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Assistant Capa Engineer Jobs (NOW HIRING)

Abbott

Sr. Quality Systems/CAPA Engineer

Pleasanton, CA · On-site

$90K - $180K/yr

Represent Quality Systems as required in support of cross-functional projects * Assist in company ... Minimum 5 or more years of Engineering experience and demonstrated use of Quality tools ...

Abbott

Sr. Quality Systems/CAPA Engineer

Pleasanton, CA · On-site

$90K - $180K/yr

Represent Quality Systems as required in support of cross-functional projects * Assist in company ... Minimum 5or more years of Engineering experience and demonstrated use of Quality tools ...

Noblesoft Technologies

Lead Engineer

San Diego, CA · On-site

$108K - $143K/yr

Lead Engineer Location : Sandiego, CA JD: * Audits - independent set of eyes to review various ... assist CAPA owners * Knowledge of Global Hold process at MMS * Power Bi and ability to create ...

Validation & Engineering Group, Inc

PR

This role is responsible for supporting investigations, CAPA activities, change management ... * Assist with onboarding coordination activities, forms, access requests, and related compliance ...

Validation & Engineering Group, Inc

PR

This role is responsible for supporting investigations, CAPA activities, change management ... * Assist with onboarding coordination activities, forms, access requests, and related compliance ...

Validation & Engineering Group, Inc

PR

This role is responsible for supporting investigations, CAPA activities, change management ... * Assist with onboarding coordination activities, forms, access requests, and related compliance ...

Validation & Engineering Group, Inc

PR

This role is responsible for supporting investigations, CAPA activities, change management ... * Assist with onboarding coordination activities, forms, access requests, and related compliance ...

Validation & Engineering Group, Inc

PR

This role is responsible for supporting investigations, CAPA activities, change management ... * Assist with onboarding coordination activities, forms, access requests, and related compliance ...

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Assistant Capa Engineer information

See salary details

$33K

$88.8K

$134.5K

How much do assistant capa engineer jobs pay per year?

As of Jul 31, 2026, the average yearly pay for assistant capa engineer in the United States is $88,754.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $104,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Assistant CAPA Engineer, and why are they important?

To thrive as an Assistant CAPA Engineer, you need a solid understanding of quality management systems, root cause analysis, and regulatory compliance, generally supported by a degree in engineering or a related field. Familiarity with tools like CAPA software, Six Sigma methodologies, and ISO 13485 standards is typically required. Strong attention to detail, problem-solving skills, and effective communication are vital soft skills for this role. These competencies ensure effective corrective and preventive actions, regulatory compliance, and continuous improvement within quality-driven industries.

What are Assistant Capa Engineers?

Assistant CAPA (Corrective and Preventive Action) Engineers are entry- to mid-level professionals who support the implementation and management of CAPA processes within organizations, particularly in regulated industries like pharmaceuticals, medical devices, or manufacturing. Their main responsibilities include investigating quality-related issues, collecting and analyzing data, and helping to develop solutions that prevent recurrence of problems. They work closely with quality assurance teams to ensure compliance with industry standards and regulatory requirements. Assistant CAPA Engineers also help document CAPA activities and monitor the effectiveness of implemented solutions.

How does an Assistant CAPA Engineer typically collaborate with other departments during the corrective and preventive action (CAPA) process?

An Assistant CAPA Engineer frequently works alongside quality assurance, manufacturing, and regulatory teams to investigate root causes of non-conformances and implement effective corrective and preventive actions. This collaboration often involves gathering input from cross-functional teams, reviewing documentation, and participating in meetings to ensure that CAPA solutions are thorough and compliant with industry standards. Effective communication and teamwork are essential, as the Assistant CAPA Engineer must coordinate updates, track progress, and help ensure timely closure of CAPA items.

What is the difference between Assistant Capa Engineer vs Quality Control Engineer?

