Medical Device Audit Senior Jobs

X4 Life Sciences - New York, NY, United States

and regulatory compliance of QMS medical devices. This position involves a range of responsibilities, including managing deviations, conducting internal audits, addressing nonconformities, implementing corrective

from: linkedin.com - 4 days ago

Instrument Technology, Inc. - Westfield, MA, United States

System (QMS). As the Senior Design & Quality Engineer you will lead and maintain our ISO 13485 certification, through audits, training, and other applicable compliance tasks. You will hold yourself

from: linkedin.com - 13 days ago

Varian Medical Systems - Austin, Texas

preferred. 10-15 years of medical device experience. Minimum of 7 years management experience. Ability, competence, and confidence to lead people. Effective interpersonal skills. Experience with Class II

from: resume-library.com - 3 days ago

Facet Medical Technologies LLC - East Point, GA, United States

13485, CFR 820, and EU MDD/MDR regulations. Proficiency in process improvement methodologies, Statistical Process Control (SPC), and other statistical process methods is essential. Experience in medical

from: linkedin.com - 10 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 - 18 days ago

Abbott Laboratories - Plymouth, Minnesota

of personnel, tooling, and equipment in assigned areas. Assemble, bond, coat, and process medical devices and related parts using microscopes and applicable tools. Assists in providing direct training to area

from: resume-library.com - 7 days ago

Triton Medical Robotics - Burlingame, CA, United States

quality by maintaining compliance, reviewing device complaints, reviewing audit reports and implementing corrective actions. Regularly communicates study status to senior management and represents

from: linkedin.com - 18 days ago

Device Search Group - , CA, United States

by regulatory bodies. If you have a proven track record in the medical device industry, enjoy working with small organizations and a passion for continuous improvement, we want to hear from you. Key

from: linkedin.com - 24 days ago

GSK - Durham, NC

supporting GxP activities. Entity external audits 3rd Party Service Suppliers Software as a Medical Device (SaMD) audits. For Cause audits based on identified risks or regulatory actions Progress audits

from: Pharmadiversityjobboard.com - 11 days ago

Cordis - Irvine, California

/Biomedical/Pharmacy or equivalent professional experience. • 2+ years of experience in regulatory affairs in medical device/pharmaceutical industry, GLP, ISO 13485 environment • Experience in FDA / EU

from: resume-library.com - 15 days ago