Quality Engineer: CAPA & Process Controls in Regulated Manufacturing

Guided Search Partners; Town of Vermont (WI); On-site; USD 75,000 - 90,000; Full time

Job summary

A professional recruitment firm is seeking a Quality Engineer to lead investigations and drive continuous improvement within a regulated manufacturing environment. The ideal candidate will have a Bachelor's degree in Engineering or Science and at least 4 years of relevant experience. Responsibilities include managing CAPA and nonconformance efforts, supporting supplier quality, and contributing to validation processes. This role offers visibility and impact on internal quality systems, providing a unique opportunity for professional growth and influence.

Qualifications

• 4+ years in medical device or similarly regulated manufacturing.
• Experience with CAPA, nonconformance, and root cause methods.
• Comfortable taking technical ownership of quality systems.

Responsibilities

• Lead investigations, validations, and process controls.
• Drive CAPA, nonconformance, and root cause efforts.
• Support supplier quality and document control activities.

Skills

Quality control

Process improvement

Cross-team collaboration

Technical communication

Education

Bachelor’s degree in Engineering or Science

Tools

ISO 13485

FDA quality controls

Job description

A professional recruitment firm is seeking a Quality Engineer to lead investigations and drive continuous improvement within a regulated manufacturing environment. The ideal candidate will have a Bachelor's degree in Engineering or Science and at least 4 years of relevant experience. Responsibilities include managing CAPA and nonconformance efforts, supporting supplier quality, and contributing to validation processes. This role offers visibility and impact on internal quality systems, providing a unique opportunity for professional growth and influence.