6 results (3 new)

Group by company

Purple Drive Technologies LLC

Irving, Texas • Today

Easy Apply

Full-time, Part-time, Third Party, Contract

LCM Quality Engineer | Medical Devices

Galaxy i Technologies, Inc.

Irving, Texas • Today

Third Party, Contract

Depends on Experience

Field Service Engineer II (Medical Devices) - Dallas, TX

Boston Scientific Corporation

Dallas, Texas • Today

Full-time

USD 55,432.00 - 94,224.00 per year

Quality Inspector

Motion Recruitment Partners, LLC

Remote or Downers Grove, Illinois • Today

Easy Apply

Contract

Compensation information provided in the description

Windchill Solution Architect/Senior Windchill PLM Consultant Medical Device Industry

EdgeAll

Remote • Today

Easy Apply

Contract, Third Party

80 - 90

Medical Device V&V engineers

Katalyst Healthcares and Lifesciences

Remote or New Jersey • 19d ago

Full-time

Job Details

Skills

Technology Transfer
QMS
IQ
OQ
PQ
Quality Audit
Risk Assessment
Continuous Improvement
Issue Resolution
Collaboration
Research and Development
Regulatory Affairs
Regulatory Compliance
Management
LCM
Quality Assurance
Design Controls
Verification And Validation
Risk Management
FMEA
Corrective And Preventive Action
Root Cause Analysis
Change Control
Systems Analysis
Documentation
Analytical Skill
Problem Solving
Conflict Resolution
Communication
Product Development
Manufacturing
Quality Management
Medical Devices

Technology Transfer
QMS
IQ
OQ
PQ
Quality Audit
Risk Assessment
Continuous Improvement
Issue Resolution
Collaboration
Research and Development
Regulatory Affairs
Regulatory Compliance
Management
LCM
Quality Assurance
Design Controls
Verification And Validation
Risk Management
FMEA
Corrective And Preventive Action
Root Cause Analysis
Change Control
Systems Analysis
Documentation
Analytical Skill
Problem Solving
Conflict Resolution
Communication
Product Development
Manufacturing
Quality Management
Medical Devices

Summary

Job Description: LCM Quality Engineer - Medical Devices

Job Summary

The LCM (Life Cycle Management) Quality Engineer will provide quality engineering support for medical device products throughout product development, design changes, technology transfer, manufacturing transfer, and sustaining engineering activities. The role ensures compliance with the Quality Management System (QMS), applicable regulatory requirements, and internal quality standards.

Key Responsibilities

Provide quality engineering support for new product development (NPD), design changes, product transfers, and sustaining engineering activities.
Develop and maintain Quality Plans and Product Development Process documentation.
Review and approve verification and validation (V&V) protocols, reports, and related documentation.
Support the preparation and review of DFMEA and PFMEA documentation.
Support equipment and process qualification activities, including IQ, OQ, and PQ.
Participate in quality audits, risk assessments, and continuous improvement initiatives.
Lead or support root cause analysis (RCA), nonconformance investigations, deviations, and Corrective and Preventive Actions (CAPA).
Review and manage engineering change orders and product/process change control documentation.
Apply statistical methods, process capability analysis, and measurement system assessments to evaluate product and process quality.
Support post-market quality activities, including complaint investigations and quality issue resolution.
Develop, review, and maintain SOPs, work instructions, and other quality documentation.
Collaborate with R&D, Manufacturing, Regulatory Affairs, and other cross-functional teams to ensure product quality and regulatory compliance.

Required Skills and Qualifications

Experience in Life Cycle Management (LCM) Quality Engineering, preferably within the medical device industry.
Knowledge of medical device regulations and Quality Management Systems.
Experience with NPD processes, design controls, and sustaining engineering.
Understanding of verification and validation, risk management, DFMEA/PFMEA, and process validation.
Experience with nonconformances, deviations, CAPA, root cause analysis, and change control.
Familiarity with statistical methods, process capability, and measurement system analysis.
Strong documentation, analytical, problem-solving, and cross-functional communication skills.

Preferred Experience

Experience supporting medical device product development, manufacturing transfers, and post-market quality activities.
Familiarity with regulated quality systems and applicable medical device standards.

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: 91018020
Position Id: PDT - 12185-13320-1793125648
Posted 8 hours ago

Company Info

About Purple Drive Technologies LLC

Founded in 2007, Purple Drive started as a tech solutions firm and has grown into a full-service consulting and talent partner. We help businesses navigate complex technology challenges while connecting top professionals with career-defining opportunities.

