Senior Process Development Engineer - Medical Devices

Thornton Tomasetti; Saint Paul (MN); On-site; USD 78,000 - 156,000; Full time

Benefits offered by this job

Career development

Medical coverage

Retirement plan

Tuition reimbursement

FreeU education

Job summary

Abbott in St. Paul, MN is seeking a Manufacturing Process Development Specialist to design and develop manufacturing processes for life sciences products.

You will work within the Vascular Devices division, contributing to transfer of technology from research to manufacturing. The role requires 4+ years of engineering experience, strong knowledge of design controls, and proven ability to operate in an FDA-regulated environment with GxP understanding.

Qualifications

• Bachelor's degree in Engineering/Technical discipline (Mechanical, Chemical, Electrical or Physics preferred) or an equivalent combination of education and work experience.
• Master's Degree (± 18 years).
• Minimum 4 years relevant experience.
• