Medical Device Quality Engineer II

Jabil; Maple Grove (MN); On-site; USD 69,000 - 124,000; Full time

Benefits offered by this job

Medical, Dental, Vision Insurance

401K match

Paid Time Off

Tuition Reimbursement

Life Insurance

Commuter Benefits

Employee Assistance Program

Pet Insurance

Annual Merit Increases

Volunteer Opportunity

Job summary

Jabil is seeking a Quality Engineer II to ensure product quality and process compliance for medical device manufacturing. You will apply engineering principles to drive continuous improvement and uphold robust quality systems across operations.

Responsibilities include developing QC plans, performing CAPA, conducting data analysis, participating in design reviews, and leading supplier quality audits. Ideal candidates have a Engineering degree and 2+ years in regulated manufacturing with SPC/MSA

Qualifications

• Requires a Bachelor’s degree in Engineering and 2+ years in a regulated quality role within manufacturing.
• Proficiency in SPC, MSA and quality tools; familiarity with ISO 9001, ISO 13485, IATF 16949.

Responsibilities

• Develop, implement and maintain quality control plans for new and existing products.
• Perform root cause analysis and implement CAPA for quality issues.
• Analyze data statistically to identify trends and validate processes.
• Support design reviews with quality input.
• Lead supplier quality activities including audits and monitoring.
• Participate in internal and external audits to ensure compliance with quality standards.
• Collaborate with R&D, manufacturing, and supply chain to resolve quality issues.
• Mentor junior quality personnel on methodologies and procedures.
• Develop and implement MSA studies and measurement systems.
• Prepare and present quality performance reports to management.

Skills

SPC

MSA

CAPA

Root Cause Analysis

8D

Fishbone diagrams

Education

Bachelor's degree in Engineering

Tools

Microsoft Excel

Job description

Jabil is seeking a Quality Engineer II to ensure product quality and process compliance for medical device manufacturing. You will apply engineering principles to drive continuous improvement and uphold robust quality systems across operations.

Responsibilities include developing QC plans, performing CAPA, conducting data analysis, participating in design reviews, and leading supplier quality audits. Ideal candidates have a Engineering degree and 2+ years in regulated manufacturing with SPC/MSA