Top 11 Quality assurance manager Jobs in Richland Wa

Quality Engineering Manager
GT Medical Technologies, Inc. —Richland, WA
- $115,000 - $135,000 a year
- Weekends as needed
- Background check
- Engineering
- Pass drug screening
Quick Apply
Team Leader Quality
Lamb Weston —Pasco, WA
- $78,520 - $117,790 a year
- Full-time
- Ability to walk for extended periods
- Computer literacy
- Bachelor of Science
- Health savings account
- Employee stock purchase plan
4d
QA/QC Manager
McKinstry —Pasco, WA
- $89,010 - $151,300 a year
- Management
- Construction site
- US work authorization
- Profit sharing
- Commuter assistance
Enterprise Quality Assurance Manager/Team Leader
GESA CREDIT UNION —Richland, WA
- $97,069.57 - $183,843.88 a year
- Full-time
- Background check
- Computer Science
- 3 years
- Commuter assistance
- Paid holidays
Food Safety Quality Assurance & Production Lead
Local Bounti —Pasco, WA
- $28 - $30 an hour
- English
- Mid-level
- 3 years
- Paid parental leave
- Health savings account
Quick Apply
Project Manager - Air Quality
SWCA Environmental Consultants —United States
- $102,047.40 - $134,152.20 a year
- Online Application
- Remote
- 7 years
- Bachelor of Science
- Engineering
- Profit sharing
- Health insurance

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Team Leader Quality
Lamb Weston —Pasco, WA
As a quality assurance professional, he or she is involved in all aspects of quality and safety including but not limited to audits, HACCP program evaluation,…
$78,520 - $117,790 a year
4d
Engineering Laboratory Manager
Tech Talent Link —Kennewick, WA
Lab Team Ownership: Oversees and leads the Engineering Laboratory team in supporting both new development and post-release sustaining of Cadwell’s medical…
$140,000 - $165,000 a year
Quick Apply

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Senior Quality Manager
EDISON WELDING INSTITUTE INC —Columbus, OH
Define and own all quality policies, procedures, work instructions, and standards across manufacturing and engineering operations.
Quick Apply
QC Supervisor
WESTERMAN INC —Hebron, OH
Assists teams (including maintenance and engineering) with continuous improvement initiatives (driving safety, quality and process efficiencies).
$85,000 - $95,000 a year
Quick Apply
11d

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Quality Engineering Manager

GT Medical Technologies, Inc. -
Richland, WA

Quick Apply

Job Details

Full-time
$115,000 - $135,000 a year

Qualifications

Statistics
Computer operation
Managing projects in an engineering role
Quality control statistical data analysis
Statistical analysis
Bachelor's degree in engineering
Production validation processes
Quality risk management
Regulatory/legal compliance standards in production
Design controls
Biomedical regulatory compliance
Managing projects
Productivity software
Documentation Handling
Test validation method
ISO 13485
Cross-functional communication
FDA regulations
Customer complaint resolution

Full Job Description

Description:

Position Summary

The Quality Engineering Manager is responsible for leading the Quality Engineering department and ensuring the effective implementation, maintenance, and continuous improvement of quality engineering processes throughout the product lifecycle. This role manages a team of Quality Engineers responsible for product and process risk management, validation activities, supplier quality, component qualification, statistical analysis, complaint investigations, post-market surveillance, design history file maintenance, and support of the Corrective and Preventive Action (CAPA) system. The Quality Engineering Manager partners closely with Manufacturing, Operations, Technical Operations, Regulatory Affairs, Supply Chain, and Quality Assurance to ensure products consistently meet customer, regulatory, and company quality requirements while driving continuous improvement throughout the organization.

