Medical Device Engineering Jobs in Westborough, MA
CONMED Corporation - Westborough, MA, United States
, mechanical, manufacturing, electrical, quality, R&D, etc) Passionate about Engineering and the medical device industry 0-20% travel These future opportunities are not eligible for employer-based sponsorship
from: linkedin.com - 8 days ago
Kelly Science, Engineering, Technology & Telecom - Westborough, MA, United States
that are designed to mitigate the risks identified through the Risk Management process. Qualifications: Bachelor’s degree 5 years Quality Assurance/Quality Engineering experience in the medical device
from: linkedin.com (+1 source) - 29 days ago
Olympus Corporation of the Americas - Westborough, MA, US
of the requirements setting, design testing, and validation stages of physical and digital medical devices. Ensure that expert HFE input is provided to product design teams and the Regulatory team for addressing design
from: Olympus Corporation of the Americas - 6 days ago
Kelly Science, Engineering, Technology & Telecom - Westborough, MA, United States
in the medical device or pharmaceutical industry Demonstrated understanding or aptitude to understand Medical Device QMS requirements and regulatory requirements including but not limited to FDA CFR 21 820 and ISO
from: linkedin.com - 29 days ago
Olympus Corporation of the Americas - Westborough, MA, US
for Quality System issues All Other Essential Duties as assigned by Management. Job Qualifications Required: Bachelor of Science, medical, engineering, or scientific discipline Minimum of 5 years’ experience
from: Olympus Corporation of the Americas - More than 30 days ago
Olympus Corporation of the Americas - Westborough, MA, US
of professionalism, ethics and compliance at all times. Job Qualifications Required: Bachelor's Degree in Engineering required. Minimum of 5 years of experience in Quality Engineering within an FDA regulated medical
from: Olympus Corporation of the Americas - 18 days ago
Digital Prospectors - Marlborough, MA, United States
will translate product requirements into design specifications, managing system engineering activities in an FDA regulated environment, and ensuring compliance with quality standards for medical devices. Essential
from: linkedin.com - 7 days ago
Olympus Corporation of the Americas - Westborough, MA, US
products in compliance with FDA and international requirements, including 820-CFR, ISO14971, IEC60601, GMP and other standards as they relate to the design and manufacture of medical devices. Proficient
from: Olympus Corporation of the Americas - 21 days ago
Olympus Corporation of the Americas - Westborough, MA, US
interpretation of worldwide regulatory standards and laws applicable to the medical device industry e.g., ISO, QSR, GMP Knowledge of and minimum 5 years' experience in supplier quality engineering High level
from: Olympus Corporation of the Americas - More than 30 days ago
Shepherd Regulatory Search - Marlborough, MA, United States
or engineering field; electrical engineering is preferred. 10+ years of experience with development and compliance testing of Class II electro-mechanical medical devices. Knowledge of standards and regulations
from: linkedin.com - 9 days ago
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