Internal Quality Audit Medical Device Jobs

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Sr. Design Assurance Engineer (Sustaining)  

Philips - San Diego, CA, US

knowledge of current regulatory requirements, applicable laws, and standards as well as internal quality system requirements. Represent Philips as appropriate FDA, notified body, internal and external audits

from: jobvertise.com - More than 30 days ago

Associate director quality assurance information systems management  

Vertex Pharmaceuticals - Boston, Massachusetts

governing regulations such as FDA's 21 CFR Part11. Familiarity with medical device regulations to appropriately assess and validate embedded med device software applications. Preferred industry standard audit

from: snapjobsearch.com - 17 days ago

Supplier Quality Engineer  

Philips - Orlando, FL, US

quality technical skills and mindset, manufacturing process experience Project/time management skills, strong collaboration/teamwork ability Medical device experience a plus Ability to work on assignments

from: jobvertise.com - 29 days ago

Sr. Regulatory Specialist-CT/AMI  

Philips - Orange, OH, US

such as FDA, 3rd party external regulatory agencies like SFDA, KFDA, JPAL, etc. and notified body audits. Implements internal or external quality system audits. Reporting to the Director of Regulatory Affairs

from: jobvertise.com - 15 days ago

Clinical Quality Assurance Manager - Remote  

Olympus Corporation of the Americas - Center Valley, PA, US

quality assurance/operations roles (medical device industry strongly preferred). Minimum of 10 years' experience in medical device or pharmaceutical industry. Direct experience interacting with FDA

from: Olympus Corporation of the Americas - 20 days ago

Associate Director, Clinical Monitoring Oversight  

Clinical Dynamix, Inc. - Cambridge, MA, US

and review, management of clinical systems, oversight of clinical metrics tracking and reporting), inspection readiness efforts and audit-ready Trial Master Files reviews (internal and at CRO). Travel required

from: jobvertise.com - 16 days ago

Senior Quality Engineer  

Katalyst Healthcares & Life Sciences - Wilmington, Massachusetts

, bachelors degree, quality engineering, GMP, medical device, process engineering, IQ, OQ, PQ, external audit, internal audit, customer identity, QMS Nonconformance, Capa, ISO 13485,FDA,validation,audit,risk

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from: resume-library.com - 24 days ago

Validation Engineer  

Katalyst Healthcares & Life Sciences - Hopkinton, Massachusetts

regulatory inspections and internal audits. Education & Experience: Bachelor's degree (or equivalent) in engineering/science 4+ years' experience hands-on experience in Biotech, Pharmaceuticals or Medical

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from: resume-library.com - 19 days ago

Quality (QC) Inspector  

Design West Technologies, Inc. - Tustin, CA 92780, USA

environment. Requirements: High school diploma or equivalent Minimum 2-5 years' experience in quality assurance or inspection, preferably in an aerospace, defense, automotive, medical devices, or manufacturing $26 - $33 per hour

from: applicantpro.com - 22 days ago

Associate Specialist – Premarket Regulatory Affairs  

Applied Medical - Rancho Santa Margarita, California

skills and attributes: At least one year of experience in Regulatory Affairs or Quality Assurance in the medical device industry Proficient in interpreting regulations and standards Highly motivated, self

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from: resume-library.com - 21 days ago


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