Job Duties/Responsibilities

Leadership & Team Management - Lead, mentor, and develop the Quality Engineering team by setting goals, managing staffing, workload, hiring, training, performance and career development, and overseeing daily operations, while fostering a culture of quality, accountability, continuous improvement, and compliance and serving as a liaison between management and staff.
Risk Management - Oversee product and process risk management across the lifecycle, ensuring compliant risk assessments, cross-functional reviews, and effective mitigation and documentation of identified risks.
Validation - Govern validation activities (process, equipment, software, and test method validation), ensuring protocols and reports meet regulatory and internal quality requirements.
Supplier Quality & Component Qualification - Lead supplier quality engineering activities, including supplier qualification, audits, performance monitoring, component qualification, first article reviews, investigations, corrective actions, and collaboration with Supply Chain to manage supplier performance and risk.
Statistical Analysis - Promote and provide guidance on the application of statistical methods to support product quality, process capability, validation, trend analysis, sampling, and continuous improvement.
Complaint Handling & Post-Market Surveillance - Lead complaint handling and post-market surveillance activities, including engineering support for investigations, trend analysis, risk identification, product performance monitoring, continuous improvement, and support for Medical Device Reporting (MDR) investigations.
CAPA & Nonconformance Support - Lead engineering support for nonconformance/CAPA investigations, including root cause analysis, corrective action, quality data analysis, and implementation of systemic improvements.
Design Quality - Oversee Design History File (DHF) maintenance and support design changes, risk assessments, verification, validation, design reviews, and design transfer activities.
Continuous Improvement - Drive continuous improvement across product quality, manufacturing, supplier performance, and quality systems through cross-functional Lean/Six Sigma projects and KPI development and monitoring.
Regulatory Compliance - Ensure Quality Engineering processes comply with FDA QMSR, ISO 13485, MDSAP, ISO 14971, and other applicable regulations, and support internal, external, supplier audits, and regulatory inspections.
Supervisory Responsibilities - Oversee daily team operations, including hiring, training, performance management, task assignment, communication, feedback, and employee relations, while serving as a liaison between management and staff to ensure productivity and a positive work environment.
Other - Embodies the Company’s purpose and shared values to foster a positive and productive team culture, complies with Company policies and procedures, accesses employee and/or patient PHI and ePHI only as required for job-related duties, and performs other duties as assigned.

Requirements:

Bachelor's degree in Engineering, Biomedical Engineering, Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, Chemical Engineering, or related technical discipline required.
Master's degree preferred.
Minimum of 8 years of progressive quality engineering experience in a regulated manufacturing environment.
Minimum of 3 years of leadership or supervisory experience preferred.
Medical device industry experience strongly preferred. ASQ Certified Quality Engineer (CQE) preferred
ASQ Certified Manager of Quality/Organizational Excellence (CMQ/OE) preferred
Six Sigma Green Belt or Black Belt preferred
Certified Reliability Engineer (CRE) or equivalent quality certification preferred
Demonstrated experience with validation, risk management, supplier quality, and quality systems.
Strong understanding of and proficiency Quality Management Systems (eQMS) and regulatory requirements.
Working knowledge of FDA Quality Management System regulations, ISO 13485, MDSAP, and ISO 14971 risk management principles.
Experience with Design Controls and Design History File management.
Thorough understanding of process validation methodologies and statistical analysis.
Knowledge of complaint handling, post-market surveillance, and supplier quality management.
Strong analytical and problem-solving abilities and organizational and decision-making skills.
Excellent written and verbal communication skills.
Ability to lead cross-functional teams and manage multiple complex projects.
Proficiency with Microsoft office programs and the Internet.
Willingness to work a flexible schedule and to travel as needed for work.
Satisfactorily pass comprehensive background screening and drug screening (if applicable to position).

Physical Demands/Working Conditions

Typical work environment for a professional office with work also conducted in a manufacturing environment (supply room, laboratory, and/or clean room).
Typically a stationary role with frequent moving from place to place.
Constant use of a computer, keyboard, mouse, monitor and other office equipment.
Occasionally picks up, carries, and moves items up to 50 lbs.
Potential exposure to hazardous materials requiring appropriate PPE and precautions when working with hazardous materials and chemicals.
Some evening and weekend work depending on workload.
Some overnight travel may be required for work, events, and training.

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Refine Your Search

quality assurance manager jobs in richland wa

Quality Engineering Manager

Team Leader Quality

QA/QC Manager

Enterprise Quality Assurance Manager/Team Leader

Food Safety Quality Assurance & Production Lead

Project Manager - Air Quality

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