El Paso, TX · On-site
$65K - $84K/yr
The CAPA Engineer is responsible for leading and facilitating the Corrective and Preventive Action (CAPA) process to ensure effective resolution of quality issues, nonconformances, audit findings ...
El Paso, TX · On-site
$65K - $84K/yr
The CAPA Engineer is responsible for leading and facilitating the Corrective and Preventive Action (CAPA) process to ensure effective resolution of quality issues, nonconformances, audit findings ...
El Paso, TX · On-site
$65K - $84K/yr
The CAPA Engineer is responsible for leading and facilitating the Corrective and Preventive Action (CAPA) process to ensure effective resolution of quality issues, nonconformances, audit findings ...
El Paso, TX · On-site
$65K - $84K/yr
The CAPA Engineer is responsible for leading and facilitating the Corrective and Preventive Action (CAPA) process to ensure effective resolution of quality issues, nonconformances, audit findings ...
El Paso, TX · On-site
$65K - $84K/yr
The CAPA Engineer is responsible for leading and facilitating the Corrective and Preventive Action (CAPA) process to ensure effective resolution of quality issues, nonconformances, audit findings ...
El Paso, TX · On-site
$65K - $84K/yr
The CAPA Engineer is responsible for leading and facilitating the Corrective and Preventive Action (CAPA) process to ensure effective resolution of quality issues, nonconformances, audit findings ...
Trumbull, CT · On-site
$86K - $117K/yr
The Sr. Global CAPA Engineer serves as a subject matter expert for the Global Corrective and Preventive Action (CAPA) Program, providing technical leadership, facilitation, and guidance to ensure ...
Trumbull, CT · On-site
$86K - $117K/yr
The Sr. Global CAPA Engineer serves as a subject matter expert for the Global Corrective and Preventive Action (CAPA) Program, providing technical leadership, facilitation, and guidance to ensure ...
Trumbull, CT · On-site
$86K - $117K/yr
The Sr. Global CAPA Engineer serves as a subject matter expert for the Global Corrective and Preventive Action (CAPA) Program, providing technical leadership, facilitation, and guidance to ensure ...
Trumbull, CT · On-site
$86K - $117K/yr
The Sr. Global CAPA Engineer serves as a subject matter expert for the Global Corrective and Preventive Action (CAPA) Program, providing technical leadership, facilitation, and guidance to ensure ...
Trumbull, CT · On-site
$86K - $117K/yr
The Sr. Global CAPA Engineer serves as a subject matter expert for the Global Corrective and Preventive Action (CAPA) Program, providing technical leadership, facilitation, and guidance to ensure ...
Trumbull, CT · On-site
$86K - $117K/yr
The Sr. Global CAPA Engineer serves as a subject matter expert for the Global Corrective and Preventive Action (CAPA) Program, providing technical leadership, facilitation, and guidance to ensure ...
Rancho Santa Margarita, CA · On-site
$72K - $78K/yr
As a Quality Engineer I, you will learn and develop skills to support medical device quality ... Perform oversight and approval of Corrective and Preventative Actions (CAPA) * Conduct experiments ...
Rancho Santa Margarita, CA · On-site
$72K - $78K/yr
As a Quality Engineer I, you will learn and develop skills to support medical device quality ... Perform oversight and approval of Corrective and Preventative Actions (CAPA) * Conduct experiments ...
NY · On-site
$70K - $91K/yr
Participate in engineering design reviews and make recommendations to improve the quality and manufacturability of new designs * Provide quality assurance domain expertise across the enterprise
NY · On-site
$70K - $91K/yr
Participate in engineering design reviews and make recommendations to improve the quality and manufacturability of new designs * Provide quality assurance domain expertise across the enterprise
Cambridge, MA · On-site
$78K - $101K/yr
Responsible for performing timely, detailed CAPA engineering tasks like assessing issue descriptions, reviewing CAPA data sources, assisting with root cause analysis, and quality problem-solving.
Cambridge, MA · On-site
$78K - $101K/yr
Responsible for performing timely, detailed CAPA engineering tasks like assessing issue descriptions, reviewing CAPA data sources, assisting with root cause analysis, and quality problem-solving.
Newark, DE · On-site
$97K - $152K/yr
Hologic is seeking a Quality Engineer, CAPA Facilitator to support and strengthen Corrective and Preventive Action, CAPA, processes and broader quality assurance operations. This role will partner ...
