operate as an expert in equipment, assembly, and automation technologies across J&J MedTech Supply Chain. They will bring new, unique, and ground-breaking medical device

from: Johnson and Johnson - 3 days ago

Integrated Resources, Inc - Cincinnati, Ohio

is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices markets. Employees

from: resume-library.com - 3 days ago