Supplier Quality Engineer I

Lancesoft; Englewood (CO); On-site; USD 70,000 - 90,000; Part time

Job summary

Lancesoft seeks a Supplier Quality Engineer I in Englewood, CO to support SPPA remediation and QMS integration. You will collect and analyze supplier data, identify gaps, and implement robust quality controls across supplier processes.

The role requires a Bachelor’s degree in Engineering (CQE/CRE preferred) and at least 2 years in Quality/Supplier Quality, with medical device experience strongly preferred. This is a 6-month contract based in Englewood, Colorado.

Qualifications

• Bachelor's degree in Engineering or equivalent with Quality exp; CQE/CRE preferred.
• Minimum of 2 years in Quality Engineering, Supplier Quality, or related role; medical device experience preferred.

Responsibilities

• Execute SPPA remediation activities to support Quality Management System integration.
• Gather, review, and analyze supplier manufacturing, quality, inspection, and process data to identify gaps and establish controls.
• Plan and execute remediation activities with established timelines; work cross-functionally with QA, Manufacturing, Development, and external suppliers.
• Drive remediation activities through to closure with strong communication and project execution.

Skills

Supplier quality

Process validation

Process capability

Measurement systems analysis

Inspection controls

Gage R&R

GD&T interpretation

Drawing interpretation

ISO & QSR/QMSR

Cross-functional collaboration

Education

Bachelor's degree in Engineering

CQE/CRE certification preferred

Job description

Title

Supplier Quality Engineer I

Location

Englewood, CO 80112

Duration

6 Months, End date is 04/30/2027

Duties

Responsible for executing Supplier Production Process Approval (SPPA) remediation activities in support of Quality Management System integration. Gathers, reviews, and analyzes supplier manufacturing, quality, inspection, and process data to identify gaps and establish appropriate quality controls. Plans and executes assigned supplier remediation activities against established project timelines and works cross-functionally with Supplier Quality, Manufacturing, Development, Quality, and external suppliers to drive activities through completion.

Skills

• Strong knowledge of supplier quality, process validation, process capability, measurement system analysis, and inspection controls.
• Experience evaluating manufacturing processes and quality data, including process capability studies and Gage R&R.
• Ability to interpret engineering drawings, specifications, tolerances, CTQs, and GD&T and translate technical requirements into appropriate process and inspection controls.
• Working knowledge of applicable ISO and QSR/QMSR requirements.
• Demonstrated ability to identify quality and documentation gaps, develop appropriate solutions, and drive remediation activities through closure.
• Strong analytical, problem-solving, communication, and project execution skills, with the ability to work independently and effectively with cross-functional teams and external suppliers.

Education

Bachelor s degree in Engineering or an alternative Bachelor s degree with relevant Quality Engineering experience or certification (e.G., CQE). Certification as a Quality Engineer (CQE), Reliability Engineer (CRE), or other applicable ASQ certification preferred. Minimum of 2 years of experience in a Quality Engineering, Supplier Quality, or related role, with medical device experience strongly preferred. An equivalent combination of education, certification, and relevant experience may be considered.