Internal Quality Audit Medical Device Jobs

Skills Alliance - , MA, United States

’ experience in Quality Assurance, Quality Engineering or related functions in a medical device or other FDA regulated company. Prefer degree in Engineering, Science or related field. Develop, implement

from: linkedin.com - 6 days ago

Proclinical Staffing - Cambridge, MA, United States

and international regulations Support internal and external audits and contribute to inspection readiness upon request Support management of deviations and risks to evaluate potential impacts on quality and determine

from: linkedin.com - 12 days ago

Boston Scientific - Marlborough, MA, US

, NCEP’s, CAPA’s PIRs, Field Signals Evaluations and Field Actions. Support internal and external regulatory audits as required. Support collection and analysis of key quality trending information and data

from: Boston Scientific - 9 days ago

BostonGene - Waltham, MA, United States

, deviation management, audit program, etc. ● Other duties as assigned. Qualifications ● BS Degree in the Sciences or other technical discipline, or 5+ years of QA experience in the medical device or diagnostic

from: linkedin.com - 4 days ago

Eliassen Group - Marlborough, MA, United States

and maintaining the quality management system, including corrective and preventive actions, calibration, preventive maintenance, and internal and external quality audits. MUST HAVES - QUALIFICATION SUMMARY

from: linkedin.com - 3 days ago

Olympus Corporation of the Americas - Westborough, Massachusetts

. Support and participate in internal and external Quality Audits (including notified bodies and health authorities) and ensure related corrective action activities are completed in a robust and timely manner

from: resume-library.com (+1 source) - Yesterday

Lowell Inc. - Brooklyn Park, MN, United States

, and lead a team of quality engineers to ensure compliance with ISO13485:2016, FDA CFR Title 21 Section 820, and other relevant standards and regulations for the medical devices. Lowell is the premier partner

from: linkedin.com - 3 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 - 4 days ago

Philips - San Diego, California

knowledge of current regulatory requirements, applicable laws, and standards as well as internal quality system requirements. Represent Philips as appropriate FDA, notified body, internal and external audits

from: resume-library.com (+1 source) - Yesterday

ACE Partners - , NJ, United States

accuracy and traceability. Quality Audits: Assist in conducting internal audits and assessments to identify areas for improvement and ensure adherence to quality standards and regulatory requirements

from: linkedin.com - 6 days ago