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Supplier Quality Engineering Jobs (NOW HIRING)

Working with cross-functional commodity teams, the Supplier Quality Engineer represents the quality ... At least 3 to 5 years experience in a manufacturing or quality engineering environment. Ability to ...

Working with cross-functional commodity teams, the Supplier Quality Engineer represents the quality ... At least 3 to 5 years experience in a manufacturing or quality engineering environment. Ability to ...

Bachelor's degree - Science/Engineering/Electrical Engineering is desirable. * Knowledge of Global ... Benefits of the Supplier Quality Engineer * Competitive salary * Advancement potential ...

Partner with development engineering, product quality engineering, product sourcing engineering, Global Strategic Sourcing and program management to deliver predictable supply to the development ...

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Supplier Quality Engineering information

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$35

$69

How much do supplier quality engineering jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for supplier quality engineering in the United States is $35.45, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $60.82 per hour, depending on experience, location, and employer.

What is supplier quality engineering?

Supplier Quality Engineering (SQE) is a specialized field that focuses on ensuring that materials, components, and products sourced from suppliers meet an organization's quality standards and requirements. Supplier Quality Engineers work closely with suppliers to develop quality assurance processes, perform audits, and resolve quality issues. Their role is vital in maintaining product reliability, compliance, and minimizing defects or recalls. SQEs also collaborate with internal teams to drive continuous improvement and foster strong supplier relationships.

What are the key skills and qualifications needed to thrive as a supplier quality engineer?

To thrive as a Supplier Quality Engineer, you need expertise in quality management systems, auditing, root cause analysis, and a relevant engineering degree. Familiarity with tools like Six Sigma, FMEA, ISO 9001 standards, and supplier management software is typically required, along with certifications such as ASQ CQE (Certified Quality Engineer). Exceptional communication, negotiation skills, and attention to detail help build strong supplier relationships and resolve issues efficiently. These skills ensure consistent product quality, reduce supply chain risks, and drive continuous improvement in manufacturing processes.

What are some common challenges faced by supplier quality engineers when managing multiple suppliers?

Supplier Quality Engineers often juggle the demands of overseeing multiple suppliers, each with their own processes and quality standards. A common challenge is maintaining consistent communication and ensuring that all suppliers meet the company's quality requirements and compliance standards. Additionally, they must quickly address and resolve quality issues that arise, often coordinating corrective actions across different time zones and cultures. Successful Supplier Quality Engineers rely on strong organizational skills, proactive risk management, and effective relationship-building to ensure a reliable supply chain.

What is the difference between Supplier Quality Engineering vs Quality Assurance Engineer?

AspectSupplier Quality EngineeringQuality Assurance Engineer
Primary FocusManaging supplier quality, audits, and supplier developmentEnsuring product quality through process audits and compliance
Work EnvironmentCollaborates closely with suppliers and manufacturing teamsWorks mainly within internal quality systems and production processes
CertificationsASQ CQE, ISO auditor, Six SigmaASQ CQE, ISO auditor, Six Sigma
Industry UsageCommon in manufacturing, automotive, aerospaceWidespread across manufacturing, software, and service industries

Supplier Quality Engineering focuses on managing and improving the quality of suppliers, ensuring materials meet standards before reaching production. Quality Assurance Engineers concentrate on internal processes and product quality within the organization. Both roles require similar certifications and often work together to ensure overall product quality.

How much does a supplier quality engineer make in the US?

A supplier quality engineer in the US typically earns between $70,000 and $110,000 annually, depending on experience, location, and industry. Entry-level positions may start around $60,000, while experienced professionals with certifications like ASQ may earn higher salaries. The role often requires knowledge of quality standards, inspection tools, and supplier management.

What do supplier quality engineers do?

Supplier quality engineers are responsible for ensuring that suppliers meet quality standards by conducting audits, analyzing defect data, and implementing corrective actions. They collaborate with suppliers and internal teams to improve product quality, often using tools like root cause analysis and quality management systems. Their work helps maintain product reliability and compliance with industry regulations.
More about Supplier Quality Engineering jobs

What cities are hiring for Supplier Quality Engineering jobs?

Cities with the most Supplier Quality Engineering job openings:

What are the most commonly searched types of Supplier Quality Engineering jobs?

The most popular types of Supplier Quality Engineering jobs are:

What states have the most Supplier Quality Engineering jobs?

States with the most job openings for Supplier Quality Engineering jobs include:

Infographic showing various Supplier Quality Engineering job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $73,726 per year, or $35.4 per hour.

