Quality Systems Engineer I – CAPA & Process Validation

Jabil; City of Elmira (NY); On-site; USD 59,000 - 94,000; Full time

Benefits offered by this job

Competitive base salary

Medical, Dental, Vision Insurance

401K match

Employee Stock Purchase Plan

Paid Time Off

Tuition Reimbursement

Life Insurance

Commuter Benefits

Employee Assistance Program

Pet Insurance

Adoption Assistance

Annual Merit Increases

Community Volunteer Opportunity

Job summary

Jabil in Elmira, NY is seeking a Quality Engineer I to develop, implement and maintain Quality System requirements across manufacturing, supplier management and process validation. The role focuses on non-conforming product handling, CAPA, calibration, supplier auditing, and sterility assurance, with emphasis on root-cause analysis and continuous improvement.

The position requires a Bachelor’s degree and at least 1 year of quality-system experience, with travel up to 10% and a commitment to

Qualifications

• Bachelor’s degree in sciences, engineering or related field.
• Experience in medical device quality systems (ISO 9001/QSR) preferred.
• Ability to manage multiple projects in a fast-paced environment.

Responsibilities

• Develop, implement and maintain Quality System requirements.
• Lead CAPA investigations and root-cause analyses.
• Conduct supplier audits and qualification.
• Design gauging and validate measurement systems.
• Review documents and drawings for manufacturing.
• Provide metrics and quality reporting.
• Support design reviews and risk analysis.

Skills

Quality systems

CAPA

Root cause analysis

Statistical methods

Calibration/measurement

Education

Bachelor’s degree in Sciences, Engineering or related field

Tools

Gage design

Design of Experiments

Statistical Process Control

Job description

Jabil in Elmira, NY is seeking a Quality Engineer I to develop, implement and maintain Quality System requirements across manufacturing, supplier management and process validation. The role focuses on non-conforming product handling, CAPA, calibration, supplier auditing, and sterility assurance, with emphasis on root-cause analysis and continuous improvement.

The position requires a Bachelor’s degree and at least 1 year of quality-system experience, with travel up to 10% and a commitment to