Jobs in the United States

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Logistics Engineer
Brooklyn Park, MN
Caterpillar is seeking a Logistics Engineer in Brooklyn Park, MN. In this role, you will manage inbound and outbound material flow to ensure the timely and efficient movement of material to…
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Logistics Engineer
Victoria, TX
As the Logistics Engineer, you will lead the design, implementation, and continuous improvement of logistics processes that drive safety, efficiency, quality, and operational performance…
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Manufacturing Engineer
Pontiac, IL
The Manufacturing Engineer provides the technical expertise necessary to design, develop, and implement manufacturing systems, complex manufacturing operations and sophisticated machines.…
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Design Engineer
Alpharetta, GA
Caterpillar Switchgear, part of the Electric Power Division, currently has an opening for an Electrical Design Engineer located in Alpharetta, Georgia. In this role, you will design,…
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Manufacturing Engineer - CNC Programmer
East Peoria, IL
As a Manufacturing Engineer - CNC Programmer in East Peoria, Illinois, you will provide technical expertise that improves the safety, quality, cost, reliability, and efficiency of complex…
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Lead Software Engineer / .NET Full Stack (on-site)
Truist Bank
United States
Added 1 min ago
Staff Software Engineer
RealWork
Austin, TX
We're looking for a Staff Software Engineer to join our small but growing engineering team. The ideal candidate will have demonstrable expertise in product development, data engineering,…
Added 1 min ago
8
Senior Product Manager | Mobile
8am
Remote, United States
- $160,000 to $200,000 USD / year
Lead a two-engineer squad that works in small scopes, fast cycles, and frequent releases.
Added 1 min ago
Mechanical Design Engineer – Lead Steam Turbine Structure LP Hood Engineer (m/f/d)
GE Vernova Operations LLC
United States
The Lead Engineer – LP Hood will work closely with internal partners, interfacing with other teams such as steampath, rotor, thermodynamics, manufacturing, and the people on site, playing a…
Added 1 min ago
Senior Engineer - Robotics and Autonomous Systems - Vernova Research
GE Vernova Operations LLC
United States
The Senior Engineer – Robotics & Autonomous Systems is a senior technical contributor within the Robotics & Computer Vision team at GE Vernova Advanced Research. This role develops advanced…
Added 1 min ago
Lead CNC Programmer - Broach/Repair
GE Gas Turbines (Greenville) L.L.C.
United States
Provide CNC related support to M.E. (Manufacturing Engineer) and provide operator training during new / rebuilt machine startup and / or process improvements
Added 1 min ago
Manufacturing Engineer
GE Vernova Industrial of PR LLC
United States
Engineering associated with the manufacturing process. Accountable for the quality of own work. Subject to direct operations supervision/prescribed work instructions/systems checking.…
Added 1 min ago
Senior Software Engineer
STR
Dayton, OH · Arlington, VA · Atlanta, GA · Woburn, MA
As a Senior Software Engineer in SDD, you will design, develop, and test C++ software implementing complex embedded radar systems, with a primary focus on Air-to-Air applications.
Added 1 min ago
Senior Software Engineer
STR
Woburn, MA · Arlington, VA · Atlanta, GA · Dayton, OH
As a Senior Software Engineer in SDD, you will design, develop, and test C++ software implementing complex embedded radar systems, with a primary focus on Air-to-Air applications.
Added 1 min ago
Senior Software Engineer
STR
Arlington, VA · Atlanta, GA · Dayton, OH · Woburn, MA
As a Senior Software Engineer in SDD, you will design, develop, and test C++ software implementing complex embedded radar systems, with a primary focus on Air-to-Air applications.
Added 1 min ago
Senior Software Engineer
STR
Atlanta, GA · Arlington, VA · Dayton, OH · Woburn, MA
As a Senior Software Engineer in SDD, you will design, develop, and test C++ software implementing complex embedded radar systems, with a primary focus on Air-to-Air applications.
Added 2 mins ago
Sr. Product Engineer
Teledyne LeCroy, Inc.
Milpitas, CA
Coordinate new product introductions into the manufacturing process.
Added 2 mins ago
Component Engineer
Teledyne Controls, LLC
El Segundo, CA
Contribute to process improvements, including automation, data analytics, and AI‑enabled tools
Added 2 mins ago
Senior Software Development Engineer
Expedia, Inc.
WA
Added 2 mins ago
Mechanical Proposal Engineer
Plymouth, MI
Mechanical Proposal Engineer - Plymouth, Michigan
Added 2 mins ago
Yard and Dock Coordinator - 1st Shift
GXO Logistics
Lithia Springs, GA
Ensure dock activities align with process guidelines, safety standards, and site SWIs, seeing tasks through to completion
Added 2 mins ago
Clerk - 1st Shift
GXO Logistics
Moncks Corner, SC
Process orders and maintain inventory in a Warehouse Management System (WMS)
Added 2 mins ago
Warehouse Operations Supervisor - 1st Shift
GXO Logistics
Etna, OH
We engineer faster, smarter, leaner supply ch
Added 2 mins ago
Senior Software Development Engineer in Test
Arkestro
United States
Identifies and escalates any risk to quality of the product or the process
Added 3 mins ago
Forward-Deployed Engineer
Docusign
UNAVAILABLE · UNAVAILABLE, IL
…over 180 countries use Docusign solutions to accelerate the process of doing business and simplify people’s lives. With intelligent agreement management, Docusign unleashes…

