Medical Device Audit Senior Jobs

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 - 6 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 - Yesterday

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 - 3 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 - 6 days ago

Lowell Inc. - Brooklyn Park, MN, United States

for the development and production of technologically advanced, implantable medical devices for the cardiovascular, spine, trauma and extremities markets. We manufacture components and assemblies that save lives

from: linkedin.com - 5 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 - 2 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 - 12 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

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 - 27 days ago

Philips - Orange, OH, US

if: Youve acquired a minimum of 7 years' Regulatory Affairs experience within FDA regulated, complex Medical Device/Software (SiMD/SaMD) environments, including leadership/guidance on global regulatory

from: jobvertise.com - More than 30 days ago