Internal Quality Audit Medical Device Jobs

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Quality Engineer I - rms  

rms Company - Minneapolis, Minnesota (+1 location)

with an inclusive approach. Support internal and external audit activities, ensuring inclusivity and diversity are considered in all quality-related processes. Lead and participate in company projects, providing

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from: resume-library.com - 17 days ago

Manager, Analytical Quality Lab  

Merz North America, Inc - Racine, WI

Assurance: * Perform internal and vendor quality system audits. * Perform routine walk-throughs and compliance checks to verify adherence to quality guidelines. Interact with inspectors in regulatory audits

from: Merz North America, Inc - 4 days ago

Supervisor, Quality Operations  

pennsylvania

and processes. Job Qualifications Required: : Minimum of 5 years of quality operations experience within medical device manufacturing, service or distribution environment, with strong concentration in compliance Competitive

from: Tiptopjob.com - 22 days ago

Sr. Quality Systems Specialist  

Katalyst Healthcares & Life Sciences - Carlsbad, California

regulations, agency guidelines and internal policies to assure compliance. Lead process improvement projects and assessment of quality plans. Support Management during external/internal inspections

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from: resume-library.com - 7 days ago

Quality Control Lead  

Totowa, NJ

in internal audits for compliance with SOPs, GMPs, and regulations. Participates actively in technology transfer, method qualification and validation. Perform all additional Quality Control tasks as required

from: workable.com - More than 30 days ago

Quality Manager  

MSK Precision Products, Inc - Fort Lauderdale, FL 33312, USA

to the quality system and for coordinating corrective action for changes and improvements. Job Requirements: BS degree in Engineering a plus. 3 to 5 + years' experience with medical device or similar manufacturing

from: applicantpro.com - 17 days ago

Sr. GCP QA Auditor - Remote  

Medpace, Inc. - Irving, Texas (+1 location)

and medical devices. Develop audit management plans and audit strategy with clients for ongoing clinical trials. Coordinate and conduct internal system audits and external investigative site/vendor audits

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from: resume-library.com - 9 days ago

Senior Supplier Quality Engineer  

Johnson and Johnson - Danvers, MA

devices, aerospace). Risk Management: Identify and mitigate quality and supply chain risks associated with supplier activities. Collaboration: Work closely with internal departments such as procurement

from: Johnson and Johnson - 9 days ago

Quality Manager  

CorDx - Atlanta, Georgia

device manufacturing sector, with a strong background in quality management systems, regulatory compliance, and ISO standards. The Quality Manager will play a critical role in implementing, managing

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from: resume-library.com (+1 source) - 23 days ago

Senior Quality Engineer  

Johnson & Johnson - Jacksonville, Florida

, ISO 13485, etc.Champions compliance to applicable Global Regulations and standards (e.g. QSRs, ISO, EN and Medical Device Directive (MDD) requirements) including providing support during internal

from: snapjobsearch.com - 5 days ago


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