Job Title: Medical Device Lead Auditor Location: Americas and the Caribbean, North America, United States (REMOTE...) Salary: £120,000.00 - £140,000.00 Per annum Job Duties: Lead and conduct audits of medical device manufacturing...
in the Quality Assurance audit and support services industry? We're looking for a Medical Device Auditor that wants to build...Medical Device Auditors - Full-time - USA remote with extensive travel. Interested in future career opportunities...
career opportunities in the Quality Assurance audit and support services industry? We're looking for a Medical Device Auditor...Job Description: Medical Device Auditors - Full-time - USA remote with extensive travel. Interested in future...
career opportunities in the Quality Assurance audit and support services industry? We're looking for a Medical Device Auditor...Job Description: Medical Device Auditors - Full-time - USA remote with extensive travel. Interested in future...
on , , , , and . Job Description Purpose The Sr. Manager, Medical Device Quality Systems, is responsible for supporting the sustainment, improvement... in both current and emerging regulations and standards impacting AbbVie medical device and combination products. Performs regulatory...
of engineering experience in the medical device industry (required). Familiarity with FDA 21 CFR 820 and ISO 13485 standards...Quality Engineer - Medical Devices We're seeking an experienced Quality Engineer to help maintain our quality system...
of engineering experience in the medical device industry (required). Familiarity with FDA 21 CFR 820 and ISO 13485 standards...Quality Engineer - Medical Devices We're seeking an experienced Quality Engineer to help maintain our quality system...
of engineering experience in the medical device industry (required). Familiarity with FDA 21 CFR 820 and ISO 13485 standards...Quality Engineer – Medical Devices We’re seeking an experienced Quality Engineer to help maintain our quality system...
of engineering experience in the medical device industry (required). Familiarity with FDA 21 CFR 820 and ISO 13485 standards...Quality Engineer - Medical Devices We're seeking an experienced Quality Engineer to help maintain our quality system...
of engineering experience in the medical device industry (required). Familiarity with FDA 21 CFR 820 and ISO 13485 standards...Quality Engineer - Medical Devices We're seeking an experienced Quality Engineer to help maintain our quality system...
of engineering experience in the medical device industry (required). Familiarity with FDA 21 CFR 820 and ISO 13485 standards...Quality Engineer - Medical Devices We're seeking an experienced Quality Engineer to help maintain our quality system...
of engineering experience in the medical device industry (required). Familiarity with FDA 21 CFR 820 and ISO 13485 standards...Quality Engineer - Medical Devices We're seeking an experienced Quality Engineer to help maintain our quality system...
The Quality Manufacturing Engineer (plastic medical device manufacturing) will oversee product quality assurance... compliance with ISO/QS standards at the Royalton, VT location. The Quality Manufacturing Engineer (Plastics Medical Device...
. Responsible for Cyber Security, Medical Device Vulnerability, Medical Device Integration, and Project Management of medical... and establish comprehensive action plans to address gaps and enable successful execution of medical device integration...
Royalton, VT location. The Quality Manufacturing Engineer (Plastics Medical Device Manufacturing) Will: Oversee quality... complaint resolution, and process quality management, with a focus on precision injection molding. They will also lead quality...
policies and procedures. As a lead auditor, leading a team of auditors, technical experts, auditors-in-training... and/or volunteer auditors provides direction and guidance to audit team. As a team auditor, works under the direction of a lead auditor...
policies and procedures. As a lead auditor, leading a team of auditors, technical experts, auditors-in-training... and/or volunteer auditors provides direction and guidance to audit team. As a team auditor, works under the direction of a lead auditor...
, biotech or medical device required. Knowledgeable in the following regulations/regulatory guidelines: 21 CFR Part 11...Job Profile Summary This Sr QA Auditor will work with IQVIAs wholly owned subsidiary and laboratory division, Q2 Lab...
, and medical device industries? We are seeking an experienced QA Compliance Consultant Auditor to join our innovative team...Job Title: GCP/GLP/GCLP Auditor and SOP Technical Writer, QA Compliance Consultant. US Job Location: Raleigh, NC, USA...
Arthrex is a global medical device company and a leader in new product development and medical education in orthopedics...Requisition ID: 62109 Title: Finance Internal Auditor I Division: Arthrex, Inc. (US01) Location: Naples, FL...