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Continuous Improvement Engineer Jobs in Raleigh, NC

Qualcomm

CI Infrastructure Engineer

Raleigh, NC · On-site

$76K - $102K/yr

Qualcomm Technologies, Inc. is seeking an experienced CI Infrastructure Engineer to own and evolve the continuous integration infrastructure that supports their Machine Learning compiler stack. The ...

Qualcomm

CI Infrastructure Engineer

Raleigh, NC · On-site

$76K - $102K/yr

We are looking for an experienced CI Infrastructure Engineer to own and evolve the continuous integration (CI) infrastructure that supports our Machine Learning compiler stack. In this role, you will ...

Lancesoft

Process Validation Engineer3

Durham, NC · On-site

$52 - $54.85/hr

The role also drives training and capability development in Continuous Improvement methodologies and practices while leveraging technical expertise in Industrial Engineering and financial business ...

Exarca Inc.

Manufacturing Engineer

Raleigh, NC · On-site

$71K - $91K/yr

Manufacturing Engineer - Raleigh, NC (Onsite) We are seeking a Manufacturing Engineer to support product development, manufacturing, and continuous improvement initiatives. The ideal candidate will ...

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Showing results 21-40

All JobsContinuous Improvement Engineer JobsContinuous Improvement Engineer Jobs in Raleigh, NC

Continuous Improvement Engineer information

See Raleigh, NC salary details

$51K

$91.1K

$128.8K

How much do continuous improvement engineer jobs pay per year?

As of Aug 10, 2026, the average yearly pay for continuous improvement engineer in Raleigh, NC is $91,094.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,800.00 and $102,500.00 per year, depending on experience, location, and employer.

What is a continuous improvement engineer?

Continuous Improvement Engineers are professionals who analyze business processes and systems to identify areas for enhancement and increased efficiency. They use methodologies such as Lean, Six Sigma, and Kaizen to implement changes that reduce waste, improve quality, and streamline operations. Their role often involves working with cross-functional teams, collecting and analyzing data, and leading projects that drive sustainable improvements. These engineers play a critical part in helping organizations remain competitive and responsive to market demands.

What is the difference between Continuous Improvement Engineer vs Process Engineer?

AspectContinuous Improvement EngineerProcess Engineer
Primary FocusOptimizing processes through continuous improvement methodologiesDesigning, implementing, and improving manufacturing or operational processes
CertificationsLean, Six Sigma, KaizenSix Sigma, Lean, PMP (sometimes)
Work EnvironmentManufacturing plants, industrial settings, corporate officesManufacturing, production facilities, engineering departments
Industry UsageManufacturing, automotive, aerospace, healthcareManufacturing, chemical, electronics, energy

While both roles aim to improve efficiency, the Continuous Improvement Engineer primarily focuses on ongoing process enhancements using methodologies like Lean and Six Sigma. In contrast, the Process Engineer designs and refines specific processes to meet production goals. Both roles often collaborate but serve different aspects of operational improvement.

What are the key skills and qualifications needed to thrive as a continuous improvement engineer, and why are they important?

To thrive as a Continuous Improvement Engineer, you need a strong background in process optimization, data analysis, and problem-solving, often supported by a degree in engineering or a related field. Familiarity with Lean, Six Sigma methodologies, and tools such as Kaizen, Value Stream Mapping, and statistical analysis software is typically required, with certifications like Lean Six Sigma being highly valued. Strong communication, collaboration, and change management skills help drive initiatives and engage cross-functional teams. These competencies are essential for successfully identifying inefficiencies, implementing solutions, and fostering a culture of ongoing improvement within organizations.

How does a continuous improvement engineer typically collaborate with cross-functional teams to drive process enhancements?

Continuous Improvement Engineers frequently work alongside various departments, such as operations, quality, and supply chain, to identify inefficiencies and implement process improvements. They lead or participate in cross-functional teams, facilitating workshops like Kaizen events or root cause analyses to gather diverse perspectives. Effective communication and project management skills are essential, as these engineers must align stakeholders on goals, coordinate action plans, and track progress. This collaborative approach ensures that improvements are sustainable and have buy-in from all relevant areas of the organization.
More about Continuous Improvement Engineer jobs
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What job categories do people searching Continuous Improvement Engineer jobs in Raleigh, NC look for? The top searched job categories for Continuous Improvement Engineer jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Continuous Improvement Engineer jobs? Cities near Raleigh, NC with the most Continuous Improvement Engineer job openings:
Continuous Improvement Engineer jobs near you
Infographic showing various Continuous Improvement Engineer job openings in Raleigh, NC as of July 2026, with employment types broken down into 87% Full Time, 9% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $91,094 per year, or $43.8 per hour.

