Internal Quality Audit Medical Device Jobs

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Principal Quality Engineer  

Mayo Clinic - Rochester, Minnesota, USA

and validation • Process control and process validation in the medical device field • Leading internal audits • Test management methodologies and tools • Administration and maintenance of quality records

from: Ivyexec.com - 13 days ago

Sr Director Quality Assurance Operations  

Insmed Incorporated - Bridgewater, New Jersey

for medical device products and combination products. Lead the quality assessment for product lifecycle changes, efficiency projects, and continuous improvement projects. Manage the performance and development

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from: resume-library.com - 27 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 - 14 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 - 4 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

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from: resume-library.com (+1 source) - 2 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

Design Controls Manager  

Abbott Laboratories - Bend, Oregon

, industrial, or quality engineering. Minimum 10 years of Medical device development and/or other highly regulated industry. In-depth knowledge of the Quality System Regulation (QSR), ISO 13485, MDSAP, and EU

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from: resume-library.com - 3 days ago

Staff Software Quality Engineer  

Abbott Laboratories - Westford, Massachusetts

initiatives that measurably enhance medical device software and cybersecurity lifecycle activities Lead Product/Process improvement efforts by identifying methods to capture quality metric data

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from: resume-library.com - 2 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 - 6 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) - 20 days ago


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