2 Medical Device Regulatory Affairs Jobs in Spencer, IN
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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 11 days ago
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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 4 days ago
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