Internal Quality Audit Medical Device Jobs in Massachusetts

ACE Partners - , MA, United States

ISO 13485 compliance. Responsibilities: Support New Product Development from a Quality perspective Responsible for internal and external audits Experience in R&D Engineering, Manufacturing

from: linkedin.com - 16 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 - More than 30 days ago

EPM Scientific - Billerica, MA, United States

readiness for both internal and external audits Qualifications: Bachelors degree with approx. 8-10 years of Quality experience in medical device, combination product experience preferred Direct experience

from: linkedin.com - 21 days ago

ACE Partners - , MA, United States

to Product Quality Complaints or Inquiries Oversight of Supplier/Vendor Management Programme Manage QMS (Trackwise) Review and approve SOPs related to Medical Device and assoc systems You Need: Bachelor's

from: linkedin.com - 23 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

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

Johnson and Johnson - Danvers, MA

devices, aerospace). Risk Management: Identify and mitigate quality and supply chain risks associated with supplier activities. Collaboration: Work closely with internal departments such as procurement

from: Johnson and Johnson - 8 days ago

Johnson and Johnson - Danvers, MA

in regulated industries (e.g., medical devices, aerospace). * Risk Management: Identify and mitigate quality and supply chain risks associated with supplier activities. * Cross-functional Collaboration: Work

from: Johnson and Johnson - 8 days ago

Johnson & Johnson - Danvers, MA

and/or writing, medical device experience preferred. 5+ years of technical documentation or quality engineering experience Ability to communicate ideas and information clearly, effectively, and frequently (oral

from: Dice.com - 14 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