Actalent

Quality Engineer Nonconformance & CAPA

Irvine, CA, United States

$40 to $55 USD / hour

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Job details

Pay: $40 to $55 USD / hour
Posting language: English
Posted: Nov 2, 2026

Original job description

Job Title: Quality EngineerJob DescriptionThe Quality Engineer supports quality activities within an on-site manufacturing operation, with primary responsibility for investigating and documenting manufacturing nonconformances across two production business units. The role focuses on identifying root causes of manufacturing and product issues, assessing impacted products and lots, and driving timely, compliant resolutions in a regulated environment.Responsibilities

Own and perform nonconformance investigations related to manufacturing and product quality issues across two production business units.
Conduct thorough root cause analysis to determine the source of manufacturing discrepancies and quality events.
Write clear, technically sound investigation reports that document findings, root cause, impacted lots and products, and recommended actions.
Support approximately four nonconformance closures per week, adapting to varying investigation complexity, timelines, and related change controls.
Partner with upstream and downstream teams to investigate issues across the entire manufacturing process, from raw materials to finished products.
Analyze manufacturing and quality data using tools such as Excel, Power BI, and PI Vision to identify trends, risks, and improvement opportunities.
Work cross-functionally with Operations, Quality, Manufacturing Engineering, supervisors, technicians, and production personnel to resolve quality issues.
Maintain complete, accurate, and compliant investigation documentation in accordance with applicable quality system requirements and good documentation practices (GDP).
Support and participate in CAPA activities, including risk mitigation and implementation of corrective and preventive actions stemming from investigations.
Contribute to and support change control processes associated with manufacturing and quality improvements.
Review drawings, procedures, and related technical documentation to ensure quality requirements are clearly defined and met.
Apply knowledge of regulatory expectations, including FDA and ISO-related requirements, within a medical device or pharmaceutical manufacturing context.
Support audits and internal quality assurance activities as needed.
Collaborate with cross-functional teams to continuously improve nonconformance investigation processes and overall product quality.

Essential Skills

Bachelor's degree in an engineering discipline or a related technical field.
Minimum 12+ years of professional industry experience after graduation.
13 years of experience within medical device or pharmaceutical manufacturing, or another regulated manufacturing environment.
Hands-on experience conducting nonconformance, NCR, NCMR, or deviation investigations, including ownership of investigations rather than only participation.
Demonstrated experience performing structured root cause analysis.
Experience with CAPA, risk mitigation, and change control in a manufacturing or production environment.
Proven ability to write high-quality technical investigation reports and other quality documentation.
Strong technical writing skills with attention to clarity, accuracy, and compliance with GDP.
Strong problem-solving skills with the ability to analyze complex manufacturing and quality issues.
Effective cross-functional communication skills, including the ability to work closely with Operations, Quality, Manufacturing Engineering, and production teams.
Experience supporting a manufacturing or production environment, including interaction with technicians, supervisors, and engineering staff.
Proficiency with Excel for data analysis and reporting.
Familiarity with FDA-regulated or ISO-based quality systems and quality engineering or quality assurance practices.

Additional Skills & Qualifications

Experience within medical device or pharmaceutical manufacturing environments is strongly preferred.
Exposure to or experience with Power BI and PI Vision for data visualization and analysis.
Experience in quality engineering, quality assurance, or related engineering disciplines.
Experience with audits in regulated manufacturing environments.
Knowledge of ISO standards relevant to quality systems and medical products.
Experience managing and documenting nonconformances, including NCMR and NCR processes.
Experience supporting investigations that lead to CAPA and change control activities.
Ability to interpret and review engineering drawings, procedures, and related technical documentation.
Comfort working in a growth-oriented organization with evolving processes and continuous improvement initiatives.
Interest in long-term assignment opportunities, with potential for a 12month contract and possible extension based on performance and business needs.

Work EnvironmentThis position is based on-site in a manufacturing environment that develops, manufactures, and markets innovative medical products and services for the healthcare industry. The facility focuses on products with inherent safety features that help address critical healthcare challenges, including opioid abuse issues, hospital-acquired malnutrition, and hazardous drug exposure. You will work closely with a large, diverse operations and quality team that includes technicians, supervisors, and engineering staff who manage raw materials, in-process work, and finished products. The environment is highly regulated and quality-focused, with established quality systems, FDA and ISO expectations, and strong emphasis on data-driven decision-making using tools such as Excel, Power BI, and PI Vision. The role involves regular interaction on the production floor, review of drawings and procedures, and participation in cross-functional projects. This is a 12month contract assignment with the potential to extend, offering the opportunity to contribute to a market-leading organization in a growth phase while supporting meaningful healthcare-focused products Job Type & LocationThis is a Contract to Hire position based out of Irvine, CA. Pay and BenefitsThe pay range for this position is $40.00 - $55.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits

available for this temporary role may include the following:

Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Job Type & LocationThis is a Contract to Hire position based out of Irvine, CA. Application DeadlineThis position is anticipated to close on Nov 13, 2026. Workplace TypeThis is a fully onsite position in Irvine,CA.About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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