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 - 8 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 - 14 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 - 11 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 - 6 days ago
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 - 8 days ago
Hamilton Medical, Inc. - Reno, Nevada
changes. Conducts and documents internal non-conformance and customer complaint investigations. Support in Medical Device reporting (MDRs), complaints, field corrective action (Recall) and management review
Register your RESUMEfrom: resume-library.com - 3 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 - 5 days ago
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 - 5 days ago
ICONMA, LLC - Des Plaines, Illinois
or equivalent combination of experience and education. At least one year in quality assurance role in medical device industry is preferred. As an equal opportunity employer, ICONMA provides an employment
Register your RESUMEfrom: resume-library.com - 3 days ago
VRS Recruitment (US) - Huntington, NY, United States
recruiter, Mass Spec recruiter, Chromatography recruiter, quality assurance, internal audit, ISO, ISO 9001, ISO 13485, ISO 14001, ISO 27001, return service, regulatory compliance, QA manager, QA testing
from: linkedin.com - 7 days ago
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