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102 results (4 new)

Group by company

Quality Engineer

Exarca Inc.

Hybrid in Phoenix, Arizona • Yesterday

Easy Apply

Contract

Depends on Experience

Senior QA Engineer

ChaTeck Incorporated

Hybrid in Phoenix, Arizona • 17d ago

Easy Apply

Contract, Third Party

Depends on Experience

Staff Product Quality Engineer

ON Semiconductor

Scottsdale, Arizona • Today

Full-time

Advanced Manufacturing Quality Engineer

Johnson Controls

Gilbert, Arizona • Today

Full-time

Quality Engineer

Motion Recruitment Partners, LLC

Remote or Irvine, California • Today

Easy Apply

Contract

QA Engineer

Infinite Computer Solutions (ICS)

Remote • 24d ago

Easy Apply

Full-time

60,000 - 80,000

QA ENGINEER

AaraTechnologies Inc

Remote or Hybrid in California City, California • 8d ago

Easy Apply

Contract

$65,000 - $75,000

QA ENGINEER

AaraTechnologies Inc

Remote or Hybrid in Virginia Beach, Virginia • 9d ago

Easy Apply

Contract

$65,000 - $75,000

Engineer I, Quality

LG Energy Solution Michigan, Inc.

Phoenix, Arizona • Today

Full-time

Mechanical Quality and Commissioning Engineer

LotusWorks

Chandler, Arizona • Today

Full-time

AI Quality Engineer

Innoworx Technology Services LLC

Remote • Today

Easy Apply

Contract

Depends on Experience

Data Quality Engineer

Kforce Technology Staffing

Remote or Davie, Florida • Today

Contract, Third Party

$50 - $75 hourly

SAP Quality Engineer - Remote

The Dignify Solutions, LLC

Remote • Today

Easy Apply

Contract, Third Party

$65

Product & Process Quality Engineer (Remote)(No H-1B or Corp to Corp)

NetSource, Inc.

Remote • Today

Easy Apply

Contract

Depends on Experience

Senior Product Quality Assurance Engineer (I&G)

ResMed Corporation

Remote • Today

Full-time

USD 122,000.00 - 184,000.00 per year

Lead Software Quality Assurance Engineer

Wabtec

Remote or Kansas City, Missouri • Today

Full-time

USD 68,900.00 - 98,200.00 per year

Quality Engineer/SDET - Nexa

Widescope Consulting and Contracting Services

Remote • 18d ago

Easy Apply

Full-time

80,000 - 110,000

HCM Test Automation & Quality Engineer

CACI International, Inc.

Remote • Today

Full-time

USD 90,300.00 - 189,600.00 per year

Substation Structural Training & Quality Engineer

Ulteig

Remote • Today

Full-time

USD 123,200.00 - 159,650.00 per year

Lead SDET / Automation Engineer

The Jupiter Group

Remote • 21d ago

Easy Apply

Contract

Depends on Experience

Software Quality Assurance Manager 2

Northrop Grumman

Remote or Los Angeles, California • Today

Full-time

USD 146,600.00 - 219,800.00 per year

Software QA Engineer L4

Frontdoor, Inc.

Remote • Today

Full-time

USD 103,000.00 - 120,000.00 per year

Sr. Engineer, Supplier Quality (Remote)

Getinge Castle

Remote or Lansing, Michigan • Today

Full-time

USD 96,240.00 - 120,300.00 per year

Software QA Engineer 2

Dexcom

Remote or San Diego, California • Today

Full-time

USD 78,900.00 - 131,500.00 per year

Quality Assurance Analyst

Randstad Digital

Remote or Beaverton, Oregon • Today

Contract

USD24 - USD35

Sr Machine Learning Engineering Manager - AI Quality and Governance

Workiva

Remote • Today

Full-time

USD 193,000.00 - 308,000.00 per year

Aerospace Quality Engineer / MRB Engineer / Manufacturing Quality Engineer MRB, RCCA & Composite Manufacturing

Nityo Infotech Corporation

Remote • 10d ago

Easy Apply

Full-time

$80,000 - $100,000

Lead Engineer Automation Quality

Empower Annuity Insurance Company of America

Remote or Overland Park, Kansas • 17d ago

Full-time

USD 105,700.00 - 149,275.00 per year

Principal Software Engineer, Intelligent Quality Solutions

Humana Inc

Remote • 25d ago

Full-time

USD 156,600.00 - 215,400.00 per year

Design Quality Engineer- Medical Devices

Synkriom

Remote • Yesterday

Easy Apply

Contract

$30 - $40

Job Details

Skills

medical device
Quality Engineer

Summary

Quality Engineer

Phoenix, AZ

We are seeking a Quality Engineer to support quality and compliance activities within pharmaceutical, biotechnology, and medical device manufacturing environments. The Quality Engineer will work with cross-functional teams to identify quality issues, investigate root causes, implement corrective actions, and support continuous improvement initiatives.

