As a CAPA Coordinator , you will manage the plant's GMP Investigations and Corrective and ... Bachelor's degree required (Business, Science, Engineering, Math/Statistics, or related field ...
As a CAPA Coordinator , you will manage the plant's GMP Investigations and Corrective and ... Bachelor's degree required (Business, Science, Engineering, Math/Statistics, or related field ...
Collaborate cross-functionally with Quality, Manufacturing, Engineering, Technical Operations, and Procurement to develop and implement effective CAPA solutions. * Facilitate meetings and drive ...
Collaborate cross-functionally with Quality, Manufacturing, Engineering, Technical Operations, and Procurement to develop and implement effective CAPA solutions. * Facilitate meetings and drive ...
As a CAPA Coordinator , you will manage the plant's GMP Investigations and Corrective and ... Bachelor's degree required (Business, Science, Engineering, Math/Statistics, or related field ...
As a CAPA Coordinator , you will manage the plant's GMP Investigations and Corrective and ... Bachelor's degree required (Business, Science, Engineering, Math/Statistics, or related field ...
CAPA/NCR Writer
Round Lake, IL · On-site
CAPA/NCR Writer Duration: 06 Months Location: Round Lake, IL Only W2 candidates are eligible for ... engineering or related field is required. • 2-5 years relevant work experience in cGMP related ...
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CAPA/NCR Writer
Round Lake, IL · On-site
CAPA/NCR Writer Duration: 06 Months Location: Round Lake, IL Only W2 candidates are eligible for ... engineering or related field is required. • 2-5 years relevant work experience in cGMP related ...
CAPA Execution Specialist/Investigator (Medical Device Manufacturing)
Wilmington, DE · On-site
$40 - $50/hr
CAPA Execution Specialist / Investigator Location: Delaware (Onsite) Employment Type: Contract (W2 ... Engineering, or related field · Hands-on experience executing CAPAs in medical device ...
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CAPA Execution Specialist/Investigator (Medical Device Manufacturing)
Wilmington, DE · On-site
$40 - $50/hr
CAPA Execution Specialist / Investigator Location: Delaware (Onsite) Employment Type: Contract (W2 ... Engineering, or related field · Hands-on experience executing CAPAs in medical device ...
PR · On-site
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role is responsible for supporting investigations, CAPA activities, change management ...
Quick apply
PR · On-site
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role is responsible for supporting investigations, CAPA activities, change management ...
PR · On-site
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role is responsible for supporting investigations, CAPA activities, change management ...
Quick apply
PR · On-site
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role is responsible for supporting investigations, CAPA activities, change management ...
PR · On-site
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role is responsible for supporting investigations, CAPA activities, change management ...
Quick apply
PR · On-site
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role is responsible for supporting investigations, CAPA activities, change management ...
PR · On-site
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role is responsible for supporting investigations, CAPA activities, change management ...
Quick apply
PR · On-site
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role is responsible for supporting investigations, CAPA activities, change management ...
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role is responsible for supporting investigations, CAPA activities, change management ...
Quick apply
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role is responsible for supporting investigations, CAPA activities, change management ...
Sales Quality Engineer
$78K - $101K/yr
Facilitate CAPA meetings with cross-functional stakeholders and monitor progress, effectiveness ... Sales Engineers * Customer Service * After Sales * Planning/Purchasing * Supply Chain and ...
Sales Quality Engineer
$78K - $101K/yr
Facilitate CAPA meetings with cross-functional stakeholders and monitor progress, effectiveness ... Sales Engineers * Customer Service * After Sales * Planning/Purchasing * Supply Chain and ...
Quality Senior Engineer I - Englewood, CO - Onsite
Englewood, CO · On-site
$87K - $118K/yr
Englewood, CO - Onsite Duration: 12 Months Duties · Review, remediate, and migrate legacy CAPA ... S. in engineering or an alternative Bachelor's degree program 3-5 years of experience required in a ...
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Quality Senior Engineer I - Englewood, CO - Onsite
Englewood, CO · On-site
$87K - $118K/yr
Englewood, CO - Onsite Duration: 12 Months Duties · Review, remediate, and migrate legacy CAPA ... S. in engineering or an alternative Bachelor's degree program 3-5 years of experience required in a ...
Sr. Quality Engineer (Wayne, NJ)
Wayne, NJ · Hybrid
$87K - $119K/yr
Lead or support CAPA investigations, including data collection, analysis, and documentation ... Provide guidance to junior engineers on investigations and documentation * Contribute to cross ...
Sr. Quality Engineer (Wayne, NJ)
Wayne, NJ · Hybrid
$87K - $119K/yr
Lead or support CAPA investigations, including data collection, analysis, and documentation ... Provide guidance to junior engineers on investigations and documentation * Contribute to cross ...
This opportunity is ideal for professionals with strong experience in Supplier Quality, CAPA, Risk ... Engineering or a related technical discipline.
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This opportunity is ideal for professionals with strong experience in Supplier Quality, CAPA, Risk ... Engineering or a related technical discipline.
Senior Quality Systems Engineer
Alpharetta, GA · On-site
$84K - $114K/yr
CAPA Management * Act as a subject matter expert (SME) for CAPA, non-conforming product, deviations (quality non-conformance) and compliance-related activities. * Lead the end-to-end CAPA, non ...
Senior Quality Systems Engineer
Alpharetta, GA · On-site
$84K - $114K/yr
CAPA Management * Act as a subject matter expert (SME) for CAPA, non-conforming product, deviations (quality non-conformance) and compliance-related activities. * Lead the end-to-end CAPA, non ...
Sr. Quality Engineer (Wayne, NJ)
Wayne, NJ · On-site
$87K - $119K/yr
Lead or support CAPA investigations, including data collection, analysis, and documentation ... Provide guidance to junior engineers on investigations and documentation * Contribute to cross ...
