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Manufacturing Engineer

Q1 Technologies, Inc.

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Salt Lake City, Utah, USA

Full-time

Manufacturing Engineer Salt Lake City, UT Job Description: 5+ years of experience & demonstrated proficiency in manufacturing, Process validation & providing ongoing technical support is preferred with evidence of continued self-development. Work experience in the Medical Device industry. Must Have Technical/Functional Skills In-depth knowledge of FDA regulations, Industry standards, and guidelines such as ISO 13485 and ISO 14644. Experience in control facility, warehouse and cleanroom validati
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Posted 60+ days ago | Updated 4 hours ago

Regulatory Affairs Specialist

IKCON TECHNOLOGIES Inc.

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New Jersey, USA

Contract, Third Party

IKCON TECHNOLOGIES INC delivers exceptional IT services and solutions that provide clients with definite edge over competitors and promoting highest standards of quality. We are currently looking for a Regulatory Affairs Specialist with one of our clients in Remote, Remote. If you are actively looking for opportunities, please send us your updated resume with your contact details. JOB TITLE Regulatory Affairs Specialist/Senior Specialist for Drug-Device Combination Products CITY Remote STATE
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Posted 60+ days ago | Updated 2 days ago

Systems Engineer

Philips North America

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New Kensington, Pennsylvania, USA

Full-time

Job Title Systems Engineer Job Description The Systems Engineer will play a critical role as a part of the Sleep and Respiratory Care R&D/Systems Engineering Team that is responsible for developing and sustaining respiratory ventilators and sleep therapy devices, ensuring our Sleep & Respiratory Care (S&RC) products are safe, reliable and of the highest quality. Your role: Lead systems engineering activities including requirements translation, system architecture development, and subsystem in
Posted 57 days ago | Updated 11 hours ago