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...
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...
Our Client, a Business Manufacturing And Supply company, is looking for a Medical Device File Compliance Coordinator... of Medical Device Files (MDFs) in accordance with ISO 13485 standards. This position will also be responsible for performing...
, maintenance, and management of Medical Device Files (MDFs) in accordance with ISO 13485 standards. This position..., and updating medical device files in accordance with ISO 13485. Coordinating across functions (development, operations...
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...
to lead nationally in innovating equitable whole-person health. The role of Auditor, Payment Integrity will identify claim... audit review methods and practices, including but not limited to; claim payment evaluation, medical chart review, claim...
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...
Lead Auditor Certification strongly preferred Experience conducting internal audits in accordance with ISO 13485 and/or 21... CFR Part 820 in a medical device setting strongly preferred REQUIRED SKILLS & ABILITIES Strong familiarity with ISO...