Key Responsibilities

Support quality assurance and quality control activities in manufacturing environments.
Investigate deviations, nonconformances, and quality issues.
Lead or support Root Cause Analysis (RCA) and CAPA activities.
Support Change Control and document change-related quality impacts.
Review and maintain quality documentation, procedures, and records.
Analyze quality and manufacturing data to identify trends and recurring issues.
Support process and product improvement initiatives.
Participate in internal and external audits and inspections.
Work with Manufacturing, Engineering, Validation, and Regulatory teams to resolve quality issues.
Ensure manufacturing and quality activities comply with applicable GMP, FDA, ISO, and company requirements.
Support supplier quality activities, investigations, and supplier-related corrective actions when required.
Assist with risk assessments and implementation of appropriate risk mitigation actions.
Prepare quality reports, investigation summaries, and other technical documentation.

Required Qualifications

Bachelor’s degree in Quality Engineering, Mechanical Engineering, Industrial Engineering, Biomedical Engineering, Chemical Engineering, or a related field.
Experience in Quality Engineering, Quality Assurance, Manufacturing, or a related role.
Experience working in a Pharmaceutical, Biotech, Medical Device, or other regulated manufacturing environment.
Knowledge of GMP, FDA regulations, and/or ISO quality standards.
Experience with CAPA, deviations/nonconformances, Root Cause Analysis, and Change Control.

Preferred Qualifications

Experience with medical device quality systems and ISO 13485.
Knowledge of ISO 14971 and risk management.
Experience with FDA 21 CFR Part 820/QMSR requirements.
Experience with pharmaceutical GMP and 21 CFR Part 210/211.
Familiarity with Lean Manufacturing, Six Sigma, or Continuous Improvement methodologies.
Experience with validation, process improvement, or manufacturing engineering.
Experience supporting FDA or other regulatory inspections.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91118102
Position Id: 9101182
Posted 1 day ago

Fitment

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Contact the job poster

Santosh Sharma

Recruiter @ Exarca Inc.

View Profile

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Job Details

Skills

medical device
Quality Engineer

Summary

Quality Engineer

Phoenix, AZ

Key Responsibilities

Support quality assurance and quality control activities in manufacturing environments.
Investigate deviations, nonconformances, and quality issues.
Lead or support Root Cause Analysis (RCA) and CAPA activities.
Support Change Control and document change-related quality impacts.
Review and maintain quality documentation, procedures, and records.
Analyze quality and manufacturing data to identify trends and recurring issues.
Support process and product improvement initiatives.
Participate in internal and external audits and inspections.
Work with Manufacturing, Engineering, Validation, and Regulatory teams to resolve quality issues.
Ensure manufacturing and quality activities comply with applicable GMP, FDA, ISO, and company requirements.
Support supplier quality activities, investigations, and supplier-related corrective actions when required.
Assist with risk assessments and implementation of appropriate risk mitigation actions.
Prepare quality reports, investigation summaries, and other technical documentation.

Required Qualifications

Bachelor’s degree in Quality Engineering, Mechanical Engineering, Industrial Engineering, Biomedical Engineering, Chemical Engineering, or a related field.
Experience in Quality Engineering, Quality Assurance, Manufacturing, or a related role.
Experience working in a Pharmaceutical, Biotech, Medical Device, or other regulated manufacturing environment.
Knowledge of GMP, FDA regulations, and/or ISO quality standards.
Experience with CAPA, deviations/nonconformances, Root Cause Analysis, and Change Control.

Preferred Qualifications

Experience with medical device quality systems and ISO 13485.
Knowledge of ISO 14971 and risk management.
Experience with FDA 21 CFR Part 820/QMSR requirements.
Experience with pharmaceutical GMP and 21 CFR Part 210/211.
Familiarity with Lean Manufacturing, Six Sigma, or Continuous Improvement methodologies.
Experience with validation, process improvement, or manufacturing engineering.
Experience supporting FDA or other regulatory inspections.

Dice Id: 91118102
Position Id: 9101182
Posted 1 day ago

Fitment

Dice Job Match Score™

To see how well you match this job, please log in or create an account.

Once logged in, be sure to complete your profile to get the most accurate match score.

Contact the job poster

Santosh Sharma

Recruiter @ Exarca Inc.

View Profile

Create job alert

Never miss an opportunity! Create an alert based on the job you applied for.

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