Summary The Quality Assurance Engineer will support the organization towards compliance of ... Manage non-conformances, CAPA (Corrective and Preventive Action) processes, and root cause analysis.
Summary The Quality Assurance Engineer will support the organization towards compliance of ... Manage non-conformances, CAPA (Corrective and Preventive Action) processes, and root cause analysis.
Quality / Process Technician 2-month Contract
Greenfield, IN · On-site
$20 - $25/hr
This individual will perform inspections using CAPA-guided criteria, document findings, execute rework based on direction from the Quality Engineer, and support return material authorization (RMA ...
Quick apply
Quality / Process Technician 2-month Contract
Greenfield, IN · On-site
$20 - $25/hr
This individual will perform inspections using CAPA-guided criteria, document findings, execute rework based on direction from the Quality Engineer, and support return material authorization (RMA ...
Design Quality Engineer
Indianapolis, IN · On-site +1
Role Overview: The Design Quality Engineer will play a crucial role in supporting quality ... Support CAPA investigations, root cause analysis, and implementation of corrective actions.
Design Quality Engineer
Indianapolis, IN · On-site +1
Role Overview: The Design Quality Engineer will play a crucial role in supporting quality ... Support CAPA investigations, root cause analysis, and implementation of corrective actions.
The Quality Engineer develops, establishes and maintains quality engineering methodologies, systems ... CAPA systems to meet or exceed internal and external requirements. • Partner with cross ...
The Quality Engineer develops, establishes and maintains quality engineering methodologies, systems ... CAPA systems to meet or exceed internal and external requirements. • Partner with cross ...
The Quality Engineer develops, establishes and maintains quality engineering methodologies, systems ... CAPA systems to meet or exceed internal and external requirements. ● Partner with cross ...
The Quality Engineer develops, establishes and maintains quality engineering methodologies, systems ... CAPA systems to meet or exceed internal and external requirements. ● Partner with cross ...
The Quality Engineer develops, establishes and maintains quality engineering methodologies, systems ... Working knowledge of process controls, CAPA, root cause analysis and continuous improvement ...
The Quality Engineer develops, establishes and maintains quality engineering methodologies, systems ... Working knowledge of process controls, CAPA, root cause analysis and continuous improvement ...
Reporting to the Senior Advisor and partnering with Manufacturing, Quality Assurance, and Engineering, this role authors clear, defensible investigation reports and CAPA plans, performs hands-on ...
Reporting to the Senior Advisor and partnering with Manufacturing, Quality Assurance, and Engineering, this role authors clear, defensible investigation reports and CAPA plans, performs hands-on ...
Reporting to the Senior Advisor and partnering with Manufacturing, Quality Assurance, and Engineering, this role authors clear, defensible investigation reports and CAPA plans, performs hands-on ...
Reporting to the Senior Advisor and partnering with Manufacturing, Quality Assurance, and Engineering, this role authors clear, defensible investigation reports and CAPA plans, performs hands-on ...
Reporting to the Senior Advisor and partnering with Manufacturing, Quality Assurance, and Engineering, this role authors clear, defensible investigation reports and CAPA plans, performs hands-on ...
Reporting to the Senior Advisor and partnering with Manufacturing, Quality Assurance, and Engineering, this role authors clear, defensible investigation reports and CAPA plans, performs hands-on ...
Quality Compliance Engineer
Plainfield, IN · On-site
$85K - $95K/yr
Process engineering change requests (ECRs) and ensure proper documentation, approvals, and ... preventive actions (CAPA) * Create and maintain product master data within the ERP system ...
Quick apply
Quality Compliance Engineer
Plainfield, IN · On-site
$85K - $95K/yr
Process engineering change requests (ECRs) and ensure proper documentation, approvals, and ... preventive actions (CAPA) * Create and maintain product master data within the ERP system ...
Oversee the Corrective Action and Preventive Action (CAPA) process or designate a member of Quality ... Engineering Interns * Quality Engineers * Others as defined Following receipt of a conditional ...
Oversee the Corrective Action and Preventive Action (CAPA) process or designate a member of Quality ... Engineering Interns * Quality Engineers * Others as defined Following receipt of a conditional ...
Manufacturing & Quality Engineering Manager
Angola, IN · On-site
$90 - $120/hr
Oversee the Corrective Action and Preventive Action (CAPA) process or designate a member of Quality ... Quality Engineers* Others as definedFollowing receipt of a conditional offer of employment ...
Manufacturing & Quality Engineering Manager
Angola, IN · On-site
$90 - $120/hr
Oversee the Corrective Action and Preventive Action (CAPA) process or designate a member of Quality ... Quality Engineers* Others as definedFollowing receipt of a conditional offer of employment ...
