Internal Quality Audit Medical Device Jobs

Merz Aesthetics - Racine, Wisconsin

of quality activities related to risk. InspectionsSupport/Lead with federal, state, and local regulatory officials during regulatory inspections.Support/Lead in internal and vendor quality system audits

from: snapjobsearch.com - 7 days ago

SHL Medical - , SC, United States

documentation package Conducts internal and supports external audits as assigned to ensure compliance to company quality systems requirements. Additional Responsibilities may Include: Support Material Review

from: linkedin.com - 7 days ago

10XBeta Venture Studio - New York, NY, United States

Position Overview Join our dynamic startup team as a Quality Assurance Engineer, where you will play a crucial role in ensuring the quality and reliability of groundbreaking medical devices

from: linkedin.com - 23 days ago

Oxenham Group LLC - Mansfield, Massachusetts

Position: Quality Systems Manager Location: Onsite in Mansfield, MA Responsibilities: Oversee compliance and the quality system including doc control, complaints, CAPA, NCMR, internal audit etc

from: resume-library.com - 13 days ago

Medcura, Inc. - Riverdale, MD, United States (+1 location)

functional teams to execute direction for the company's Quality compliance requirements on new and existing devices. This position is responsible for the day-to-day execution of all Quality System requirements

from: linkedin.com (+1 source) - 5 days ago

C2Dx, Inc. - Schoolcraft, MI, United States

Audit, Internal Audit, CAPA, Nonconforming Product Procedure, Customer Feedback and Complaints, Vigilance, and duties as required by Management Contribute towards process improvements to the C2Dx Quality

from: linkedin.com - 5 days ago

TopTalentFetch - Hayward, CA, US

/External Quality Audit activities and other key quality initiatives, as appropriate Administers and maintains Quality System records Minimum Qualifications 1-3 years of experience in medical device Quality

from: jobvertise.com - 13 days ago

Brunel - , MA, United States

, exceptional attention to detail, and a deep understanding of regulatory requirements in the medical device industry. Key Responsibilities: Develop and maintain the company's quality management system (QMS

from: linkedin.com - 9 days ago

EPM Scientific - Minneapolis, MN, United States

and external audits Experience: 5-7 years of relevant experience within the medical device industry or related function Lead auditor certification preferred Background in manufacturing processes for sterile

from: linkedin.com - 12 days ago

Merz North America, Inc - Racine, WI

product risk file review; management and preparation of event-based reviews; review and coordination of quality activities related to pFMEA risk matrices. Supports Internal and Vendor Audit Functions

from: Merz North America, Inc - 9 days ago