Quality Assurance & Safety category jobs at MRINetwork

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MRINetwork - Encinitas, CA (7 days ago)
Regulatory Affairs Medical Devices There is an immediate need for a Regulatory Affairs Associate or Regulatory Affairs Specialist with experience in medical devices in the Encinitas, CA area. This is an opportunity to join a fast growing company in the class I and class II business. They need someone that understands regulatory reporting, has knowledge of the 510k process and audits either through...
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MRINetwork - Encinitas, CA (7 days ago)
SENIOR QUALITY ENGINEER Medical Device Manufacturing An opportunity exists for a Senior Quality Engineer with experience in medical device project management, process improvement, and new product development in the Encinitas, CA area. The right candidate will have 8+ years in quality assurance with at least 5 of those years in medical device design and/or operations. An extensive knowledge of NPD,...
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MRINetwork - Encinitas, CA (24 days ago)
QUALITY ENGINEER Medical Device Manufacturing There is an excellent opportunity for a Quality Engineer with experience in medical device CAPA and Design Quality in the Encinitas, CA area. The right candidate will have extensive knowledge of CAPA, design controls, and risk assessment. This is an automated high speed manufacturing environment with injection molding, extrusion, and assembly operation...
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MRINetwork - Chicago, IL (35 days ago)
Quality Audit Manager Medical Devices A medical device company in the Chicago, IL area has a need for a Quality Assurance Audit Manager. The position requires 5+ years in the medical device industry and prior success managing audits, CAPA, manufacturing quality, supplier quality, or a similar function where knowledge of medical device manufacturing and compliance to FDA regulations were learned. I...
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MRINetwork - Cincinnati, OH (49 days ago)
Quality Systems Engineer – Quality Documents Medical Devices A medical device company in the Cincinnati, Ohio area has an urgent need for someone with Quality Assurance Document Control experience. The position requires 5+ years in the medical device industry and prior success managing SOPs and strong knowledge of GDPs. Insuring process documentation is accurate and consistent as well as ensuring ...
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