Oversee the Corrective Action and Preventive Action (CAPA) process or designate a member of Quality ... Engineering Interns * Quality Engineers * Others as defined Following receipt of a conditional ...
Oversee the Corrective Action and Preventive Action (CAPA) process or designate a member of Quality ... Engineering Interns * Quality Engineers * Others as defined Following receipt of a conditional ...
Manufacturing & Quality Engineering Manager
Angola, IN · On-site
$90 - $140/hr
Oversee the Corrective Action and Preventive Action (CAPA) process or designate a member of Quality ... Quality Engineers* Others as definedFollowing receipt of a conditional offer of employment ...
Manufacturing & Quality Engineering Manager
Angola, IN · On-site
$90 - $140/hr
Oversee the Corrective Action and Preventive Action (CAPA) process or designate a member of Quality ... Quality Engineers* Others as definedFollowing receipt of a conditional offer of employment ...
Principal Scientist Deviation Management Lilly Medicine Foundry
Lebanon, IN · On-site
$65.25 - $169.40/hr
Partner with Manufacturing, Quality Assurance, Analytical/QC, Engineering, and AGL branch leads to scope investigations, verify corrective actions, and confirm CAPA effectiveness -- engaging the ...
Principal Scientist Deviation Management Lilly Medicine Foundry
Lebanon, IN · On-site
$65.25 - $169.40/hr
Partner with Manufacturing, Quality Assurance, Analytical/QC, Engineering, and AGL branch leads to scope investigations, verify corrective actions, and confirm CAPA effectiveness -- engaging the ...
Track corrective actions (CAPA). Maintain quality records. 2. Supervision & Team Leadership Supervise Quality Engineers and Quality Planning/Supplier Development Specialist. Provide daily direction ...
Track corrective actions (CAPA). Maintain quality records. 2. Supervision & Team Leadership Supervise Quality Engineers and Quality Planning/Supplier Development Specialist. Provide daily direction ...
Manufacturing Engineer
Warsaw, IN · On-site
$70K - $90K/yr
Medical Device Manufacturing Engineer Location: Warsaw, IN Duration: 6+ months Experience Required ... CAPA), and Work Instructions & Proficient with Statistical Process Control concepts Microsoft ...
Quick apply
Manufacturing Engineer
Warsaw, IN · On-site
$70K - $90K/yr
Medical Device Manufacturing Engineer Location: Warsaw, IN Duration: 6+ months Experience Required ... CAPA), and Work Instructions & Proficient with Statistical Process Control concepts Microsoft ...
The Supplier Quality Engineer is responsible for driving supplier quality performance, leading ... Action (CAPA) plans, support internal deviations related to logistics, and collaborate cross ...
The Supplier Quality Engineer is responsible for driving supplier quality performance, leading ... Action (CAPA) plans, support internal deviations related to logistics, and collaborate cross ...
The Supplier Quality Engineer is responsible for driving supplier quality performance, leading ... Action (CAPA) plans, support internal deviations related to logistics, and collaborate ...
The Supplier Quality Engineer is responsible for driving supplier quality performance, leading ... Action (CAPA) plans, support internal deviations related to logistics, and collaborate ...
Track corrective actions (CAPA). Maintain quality records. 2. Supervision & Team Leadership Supervise Quality Engineers and Quality Planning/Supplier Development Specialist. Provide daily direction ...
Quick apply
Track corrective actions (CAPA). Maintain quality records. 2. Supervision & Team Leadership Supervise Quality Engineers and Quality Planning/Supplier Development Specialist. Provide daily direction ...
Capa Engineer information
See Indiana salary details
$37.1K - $45.6K
3% of jobs
$45.6K - $54.2K
3% of jobs
$54.2K - $62.7K
4% of jobs
$62.7K - $71.2K
7% of jobs
$71.2K - $79.7K
6% of jobs
$80.4K is the 25th percentile. Wages below this are outliers.
$79.7K - $88.2K
6% of jobs
The median wage is $95.9K / yr.
$88.2K - $96.8K
21% of jobs
$96.8K - $105.3K
4% of jobs
$110.8K is the 75th percentile. Wages above this are outliers.
$105.3K - $113.8K
29% of jobs
$113.8K - $122.3K
2% of jobs
$122.3K - $130.8K
13% of jobs
$37.1K
$96.8K
$130.8K
How much do capa engineer jobs pay per year?
What is a CAPA engineer?
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.
What are the main daily responsibilities of a CAPA engineer?
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.
What are the key skills and qualifications needed to thrive in the CAPA engineer position, and why are they important?
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.
What are popular job titles related to Capa Engineer jobs in Indiana?
