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Quality Oversight Engineer Jobs in Virginia (NOW HIRING)

HII

$99K - $122K/yr

SUPPLIER QUALITY MECHANICAL ENGINEER 3 Location: Newport News, Virginia, United States Date: Aug 13 ... This oversight will include interfacing with suppliers in order to: audit/assess the supplier ...

Raymond

Senior Civil Engineer

Richmond, VA · On-site +1

Mentor and support junior engineers and designers, providing technical guidance and quality oversight. * Perform and review hydrologic and hydraulic analyses for stormwater management systems.

Jobtailor

Quality Engineer

Richmond, VA · On-site

$95 - $130/hr

Bachelor's degree in Engineering, Business, Computer Science, or a related technical discipline * 5+ years of experience in quality engineering or quality assurance, including oversight of third ...

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Quality Oversight Engineer information

What is a quality oversight engineer?

Quality Oversight Engineers are professionals responsible for ensuring that products, processes, and systems meet established quality standards and regulatory requirements. They monitor manufacturing or production operations, conduct audits, and collaborate with various teams to identify and resolve quality issues. Their role often includes reviewing documentation, implementing corrective actions, and ensuring compliance with industry regulations to maintain high-quality outputs. Additionally, they may provide training and guidance to staff on quality best practices and assist in continuous improvement initiatives.

How does a quality oversight engineer typically collaborate with cross-functional teams to ensure compliance and product quality?

Quality Oversight Engineers work closely with production, engineering, and regulatory teams to monitor processes and ensure adherence to quality standards. They often participate in project meetings, conduct audits, and review documentation to identify potential risks or non-conformities. Effective communication and teamwork are essential, as these engineers provide feedback, recommend corrective actions, and help implement process improvements. This collaborative environment helps maintain high product quality and regulatory compliance throughout the manufacturing lifecycle.

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

To thrive as a Quality Oversight Engineer, you need a solid background in quality management, engineering principles, and regulatory compliance, often supported by a degree in engineering or a related field. Familiarity with quality management systems (QMS), ISO standards, root cause analysis tools, and certifications such as Six Sigma or ASQ CQE are common requirements. Strong attention to detail, problem-solving abilities, and effective communication are vital soft skills to excel in this role. These competencies ensure that products and processes consistently meet standards, mitigate risks, and support organizational excellence.

What is the difference between Quality Oversight Engineer vs Quality Assurance Engineer?

AspectQuality Oversight EngineerQuality Assurance Engineer
CertificationsISO, Six Sigma, ASQ certifications often preferredISO, Six Sigma, ASQ certifications often preferred
Work EnvironmentRegulated industries like pharmaceuticals, medical devices, manufacturingSoftware, manufacturing, service industries
Primary FocusOverseeing compliance, audits, and quality systemsDeveloping and executing testing plans, process improvements
Employer UsageManufacturers, biotech, pharma companiesTech companies, manufacturing, software firms

While both roles focus on quality, the Quality Oversight Engineer primarily ensures compliance and oversees quality systems, often in regulated industries. The Quality Assurance Engineer concentrates on testing, process improvements, and preventing defects during product development. Understanding these differences helps candidates target the right roles based on their skills and industry focus.

Are quality oversight engineers paid well?

Quality oversight engineers typically earn competitive salaries that reflect their expertise in quality assurance, compliance, and process improvement. Compensation varies based on experience, industry, and location, but they generally receive benefits and opportunities for advancement in manufacturing, aerospace, or healthcare sectors.

Is a Quality Oversight Engineer a good career?

A Quality Oversight Engineer is a valuable role focused on ensuring product and process quality through inspections, audits, and compliance with standards. It often requires knowledge of quality management systems, industry regulations, and relevant certifications, making it a stable career with opportunities for advancement in manufacturing, healthcare, or technology sectors.

What are popular job titles related to Quality Oversight Engineer jobs in Virginia?