Senior Quality Engineer - Continuous Improvement

GILERO

Durham, NC • On-site

$83K - $113K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 10 days ago

Job description

Are you passionate about working to create high-quality, innovative medical and drug delivery devices to improve lives? As a Quality Engineer at Gilero, you’ll play a crucial role in ensuring the quality of life impacting medical devices and combination products. In this role you will provide oversight of the supplier management program and ensure continuous improvement of quality systems while supporting the design, development, and production of medical device and combination products.

This position can be based in our Durham Office or our Pittsboro Manufacturing Plant with options for hybrid work. Come join us and work in a collaborative and innovative environment where your contributions of ensuring products meet high standards will make a real difference.

Responsibilities:

  • Drive continuous improvement in quality and production processes by proactively identifying opportunities for improvement and developing action plans
  • Manage, trend, and continuously improve assigned quality system elements (CAPA, Complaints, Supplier Management, External Audits, etc.).
  • Execute quality event initiation, investigation, and closure for nonconformances, CAPA, change control and complaints. Perform effectiveness checks.
  • Facilitate investigations to determine root cause and failure modes.
  • Author new or revised procedures, train team members and release quality system procedures, as required.
  • Support internal and external audits including customer and supplier audits
  • Represent the quality function in product development projects providing support for development and commercialization activities. Author design history file documents during the development process.
  • Ensure compliant project documentation providing clear status and traceability in alignment with good documentation practices and controls hierarchy.
  • Investigate, disposition, and resolve nonconforming material events during product development, pre-production, and production phases.
  • Maintain quality records, summarize data, and report quality metrics to the organization.

Skills/Qualifications:

Required:

  • Bachelor's degree in engineering, science, or relevant field.
  • Minimum of 5 years quality experience in a regulated manufacturing and/or development environment.
  • Proficiency with FDA 820 CFRs/ISO 13485/cGMP quality management system and requirements for medical devices and combination product development and manufacturing.
  • Experience using risk analysis and continuous improvement concepts.
  • Extensive experience with GxP requirements.
  • Strong technical written and verbal communication skills.
  • Experience leading and/or supporting audits.
  • Excellent interpersonal, change management, planning and organizational skills.
  • Excellent oral, written, and presentation communication skills.

Preferred:

  • Master's or advanced degree in relevant field.
  • 5+ years in pharma or medical device manufacturing and/or development environment.
  • GxP terminology, experience and working knowledge in phase appropriate environments ranging from pre-clinical to commercial.
  • Project management experience.
  • CQE ASQ or related certification.

Personal Attributes:

  • Meets Gilero Core Values: Collaboration and Innovation of Excellence and Integrity
  • Productive in a fast-paced, entrepreneurial environment.
  • Commits to excellence and quality service to external and internal customers.
  • Adheres to established policies and procedures, while contributing to continuous improvements.


Eligibility To Work:

  • Applicants must be permanently authorized to work in the United States without the need for employer sponsorship now or in the future.
  • Gilero does not offer sponsorship for employment authorizations (work visas).
  • We are an E-Verify employer and confirm work authorization for all new hires.


Why work at Gilero?

Founded in 2002, Gilero, a Sanner Group company, is an international contract engineering firm that specializes in the design, development, and manufacturing of novel medical devices and drug delivery products. At Gilero, we are proud of the culture we have built that directly reflects our values of excellence, integrity, innovation, and collaboration. Motivated by our purpose to benefit people and improve patient outcomes, our team continues to grow at a rapid pace. US locations include Carlsbad, CA; Chicago, IL; as well as NC locations in Raleigh, Durham, Greensboro, and Pittsboro.


You will enjoy an annual bonus plan, Medical (3 BCBS plans to choose from), dental and vision, company-provided life insurance, short-term and long-term disability, 401(k) with a match the first month you start with a zero-vesting period, and access to LinkedIn learning for personal and professional development.

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About Gilero

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

51 - 200 Employees

Headquarters location

Durham, NC, US

Year founded

2002

Social media

Twitter

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