For Capa Engineer jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Capa Engineer jobs in Indiana look for?
The top searched job categories for Capa Engineer jobs in Indiana are:

Job description
Summary
The Quality Assurance Engineer will support the organization towards compliance of Corporate Quality and Environmental policies, provide leadership, expertise, and guidance for all Quality and Regulatory activities, and assist with required quality and technical tasks.
Essential Duties and Responsibilities
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
- Ensure compliance with FDA, ISO 13485, and other relevant regulatory standards for medical device manufacturing.
- Develop and implement quality management system documents for product design, development, and manufacturing.
- Conduct internal and external audits of quality systems to ensure adherence to quality standards.
- Coordinate the activities for Quality Management System (QMS) review and present the supporting data and metrics
- Review and approve manufacturing process changes impacting product quality, including changes to equipment and software
- Participate in risk management activities (FMEA, risk analysis) to identify potential product risks and implement corrective actions.
- Manage non-conformances, CAPA (Corrective and Preventive Action) processes, and root cause analysis.
- Collaborate on the investigations of customer complaints, ensure timely and accurate closure and issue reports back to affected customers.
- Work with cross-functional teams to resolve quality issues, including R&D, manufacturing, and regulatory departments.
- Develop and maintain quality documentation, including process validation protocols, technical reports, and device history records.
- Monitor and analyze quality data to identify trends and drive continuous improvement initiatives.
- Co-lead with R&D and Manufacturing Engineering the product, process and software validation activities (IQ, OQ, PQ) to ensure the product meets the required specifications.
- Co-lead with Sourcing the supplier qualification process and conduct regular audits to ensure that supplied components and raw materials meet quality requirements.
- Manage SCAR (Supplier Corrective Action Request) processto address and resolve quality issues arising from suppliers.
- Provide the tools and training on quality systems and procedures for internal teams.
- Ensure proper calibration and maintenance of quality inspection equipment.
- Other duties as assigned
Education and/or Experience
- Bachelor's degree in engineering (Mechanical, Electrical, Computer, Biomedical, Industrial, or related field) or equivalent experience.
- 5+ years of experience in quality assurance/quality engineering in a medical device or related industry.
- Strong understanding of regulatory requirements, including FDA 21 CFR 820, ISO 13485
- Experience with quality management systems, audits, and compliance.
- Experience with MasterControl eQMS is a plus.
- Proficiency in root cause analysis and corrective action (CAPA) processes.
- Strong analytical and problem-solving skills.
- Excellent verbal and written communication skills.
- Certified Quality Engineer (CQE) or equivalent certification is a plus.
- Familiarity with Six Sigma, Lean manufacturing, or other process improvement methodologies is a plus.
- Ability to manage multiple projects and work in a fast-paced environment.
- Knowledge of statistical process control (SPC) and other quality control tools is a plus.
- Proficiency in quality-related software tools (e.g., Minitab, QMS systems) is a plus.
Other Skills
- Language skills: Ability to read, analyze, and interpret the most complex documents. Ability to respond effectively to the most sensitive inquiries or complaints. Ability to make effective and persuasive speeches and presentations on controversial or complex topics to top management, public group, and/or boards of directors.
- Mathematical skills: Ability to work with mathematical concepts.
- Reasoning: Ability to define problems, collect data, establish facts and draw valid conclusions. Ability to interpret an extensive variety of information.
- Computer skills: Knowledge of Microsoft Office Suite
Competencies
- Communication: Effectively communicate to internal and external business partners by sharing expertise to encourage accomplishment of shared business goals.
- Teamwork and Collaboration: Actively support and collaborate with peers and team members to contribute to overall company success.
- Knowledge: Display knowledge of department, applicable products, services and business objectives. Demonstrate a continuous learning mindset through continued professional and personal development.
- Accountability: Follow through with tasks and responsibilities in an appropriate and timely manner.
- Work Quality: Produces results, meets goals, and provides services that meet or exceed EHOB's standards.
- Adaptability: Readily and effectively adapts way of working, thinking and acting in response to changing workplace conditions, targets or goals.
- Strategic Thinking: Demonstrate ability to understand a situation or obstacle from all perspectives.
- EHOB Ambassador: Reflect EHOB's mission, vision and values.
Work Environment
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts; risk of electrical shock; risk of radiation and vibration. The noise level in the work environment is usually moderate.
EHOB does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, sexual orientation, marital status, disability, genetic information, age, membership in an employee organization, retaliation, parental status or military service.
About Ehob
Sourced by ZipRecruiter
Industry
Medical equipment and supplies manufacturing
Company size
51 - 200 Employees
Headquarters location
Indianapolis, IN, US
Year founded
1985