Medical Device Auditor Jobs

Terumo Medical Corporation - Elkton, MD, United States

Knowledge of national and international regulations applicable to medical devices including; Quality System Regulations, 21 CFR 820, 21CFR 803 and 804 (MDR regulations), Canadian Medical Device Regulations

from: linkedin.com - 6 days ago

Blatchford US - Miamisburg, OH, United States

in a similar role in a Medical Device environment Experience of health, safety, and environmental including OSHA. Excellent team leader Demonstrated management experience. Strong collaborator What can we offer

from: linkedin.com - 13 days ago

Boston Scientific - Arden Hills, MN, US

. Experience with or working for medical device suppliers. Demonstrated project management ability to influence cross functional global teams spanning quality, operations, R&D, and sourcing. Experience in design

from: Boston Scientific - 7 days ago

EPM Scientific - , CA, United States

IVD Lead Auditor Job type: Permanent Location: Home Based (USA) A renowned and well-established Notified Body that are committed to ensuring the safety and efficacy of medical devices are looking

from: linkedin.com - 5 days ago

Kelly Science, Engineering, Technology & Telecom - Irvine, CA, United States

Medical Devices Regulations SOR 98-282, Japan’s MHLW MO 169, EU MDR Lead Auditor certification from an accredited / recognized organization (preferred) Project management experience (preferred

from: linkedin.com - 4 days ago

Collins Consulting Inc - Westford, Massachusetts

validation exp. With IQ, OQ and PQ a must Must have a medical device background Must be able to speak and work with suppliers/vendors. Will be responsible for corrective action with suppliers/vendors Process

from: resume-library.com - 2 days ago

EPM Scientific - , NC, United States

810, 811 and 820) Strong leadership/management qualifications – at least 3 years managing direct reports Deep familiarity with medical device FDA regulatory submissions such as 510K, Letter to File

from: linkedin.com - 9 days ago

GForce Life Sciences - Minneapolis, MN, United States (+1 location)

in scientific/engineering related field. 2+ years’ experience supporting clinical quality activities/ensuring GCP compliance in GCP & FDA-regulated activities; medical devices research experience preferred

from: linkedin.com - 12 days ago

Katalyst Healthcares & Life Sciences - Carlsbad, California

techniques. Auditing experience to 21CFR820.30, 21CFR820.100, ISO13485, IS(phone number removed):2012, CMDR, the Medical Device Directive and MDSAP. Training in Risk Management, ISO 14971:2012, hazard analysis

from: resume-library.com - 6 days ago

MEDVACON TALENT ACQUISITION, LLC - Minnetonka, MN, United States

+ years relevant experience within medical device industry or related function Knowledge of GMP, ISO, QSR and other applicable international regulations, standards, Directives and Guidance Good statistical

from: linkedin.com - 17 days ago