Medical Device Regulatory Affairs Jobs in Indianapolis, IN

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Senior Professional Quality Compliance  

Versiti, Inc. - Milwaukee, WI / Grand Rapids, MI / Indianapolis, IN

4-6 years of experience with a master's degree required Experience in QMS, QA, QC, or Quality Auditing preferably in an environment such as blood banking, pharmaceutical, medical devices

from: milwaukeejobs.com - 4 days ago

Validation Project Manager  

Astrix - Brownsburg, IN, United States

-10+ years of experience in a manufacturing site. Experience in a cGMP environment is an asset. Experience in (medical device) quality & regulatory affairs is an asset. Ability to establish a validation

from: linkedin.com - 11 days ago


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