Internal Quality Audit Medical Device Jobs in Hopkinton, MA

Stryker - Shirley, MA

Engineers to develop robust verification test strategies. Analyze failures using root cause analysis techniques. Perform supplier development activities, including PPAP. Conduct internal quality system audits

from: Dice.com - 17 days ago

Global Life Science Hub - Lexington, Massachusetts

Device Software, Hardware, and Cybersecurity. Ensure timely resolution of internal and external audit findings. Collaborate with teams to create and implement action plans for CAPA, Complaint

from: resume-library.com (+1 source) - 9 days ago

Talnt - Boston, MA, United States

requirements, and corporate standards. Assist in audit preparations and follow-ups, both internal and external, to maintain compliance standards. Participate in and drive quality system improvements

from: manatal.com - More than 30 days ago

Johnson and Johnson - Raynham, MA

actions or decisions conducted) are in compliance to standards such as the QSRs, ISO 13485, etc. • Champions compliance to applicable Global Regulations and standards (e.g. QSRs, ISO, EN and Medical Device

from: Johnson and Johnson - 5 days ago

AbbVie - Worcester, Massachusetts

for implementing and maintaining the effectiveness of the quality system for drug, biologics, device and/or combination products including compliance with Corporate policies, processes and procedures. Design

from: resume-library.com - 25 days ago

Boston Scientific - Marlborough, MA, US

problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. Supports internal and external regulatory audits. Provides technical leadership to business units

from: Boston Scientific - More than 30 days ago

Deephealth - Somerville, Massachusetts

authorities if needed. Support regulatory, customer, and internal audits. Assist in general tasks to support the maintenance and improvement of the Quality Management System PLEASE NOTE

from: resume-library.com - 17 days ago

Katalyst Healthcares & Life Sciences - Wilmington, Massachusetts

resulting from quality events, audits, or regulatory changes to ensure compliance with FDA 21 CFR 820. Assisting in the development of the company quality system to support medical device offerings

from: resume-library.com - 24 days ago

LS Solutions - Cambridge, MA

-appropriate approach for project implementation in collaboration with the vendor Medical Device Remediation Project: Implement a real risk-based approach to reduce the effort required for remediation. Guide

from: get.it - More than 30 days ago