Internal Quality Audit Medical Device Jobs in Hopkinton, NH

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Medical Device - Regulatory Affairs and Quality Assurance Manager  

Cambridge Interventional - Burlington, MA, United States

compliance activities including complaint handling, recalls, medical device reporting and import/export requirements. · Prepare and execute internal quality audits for the Company. · Oversees product/process

from: linkedin.com - 17 days ago

Sr. Manager, Quality Assurance  

EPM Scientific - Billerica, MA, United States

readiness for both internal and external audits Qualifications: Bachelors degree with approx. 8-10 years of Quality experience in medical device, combination product experience preferred Direct experience

from: linkedin.com - 21 days ago

Staff Advanced Quality Engineer (Hybrid)  

Stryker - Shirley, MA

Engineers to develop robust verification test strategies. Analyze failures using root cause analysis techniques. Perform supplier development activities, including PPAP. Conduct internal quality system audits

from: Dice.com - 17 days ago

Senior Supplier Quality Engineer  

Johnson and Johnson - Danvers, MA

devices, aerospace). Risk Management: Identify and mitigate quality and supply chain risks associated with supplier activities. Collaboration: Work closely with internal departments such as procurement

from: Johnson and Johnson - 8 days ago

Staff Supplier Quality Engineer  

Johnson and Johnson - Danvers, MA

in regulated industries (e.g., medical devices, aerospace). * Risk Management: Identify and mitigate quality and supply chain risks associated with supplier activities. * Cross-functional Collaboration: Work

from: Johnson and Johnson - 8 days ago

Sr Technical Writer - Abiomed  

Johnson & Johnson - Danvers, MA

and/or writing, medical device experience preferred. 5+ years of technical documentation or quality engineering experience Ability to communicate ideas and information clearly, effectively, and frequently (oral

from: Dice.com - 14 days ago

Senior Quality Engineer  

Katalyst Healthcares & Life Sciences - Wilmington, Massachusetts

resulting from quality events, audits, or regulatory changes to ensure compliance with FDA 21 CFR 820. Assisting in the development of the company quality system to support medical device offerings

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from: resume-library.com - 24 days ago

Director of Regulatory and Quality  

Michael Page - Danvers, MA

manufactures and markets various electronics, consumables, and services that enable breakthroughs in within their Medical Device market. They have a growing diversified portfolio of customers which $160,000 - $180,000/Year

from: careerbuilder.com - 19 days ago


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