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Were you looking for ISO13485-21CFR820 job results?
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Online Resumes with "ISO13485 21CFR820"
Engineering Manager - 10+ years experience - ISO-13485, 21 CFR 820/211, cGMPs, Lean/Six Sigma, Project Management.
To obtain a management level Engineering/Manufactiring/Operations within regulated Medical Devices/Biotech/Pharma/Food Industry where I can utilize past experience in Manufacturing support, process developement, process improvement and product sustaining.
Tags for this Online Resume: Six sigma , Project Management, cGMPs, Lean Manufacturing, APQP, Seasoned Manager
Mechanical Inspector- L-3 Communications 5 yrs- Ca
CMM Inspector, Opg , ISO-9000 and ISO-13485,21 CFR820, Mil-std
Biomedical Engineer - 20 Years of Experience - Near 94025
Key start-up contributor. Extensive knowledge of medical device development and manufacturing. Experienced with distilling physician interactions into new product ideas, assessing new tech/Market, Feasibility and Prototypes. Tenacious, out of the box thinker. Willingness to pitch in to both critical and mundane projects necessary to the company. Visionary innovator/manager with extensive experience in medical products acro...
Tags for this Online Resume: Product Development, ISO13485 21CFR820, Medical Devices, V, Prototyping, Research , Process Development, Commercial release