For Quality Oversight Engineer jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Quality Oversight Engineer jobs in Virginia look for?

The top searched job categories for Quality Oversight Engineer jobs in Virginia are:

What cities in Virginia are hiring for Quality Oversight Engineer jobs?

Cities in Virginia with the most Quality Oversight Engineer job openings:

Quality Oversight Engineer jobs near you

Senior Supplier Quality Engineer

Aurora Lifesciences

Manassas, VA • On-site

$85 - $110/hr

Other

Posted 3 days ago

New

Job description

Role Summary

The Senior Supplier Quality Engineer will ensure that logistics, warehousing, storage, handling, and distribution activities comply with medical device regulations and quality standards, including ISO 13485, EU MDR 2017/745, FDA 21 CFR Part 820, and GDP.

The role will provide quality oversight across the supply chain, from finished goods release through to customer delivery, supporting qualification audits, distribution controls, traceability, CAPA, risk management, validation, and continuous improvement.

Key Responsibilities
  • The Supplier Quality Engineer will ensure logistics, warehousing, storage, handling, and distribution processes comply with ISO 13485, GDP, EU MDR, FDA 21 CFR Part 820, and internal QMS requirements.
  • Support and improve QMS processes relating to warehousing, logistics, distribution, and product quality.
  • Act as quality SME for logistics and distribution processes during internal and external audits.
  • Provide quality oversight for product storage, packaging, labelling, shipment, environmental controls, and sterile medical device handling.
  • Review and approve shipping, transport validation, and related distribution documentation.
  • Maintain product traceability, including batch, lot, and serialisation controls where applicable.
  • Monitor logistics providers, warehouses, distributors, and external quality performance.
  • Plan, lead, and conduct qualification, surveillance, and remote audits.
  • Evaluate external partners against regulatory, internal, contractual, and customer requirements.
  • Prepare audit plans, checklists, reports, findings, non conformances, observations, and follow-up actions.
  • Ensure quality agreements are established, maintained, and compliant.
  • Investigate non conformances, investigations, deviations, complaints, and logistics-related quality issues.
  • Lead or support CAPA activities, including containment, root cause analysis, corrective actions, preventive actions, and effectiveness checks.
  • Support risk management activities, including ISO 14971, PFMEA review, change impact assessment, and non-conformance risk review.
  • Provide quality engineering support for process validation, equipment qualification, and transport validation activities.
  • Review and approve quality records, procedures, technical reports, and supporting documentation.
  • Analyse quality KPIs and drive continuous improvement across logistics and distribution processes.
Required Education and Experience
  • The Supplier Quality Engineer will hold a bachelor’s degree in Engineering, Science, or a relevant technical discipline.
  • Minimum 5 years’ quality experience in medical devices, pharmaceuticals, life sciences, or another regulated industry.
  • Strong knowledge of ISO 13485, EU MDR 2017/745, FDA 21 CFR Part 820, GDP, and medical device distribution requirements.
  • Experience with qualification audits, monitoring, quality agreements, non conformances, investigations, root cause analysis, CAPA, and risk management.
  • Familiarity with validation principles, including process validation, equipment qualification, and transport validation.
  • Working knowledge of Lean principles, Six Sigma tools, ERP systems, and QMS platforms.
  • ISO 13485 Lead Auditor certification required.
  • FDA QSR / 21 CFR Part 820 audit training required.
  • EU MDR training or qualification preferred.
Skills and Competencies
  • The Supplier Quality Engineer will have strong analytical, problem-solving, and root cause analysis skills.
  • High attention to detail and a strong compliance mindset.
  • Excellent documentation and technical writing skills.
  • Ability to apply risk-based thinking and process improvement methods.
  • Strong communication, stakeholder management, and cross-functional collaboration skills.
  • Ability to prioritise work, manage multiple tasks, and work independently in a regulated environment.
  • Hands-on approach with the ability to support logistics partners and internal teams.
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