AspectAssistant Capa EngineerQuality Control Engineer
Required CredentialsEngineering degree, training in CAPA processesEngineering or science degree, QC certifications often preferred
Work EnvironmentManufacturing, pharmaceutical, or medical device industriesManufacturing, pharmaceutical, or food industries
Employer & Industry UsageUsed in industries focusing on corrective actions and complianceFocuses on product quality, testing, and inspection

The Assistant Capa Engineer primarily supports the implementation of Corrective and Preventive Actions (CAPA) to address quality issues, while the Quality Control Engineer focuses on testing and inspecting products to ensure quality standards. Both roles are essential in manufacturing and regulated industries, but they differ in their core responsibilities and focus areas.

What cities are hiring for Assistant Capa Engineer jobs? Cities with the most Assistant Capa Engineer job openings:
What are the most commonly searched types of Capa Engineer jobs? The most popular types of Capa Engineer jobs are:
What states have the most Assistant Capa Engineer jobs? States with the most job openings for Assistant Capa Engineer jobs include:
Assistant Capa Engineer jobs near you

Sr. Quality Systems/CAPA Engineer

Abbott

Pleasanton, CA • On-site

$90K - $180K/yr

Full-time

Medical, Retirement

Re-posted 5 days ago

Abbott rating

7.9

Company rating: 7.9 out of 10

Based on 136 frontline employees who took The Breakroom Quiz

158th of 536 rated manufacturers

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.
JOB DESCRIPTION:
Job Description
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
The Senior Quality Systems Engineer assures products conform to quality standards and establishes compliance with the quality system. Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success. The position employs an individual skilled in advance quality assurance techniques with an in-depth understanding of the ISO 13485 Quality Standard and US 21 CFR 820 QSR. Areas of focus will include improving quality system infrastructure, performance metrics and ISO, FDA and GMP compliance.
What You'll Work On
  • Assure compliance with corporate and divisional requirements regarding metrics reporting for the Management Controls / Management Review and CAPA quality systems.
  • Assure the collection, compiling, reporting and dissemination of key quality and compliance metrics/data are completed within the requiring timing.
  • Complete trend analysis of data as appropriate to ensure proper actions can be determined or assessed.
  • Perform and assure timely follow-up activities in support of key quality and compliance metric/data goals and policy/procedural requirements
  • Develop and provide data and analysis in support of Management Controls / Management Review and CAPA Quality Systems
  • Identify and implement opportunities for continuous improvement
  • Identify opportunities to apply, continuously improve, and redefine quality systems and controls product-related processes in accordance with applicable internal, domestic and international quality regulations, US 21 CFR 820 (QSR), ISO 13485, etc.
  • Represent Quality Systems as required in support of cross-functional projects
  • Assist in company preparations for hosting external audits
  • Participate in external and internal audits
  • Assists management teams to ensure timely closure of audit observations. Lead non-conformance investigation teams to identify root causes and effective CAPAs
  • Lead, coach, and mentor non-exempt and entry level exempt personnel on quality principles and procedures
  • Function as part of risk assessment teams to identify product, quality system and compliance requirements.
  • Function as part of special project teams to identify compliance gaps and develop and execute strategies to close gaps.

Required Qualifications :
  • Bachelor's degree in engineering or Technical Field
  • Minimum 5 or more years of Engineering experience and demonstrated use of Quality tools/methodologies
  • knowledge of FDA820, GMP, ISO 13485, and ISO 14971

Preferred Qualifications:
  • Project management and leadership skills, including the demonstrated ability to lead multi-departmental project teams and resolve quality-related issues
  • Internal and External Audit experience
  • MS or higher degree in a technical discipline
  • Advanced computer skills, including statistical/data analysis and report writing skills
  • medical device industry experience
  • ASQ CQE or CQA certification

Apply Now
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 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
$90,000.00 - $180,000.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Operations Quality
DIVISION:
HF Heart Failure
LOCATION:
United States > Pleasanton : 6101 Stoneridge Dr
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 10 % of the Time
MEDICAL SURVEILLANCE:
No
SIGNIFICANT 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)
Abbott 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.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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