Newark, DE · On-site
$97K - $152K/yr
Hologic is seeking a Quality Engineer, CAPA Facilitator to support and strengthen Corrective and Preventive Action, CAPA, processes and broader quality assurance operations. This role will partner ...
Newark, DE · On-site
$97K - $152K/yr
Hologic is seeking a Quality Engineer, CAPA Facilitator to support and strengthen Corrective and Preventive Action, CAPA, processes and broader quality assurance operations. This role will partner ...
Newark, DE · On-site
$97K - $152K/yr
Hologic is seeking a Quality Engineer, CAPA Facilitator to support and strengthen Corrective and Preventive Action, CAPA, processes and broader quality assurance operations. This role will partner ...
Itasca, IL · On-site
$100K - $115K/yr
Minimum of four years of relevant industry experience in medical devices, complaint investigation, CAPA, quality engineering, manufacturing, supplier quality, service and repair, reliability, or post ...
Quick apply
Itasca, IL · On-site
$100K - $115K/yr
Minimum of four years of relevant industry experience in medical devices, complaint investigation, CAPA, quality engineering, manufacturing, supplier quality, service and repair, reliability, or post ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
Maple Grove, MN · On-site
$102K - $194K/yr
Create Alert Principal Quality System Engineer - CAPA Onsite Location(s): Maple Grove, MN, US, 55311 Principal Quality System Engineer - CAPA About the role: As a Principal Quality System Engineer ...
Maple Grove, MN · On-site
$102K - $194K/yr
Create Alert Principal Quality System Engineer - CAPA Onsite Location(s): Maple Grove, MN, US, 55311 Principal Quality System Engineer - CAPA About the role: As a Principal Quality System Engineer ...
Salt Lake City, UT · On-site
Collaborate with Quality, Regulatory Affairs, Engineering, Manufacturing, Supplier Quality, Complaint Handling, Service, and other functions to ensure CAPA inputs and related quality records are ...
Salt Lake City, UT · On-site
Collaborate with Quality, Regulatory Affairs, Engineering, Manufacturing, Supplier Quality, Complaint Handling, Service, and other functions to ensure CAPA inputs and related quality records are ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
Salt Lake City, UT · On-site
Collaborate with Quality, Regulatory Affairs, Engineering, Manufacturing, Supplier Quality, Complaint Handling, Service, and other functions to ensure CAPA inputs and related quality records are ...
Salt Lake City, UT · On-site
Collaborate with Quality, Regulatory Affairs, Engineering, Manufacturing, Supplier Quality, Complaint Handling, Service, and other functions to ensure CAPA inputs and related quality records are ...
Salt Lake City, UT · On-site
Lead and develop quality analysts, quality engineers, or CAPA coordinators as applicable; provide coaching on quality systems, investigations, regulatory expectations, and talent development.
Salt Lake City, UT · On-site
Lead and develop quality analysts, quality engineers, or CAPA coordinators as applicable; provide coaching on quality systems, investigations, regulatory expectations, and talent development.
$39K - $48K
3% of jobs
$48K - $56.9K
3% of jobs
$56.9K - $65.9K
4% of jobs
$65.9K - $74.8K
7% of jobs
$74.8K - $83.8K
6% of jobs
$84.5K is the 25th percentile. Wages below this are outliers.
$83.8K - $92.7K
6% of jobs
The median wage is $100.8K / yr.
$92.7K - $101.7K
21% of jobs
$101.7K - $110.6K
4% of jobs
$116.4K is the 75th percentile. Wages above this are outliers.
$110.6K - $119.6K
29% of jobs
$119.6K - $128.5K
2% of jobs
$128.5K - $137.5K
13% of jobs
$39K
$101.8K
$137.5K
A CAPA (Corrective and Preventive Action) Engineer is responsible for identifying, investigating, and resolving quality issues in manufacturing or engineering processes. They analyze root causes of defects, implement corrective measures, and develop preventive strategies to ensure compliance with industry regulations. CAPA Engineers work closely with cross-functional teams to improve product quality, streamline processes, and maintain regulatory compliance. They also document findings, track action plans, and support continuous improvement initiatives to reduce future risks.
A CAPA Engineer's daily responsibilities typically include investigating potential or actual nonconformities, conducting root cause analyses, and developing corrective and preventive action plans to resolve and prevent future issues. They also collaborate closely with cross-functional teams such as manufacturing, quality assurance, and regulatory affairs to ensure solutions are practical and compliant with industry standards. Additionally, CAPA Engineers monitor the progress and effectiveness of implemented actions, prepare documentation for audits, and participate in continuous process improvement initiatives. This role is crucial for maintaining the highest quality standards and ensuring compliance in regulated industries such as medical devices or pharmaceuticals.
To thrive as a CAPA Engineer, you need a solid background in quality engineering, root cause analysis, and process improvement, typically supported by a degree in engineering or a related technical field. Familiarity with CAPA management systems, quality standards such as ISO 13485 or ISO 9001, and tools like Six Sigma or FMEA is highly valuable. Strong problem-solving abilities, attention to detail, and effective communication skills distinguish top performers in this role. These competencies ensure effective identification, documentation, and resolution of quality issues, helping organizations maintain regulatory compliance and deliver high-quality products.
Cities with the most Capa Engineer job openings:
The most popular types of Capa Engineer jobs are:
States with the most job openings for Capa Engineer jobs include:
For Capa Engineer jobs, the most frequently searched job titles are:
El Paso, TX • On-site
$65K - $84K/yr
Full-time
Medical, Dental, Retirement
Posted 13 days ago
7.3
Based on 143 frontline employees who took The Breakroom Quiz
We are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job DescriptionThis position is a Fixed Term (limited-term) assignment from 10/1/26 to 10/1/27 designed to support a specific business need. Associates in this role are eligible for BD benefits, including medical, dental, health, and 401(k), subject to the eligibility requirements of BD Total Rewards policies. Employment is intended for a defined period and is expected to conclude upon completion of the assignment or fulfillment of the associated business objective.
CAPA Management
Lead CAPA investigations from initiation through closure.
Ensure CAPAs are completed on time and comply with internal procedures and regulatory requirements.
Facilitate cross-functional investigation teams.
Maintain CAPA records and supporting documentation within electronic quality management systems (e.g., TrackWise).
Monitor CAPA status and escalate risks, delays, or resource constraints when necessary.
Root Cause Analysis
Conduct and facilitate root cause investigations using appropriate methodologies, which may include
5 Whys
Fishbone (Ishikawa)
DMAIC
SOLV
PDCA
Ensure investigations are evidence-based, systematic, and adequately documented.
Determine true root causes and contributing factors.
Corrective and Preventive Actions
Develop effective corrective and preventive action plans.
Collaborate with process owners to implement sustainable solutions.
Evaluate proposed actions for effectiveness and regulatory compliance.
Verify implementation and completion of assigned actions.
Ensure actions address both immediate and systemic causes.
Effectiveness Verification
Define objective effectiveness criteria.
Perform effectiveness checks to confirm actions have mitigated or eliminated root causes.
Analyze post-implementation data and trends.
Recommend additional actions when effectiveness criteria are not met.
Metrics and Continuous Improvement
Monitor CAPA performance metrics, aging, and effectiveness.
Identify recurring quality issues and systemic trends.
Support continuous improvement initiatives and quality system enhancements.
Develop management reports and quality review presentations.
Regulatory and Compliance Support
Support internal, external, customer, and regulatory audits.
Provide CAPA documentation and investigation support during inspections.
Ensure compliance with:
21 CFR Part 820 / QMSR
ISO 13485
Company Quality System Procedures
Support inspection readiness activities.
Qualifications
Education
Bachelor's degree in Engineering, Quality, Life Sciences, Manufacturing, or related technical discipline.
Experience
3 to 7 years of experience in Quality Engineering, Quality Systems, Manufacturing Quality, or CAPA management.
Medical device, pharmaceutical, biotechnology, or regulated industry experience preferred.
Experience leading investigations and root cause analysis activities.
Technical Skills
CAPA Management Systems (TrackWise preferred)
Root Cause Analysis methodologies
Risk Management principles
Data analysis and trending
Quality System Regulations
Statistical tools and quality improvement methods
Microsoft Office and reporting tools
Competencies
Strong analytical and critical thinking skills
Excellent investigation and problem-solving abilities
Ability to influence cross-functional teams without direct authority
Effective project management and prioritization skills
Strong written and verbal communication
Attention to detail and documentation quality
Ability to manage multiple priorities in a fast-paced environment
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
To learn more about BD visit https://bd.com/careers.
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
Required Skills
Optional Skills
.
Primary Work LocationUSA TX - El Paso - Northwestern Dr.Additional LocationsWork Shift
Sourced by ZipRecruiter
BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.
Medical equipment and supplies manufacturing and manufacturing
10,000+ Employees
Franklin Lakes, NJ, US
