Senior Med‑Device Process Engineer — Innovate & Scale

Abbott; United States; On-site; USD 94,000 - 156,000; Full time

Benefits offered by this job

Career development

Free HIP PPO medical coverage

High employer retirement contribution

Job summary

Abbott in Temecula, CA, is seeking a Manufacturing Process Engineer to develop and optimize manufacturing processes and equipment for medical devices. You will work within Abbott Vascular, delivering compliant processes and participating in cross-functional design reviews.

The role emphasizes strong engineering fundamentals, experience with design controls, and collaboration across teams to meet time-to-market goals in an FDA-regulated environment.

Qualifications

• Bachelor's Degree in Engineering/Technical discipline (Mechanical, Chemical, Electrical or Physics).
• Master's Degree ideal.
• Minimum 4 years of relevant engineering experience.
• Solid knowledge of general engineering principles.
• Strong knowledge of design controls and medical device regulations (ISO13485, FDA).

Responsibilities

• Specify, design, verify and validate new manufacturing processes and equipment per medical regulatory standards.
• Troubleshoot process equipment and optimize processes.
• Develop process/product specifications, perform PFMEAs, DOEs, validation protocols/reports.
• Collaborate with cross-functional teams on development efforts.
• Write and issue Engineering Change Orders and maintain quality system effectiveness.

Skills

Strong engineering principles

Cross-functional collaboration

Excellent written and verbal skills

Education

Bachelor's Degree in Engineering/Technical

Master's Degree ideal

Tools

GxP / FDA knowledge

Job description

Abbott in Temecula, CA, is seeking a Manufacturing Process Engineer to develop and optimize manufacturing processes and equipment for medical devices. You will work within Abbott Vascular, delivering compliant processes and participating in cross-functional design reviews.

The role emphasizes strong engineering fundamentals, experience with design controls, and collaboration across teams to meet time-to-market goals in an FDA-regulated environment.