Internal Quality Audit Medical Device Jobs
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
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
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
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
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
Register your RESUMEfrom: resume-library.com - 24 days ago
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
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
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
Register your RESUMEfrom: resume-library.com - 19 days ago
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
Register your RESUMEfrom: resume-library.com - 21 days ago
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
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