We believe in transforming businesses through smart IT solutions and empowering technologists to grow their expertise through challenging projects and meaningful partnerships. Built on over 20 years of trusted relationships, we create success stories for both our clients and the talented professionals who drive innovation forward.

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.

Create job alert

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

Milpitas, California

•

Today

Senior Verification & Validation (V&V) Engineer - Medical Devices Industry: Medical Devices Key Skills: Verification & Validation (V&V), Protocol Development, Test Execution, Validation Reporting, ISO 13485, FDA Regulations, IEC 62304 Job Summary We are seeking a Senior Verification & Validation (V&V) Engineer with medical device industry experience to develop, execute, and document verification and validation protocols in a regulated environment. The ideal candidate will have strong IT system

Easy Apply

Full-time, Part-time, Third Party, Contract

Job Details

Skills

Technology Transfer
QMS
IQ
OQ
PQ
Quality Audit
Risk Assessment
Continuous Improvement
Issue Resolution
Collaboration
Research and Development
Regulatory Affairs
Regulatory Compliance
Management
LCM
Quality Assurance
Design Controls
Verification And Validation
Risk Management
FMEA
Corrective And Preventive Action
Root Cause Analysis
Change Control
Systems Analysis
Documentation
Analytical Skill
Problem Solving
Conflict Resolution
Communication
Product Development
Manufacturing
Quality Management
Medical Devices

Technology Transfer
QMS
IQ
OQ
PQ
Quality Audit
Risk Assessment
Continuous Improvement
Issue Resolution
Collaboration
Research and Development
Regulatory Affairs
Regulatory Compliance
Management
LCM
Quality Assurance
Design Controls
Verification And Validation
Risk Management
FMEA
Corrective And Preventive Action
Root Cause Analysis
Change Control
Systems Analysis
Documentation
Analytical Skill
Problem Solving
Conflict Resolution
Communication
Product Development
Manufacturing
Quality Management
Medical Devices

Summary

Job Description: LCM Quality Engineer - Medical Devices

Job Summary

Key Responsibilities

Provide quality engineering support for new product development (NPD), design changes, product transfers, and sustaining engineering activities.
Develop and maintain Quality Plans and Product Development Process documentation.
Review and approve verification and validation (V&V) protocols, reports, and related documentation.
Support the preparation and review of DFMEA and PFMEA documentation.
Support equipment and process qualification activities, including IQ, OQ, and PQ.
Participate in quality audits, risk assessments, and continuous improvement initiatives.
Lead or support root cause analysis (RCA), nonconformance investigations, deviations, and Corrective and Preventive Actions (CAPA).
Review and manage engineering change orders and product/process change control documentation.
Apply statistical methods, process capability analysis, and measurement system assessments to evaluate product and process quality.
Support post-market quality activities, including complaint investigations and quality issue resolution.
Develop, review, and maintain SOPs, work instructions, and other quality documentation.
Collaborate with R&D, Manufacturing, Regulatory Affairs, and other cross-functional teams to ensure product quality and regulatory compliance.

Required Skills and Qualifications

Experience in Life Cycle Management (LCM) Quality Engineering, preferably within the medical device industry.
Knowledge of medical device regulations and Quality Management Systems.
Experience with NPD processes, design controls, and sustaining engineering.
Understanding of verification and validation, risk management, DFMEA/PFMEA, and process validation.
Experience with nonconformances, deviations, CAPA, root cause analysis, and change control.
Familiarity with statistical methods, process capability, and measurement system analysis.
Strong documentation, analytical, problem-solving, and cross-functional communication skills.

Preferred Experience

Experience supporting medical device product development, manufacturing transfers, and post-market quality activities.
Familiarity with regulated quality systems and applicable medical device standards.

Dice Id: 91018020
Position Id: PDT - 12185-13320-1793125648
Posted 8 hours ago

Company Info

About Purple Drive Technologies LLC

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.

Create job alert

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

Milpitas, California

•

Today

Easy Apply

Full-time, Part-time, Third Party, Contract

LCM Quality Engineer Medical Devices

Skills

Summary

Job Description: LCM Quality Engineer - Medical Devices

Job Summary

Key Responsibilities

Required Skills and Qualifications

Preferred Experience

Dice Job Match Score™

Similar Jobs

LCM Quality Engineer Medical Devices

Job Details

Skills

Summary

Job Description: LCM Quality Engineer - Medical Devices

Job Summary

Key Responsibilities

Required Skills and Qualifications

Preferred Experience

Company Info

About Purple Drive Technologies LLC

Dice Job Match Score™

Similar Jobs