Sr. Quality Engineer (Wayne, NJ)
Wayne, NJ · On-site
$87K - $119K/yr
Lead or support CAPA investigations, including data collection, analysis, and documentation ... Provide guidance to junior engineers on investigations and documentation * Contribute to cross ...
The ideal candidate will have strong experience in supplier quality, CAPA investigations, risk ... Required Qualifications • 5+ years of Supplier Quality Engineering experience. • Medical Device ...
Quick apply
The ideal candidate will have strong experience in supplier quality, CAPA investigations, risk ... Required Qualifications • 5+ years of Supplier Quality Engineering experience. • Medical Device ...
Development Engineer
Raynham, MA · On-site
$75K - $120K/yr
Lead and participate in project core teams, liaising with QA, RA, Clinical, R&D, Manufacturing, and Production Engineering as part of CAPA, continuous improvement, and optimization projects.
Development Engineer
Raynham, MA · On-site
$75K - $120K/yr
Lead and participate in project core teams, liaising with QA, RA, Clinical, R&D, Manufacturing, and Production Engineering as part of CAPA, continuous improvement, and optimization projects.
Career Development and Internship Specialist
Phoenix, AZ · On-site
$52K/yr
Support Institutional Relations Regional Directors & Partnership Directors in the promotion of CEA CAPA's Career & Internship Programming and support services to prospective students and U.S ...
Career Development and Internship Specialist
Phoenix, AZ · On-site
$52K/yr
Support Institutional Relations Regional Directors & Partnership Directors in the promotion of CEA CAPA's Career & Internship Programming and support services to prospective students and U.S ...
Quality Engineer
Northfield, IL · On-site
$74K - $96K/yr
Hands-on experience with DHF, CAPA, Design Control, and Risk Management * Experience in regulated ... Bachelor's degree in Engineering, Science, Mathematics, or related technical field. Thanks ...
Quick apply
Quality Engineer
Northfield, IL · On-site
$74K - $96K/yr
Hands-on experience with DHF, CAPA, Design Control, and Risk Management * Experience in regulated ... Bachelor's degree in Engineering, Science, Mathematics, or related technical field. Thanks ...
CAPA Engineer information
See salary details
$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
How much do capa engineer jobs pay per year?
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 is a CAPA Engineer job?
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.

Full-time
Medical, Retirement
Posted 25 days ago
Abbott rating
7.9
Based on 136 frontline employees who took The Breakroom Quiz
154th of 527 rated manufacturers
Job description
Abbott Nutrition in Casa Grande, AZ is seeking a CAPA Coordinator.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:
Career development with an international company where you can grow the career you dream of.
Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
An excellent retirement savings plan with a high employer contribution
Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
This position works out of our Casa Grande, Arizona location in the Abbott Nutrition division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands - including Similac, PediaSure, Pedialyte, Ensure, and Glucerna - to help them get the nutrients they need to live their healthiest lives.
Casa Grande, AZ., is one of Abbott's leading nutrition manufacturing plants in the U.S., reflecting our commitment to innovation and excellence. But we're more than just a company, we're a family. Working here you'll be part of a family that works together to make a difference and enhance the lives of millions worldwide.
What You'll Work On
The primary responsibilities of the CAPA Coordinator are multifunctional and include management of the plant GMP/Investigations and Corrective Action/Preventative Action (CAPA) program. Primary responsibilities include implementation and maintenance in the following areas:
Leading and writing complex investigations, including thorough root cause analysis
Driving the development and implementation of corrective and preventive actions (CAPA)
Serving as a technical resource for investigation and root cause methodologies
Training employees on investigation and CAPA systems and processes
Ensuring all investigations and CAPA activities meet GMP, corporate, and regulatory standards
Major Responsibilities:
Implement, maintain, and continuously improve the CAPA Quality System
Monitor CAPA program effectiveness, including metrics, trend analysis, and on-time completion of actions
Prepare and present CAPA data for monthly and quarterly management reviews
Review non-conformances impacting product quality and recommend corrective actions and effectiveness checks
Ensure investigation and CAPA documentation complies with GMP, corporate policies, and industry standards
Partner with cross-functional teams to identify root causes and implement sustainable solutions
Ensure proper review and approval of all investigations
Train site personnel on CAPA processes and best practices
Lead the Site PoP (Protect Our Product) Program, including mentoring workstream leads and acting as a liaison with division teams
You'll be accountable for meeting our compliance standards including FDA, OSHA and Abbott policies and procedures.
Required Qualifications
Bachelor's degree required (Business, Science, Engineering, Math/Statistics, or related field)
Preferred Qualifications
Master's degree preferred
4+ years of quality assurance experience in a GMP-regulated industry
Knowledge of regulatory requirements for infant formula and medical nutrition products
Understanding of food processing, laboratory procedures, documentation practices, and statistical applications
Strong written and verbal communication skills
Proven ability to prioritize, manage multiple projects, and meet deadlines
Demonstrated critical thinking, problem-solving, and analytical skills
Ability to collaborate effectively across all levels of the organization
This is a Day shift opportunity
In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire. Pre-Employment Inquiries and Citizenship | U.S. Equal Employment Opportunity Commission (eeoc.gov)
Apply Now
* Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity and Military/Veteran friendly Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.
The base pay for this position is
$86,700.00 - $173,300.00In specific locations, the pay range may vary from the range posted.
JOB FAMILY:Operations QualityDIVISION:ANSC Nutrition Supply ChainLOCATION:United States > Casa Grande : PlantADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:NoMEDICAL SURVEILLANCE:NoSIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day), Wear ear plugs, Work in a clean room environmentAbbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf