Quality Engineer: Med Devices Process & Compliance

Abbott; Temecula (CA); On-site; USD 61,000 - 123,000; Full time

Benefits offered by this job

Career development

Health coverage

Retirement plan

Job summary

Abbott Vascular in Temecula, CA is seeking a Quality Engineer to provide process/quality engineering support on the manufacturing line and with product development teams. The role emphasizes CAPA execution, audits, and aligning processes with FDA and industry standards.

You will lead cross-functional initiatives, ensure documentation quality, and drive improvements in quality tools and systems. Onsite work with collaboration across Abbott stakeholders.

Qualifications

• Bachelor's degree in Engineering or Life Sciences required
• 2–5+ years related work experience in quality/engineering functions preferred
• Experience with CAPA, audits, and quality systems is desirable

Responsibilities

• Support manufacturing line with process/quality engineering activities
• Assist with internal and external audits and CAPA closure
• Improve processes to meet regulatory and customer requirements
• Lead or participate in cross-functional project teams
• Ensure timely documentation according to business standards
• Serve as SME on technical matters and interface with external partners

Skills

CAPA experience

Problem solving

Documentation

Quality systems

Education

Bachelor's degree in Engineering/Life Sciences

Job description

Abbott Vascular in Temecula, CA is seeking a Quality Engineer to provide process/quality engineering support on the manufacturing line and with product development teams. The role emphasizes CAPA execution, audits, and aligning processes with FDA and industry standards.

You will lead cross-functional initiatives, ensure documentation quality, and drive improvements in quality tools and systems. Onsite work with collaboration across Abbott stakeholders.