Quality Engineer - 2nd Shift, Medical Devices

Thornton Tomasetti; Temecula (CA); Hybrid; USD 61,000 - 123,000; Full time

Job summary

Abbott is seeking a Quality Engineer for the 2nd shift in our Vascular division in Temecula, California. This fully onsite role supports manufacturing and product development to ensure the highest quality of patient care.

You will develop quality plans, analyze data, and lead process improvements including CAPA, FMEA, and risk analyses, collaborating across teams to deliver compliant, robust products. The position requires a Bachelor’s degree with 2–5 years of experience; CQE certification is a

Qualifications

• Bachelor's degree plus 2-5 years of related work experience with a good understanding of the specified functional area, or Master's degree with 0-2 years of related work experience, or an equivalent combination of education and work experience.
• CAPA experience
• Data Analysis experience
• Risk Management experience
• CQE Certification is a plus, Medical Devices experience preferred

Responsibilities

• Ensure compliance with applicable corporate and divisional policies and procedures.
• Identify and control manufacturing process defects by working in root-cause and CAPA teams.
• Query and bound data to support release criteria and documentation.
• Develop product quality plans, specifications, and quality systems with teams.
• Create risk analyses and FMEAs as needed.
• Develop process monitoring systems to reduce variation and defects.
• Lead process improvement to capture quality metrics and drive sustained product design and development.
• Assist in creating quality tools and training materials and evaluate their effectiveness.

Skills

CAPA experience

Data Analysis

Risk Management

Education

Bachelor's degree in related field

Master's degree (optional)

Job description

Abbott is seeking a Quality Engineer for the 2nd shift in our Vascular division in Temecula, California. This fully onsite role supports manufacturing and product development to ensure the highest quality of patient care.

You will develop quality plans, analyze data, and lead process improvements including CAPA, FMEA, and risk analyses, collaborating across teams to deliver compliant, robust products. The position requires a Bachelor’s degree with 2–5 years of experience; CQE certification is a