Internal Quality Audit Medical Device Jobs

Avails Medical, Inc. - Menlo Park, CA, United States

Quality Management System. Support internal and supplier audits and external regulatory inspections. Become an expert in the use and maintenance of the eQMS. Lead the NC/CAPA documentation and investigation

from: linkedin.com - 8 days ago

Johnson and Johnson - Cincinnati, OH

, responsible for leading product quality and reliability while ensuring the implementation of ground-breaking technology for medical devices is safe, effective, and follows applicable regulations, standards

from: Johnson and Johnson - 2 days ago

Lumicity - Lowell, MA, United States

Please apply or send your resume to klelix.hamlin@lumicity.io The Quality Engineer is responsible for overseeing the quality assurance of medical devices, from initial design through manufacturing

from: linkedin.com - 5 days ago

Lumicity - Minneapolis, MN, United States

). This is a great opportunity with a company that prioritizes career-growth and has an exciting future within the Medical Device Industry. Responsibilities: Participate in internal and customer audits Lead projects

from: linkedin.com - 8 days ago

Medcura - Riverdale, MD

functional teams to execute direction for the company’s Quality compliance requirements on new and existing devices. This position is responsible for the day-to-day execution of all Quality System requirements

from: workable.com - 7 days ago

10XBeta Venture Studio - New York, NY, United States

Position Overview Join our dynamic startup team as a Quality Assurance Engineer, where you will play a crucial role in ensuring the quality and reliability of groundbreaking medical devices

from: linkedin.com - 8 days ago

TekWissen ® - Fremont, CA, United States

on field data as required Provide input, feedback, and data for Quality report outs, Management Review, etc. Support internal and external audits (FDA, ISO, MDSAP, etc.) Minimum Requirements/Qualifications

from: linkedin.com - 8 days ago

Midas Management and Research - Irwindale, California

+ years) in quality assurance within medical device manufacturing, with a strong understanding of FDA regulations and ISO 13485 standards. Proven experience in leading quality improvement initiatives

from: resume-library.com - 11 days ago

AOA Dx - , CO, United States

. Quality Management experience in medical devices and diagnostics. Strong computer skills, including proficiency in Microsoft Office suite applications and basic proficiency in Adobe Acrobat. Ability

from: linkedin.com - 11 days ago

EPM Scientific - New York, NY, United States

all site Quality regulatory compliance activities, play a pivotal role in maintaining the effectiveness of the Quality Management System (QMS), and ensure the effectiveness of internal and external audit

from: linkedin.com - 11 days ago