Sr Manager, Supplier Quality Engineering

Imperative Care

Campbell, CA โ€ข On-site

Full-time

Medical, Retirement, PTO

Posted 26 days ago


Job description

SUMMARY:
Manage Supplier Quality Engineering group and Contract Manufacturing Quality in support of the manufacturing, development, and distribution of Imperative Care’s medical device products consistent with the Company’s Quality Policy and Quality Objectives.  Establish and maintain quality assurance standards that adhere to ISO 13485, FDA, and other governmental regulations within Supplier Management processes and group.
 
  • Manage and direct the collaboration with suppliers/CMs/OEMs and business partners to ensure robust materials, products, processes, and systems.
  • Manage all employee related activities, including day-to-day resourcing, hiring, mentoring and on-going development of the staff.
  • Recommends changes to policies and establishes procedures that affect section or multiple disciplines.
  • Partner with Procurement, R&D, Operations, Supply Chain and Suppliers in the timely investigation, resolution/prevention of supplier-related issues to minimize/prevent business disruptions.
  • Monitor the analysis of supplier performance metrics, identify areas of opportunity, communicate supplier risks, and drive the resolution of supplier quality issues and risk control processes.
  • Monitor and manage SCARs resolution and implementation of each SCAR, managing the SCAR age metric.
  • Managing supplier Audits/requalification process.
  • Managing the Incoming Inspection Team, process, oversee incoming inspection acceptance activities, offering direction to specify and develop component acceptance criteria/test procedures for purchased subassemblies and components.
  • Spearhead and supplier related non-conformances, including leading/participating in investigations.
  • Analyse product/components failures, metrics and deep failure analysis to offer advice in project management activities that address said failures and metrics improvement.
  • Develop, implement and monitor various quality metrics. Identify opportunities for continuous improvement and customer satisfaction. Compile and represent data for quality process reviews identifying issues/performance, or component design improvement activities.
  • Help in project management activities for a series of product, compliance and quality projects
  • Ensure compliance to regulatory requirements. Uphold quality system. Support internal and external audits.
  • Provide quality metric data to various functional groups within the organization.
  • Actively promote and support the company’s management review process.
  • Conduct Supplier qualification audits for new supplier (when is required) by planning, conducting, reporting, and follow-up on supplier quality system audits.
  • Drive and execute supplier quality agreements by working with different department within ICI and the suppliers.
  • Oversee the component qualification change projects in collaboration with key business partners and the supplier’s applicable functional groups.
  • Apply Project Management methodologies to plan, organize, connect, shape, lead, and deliver results for supplier quality management (SQM) projects.
  • Responsible for presenting supplier-related issues or opportunities to next management level.
  • Manage all departmental employee related activities, including the day-to-day resourcing, hiring, mentoring, and on-going development to the staff.
  • Manage, Train and mentor engineers, IQC Technicians and other project team members on best practices in quality engineering and regulatory compliance to external standards.
EDUCATION/EXPERIENCE:                                                                                                                                           
  • BS in Engineering or related discipline and 8+ years of supplier quality experience; or MS in Engineering with 6+ years of related experience; or equivalent combination of education and work experience in the medical device or related regulated industry Lead development and validation of test methods to comply with recognized standards
  • 2+ years of supervisory experience strongly preferred
  • Experience leading supplier or process issues (CAPAs, NCRs, SCARs, etc.)
  • Must have strong knowledge of quality system requirements (FDA 21 CFR Part 820, ISO 13485), risk management standards (ISO 14971), and good manufacturing practices.         
  • Excellent communications skills (both written and verbal)
  • Must be able to write clear, concise, and well thought out technical documentation.
  • Ability to communicate effectively, both orally and in writing, with all organizational levels
  • Strong attention to detail and ability to function in a fast-paced dynamic environment.
  • Lead auditor certification a plus

At Imperative Care, employees share in our collective success through a comprehensive rewards package that includes stock options, bonus opportunities, competitive salaries, a 401(k) plan, health benefits, generous paid time off, and a parental leave program.
Salary Range - 190,000-210,000

The salary range provided is a general guideline. When determining an offer, Imperative Care considers several factors, including the scope and responsibilities of the position, the candidate’s experience, education and training, key skills, internal equity, location, market conditions, and business needs.

Join us and help shape the future of stroke care.

The use of external recruiters/staffing agencies requires prior approval from our Human Resources Department. The Human Resources Department at Imperative Care requests that external recruiters/staffing agencies not to contact Imperative Care employees directly in an attempt to present candidates. Complying with this request will be a factor in determining future professional relationships with Imperative Care.

Imperative Care will not accept unsolicited resumes from any source other than candidates themselves for either current or future positions. Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the external recruiter/staffing agency does not create any implied obligation on the part of Imperative Care.

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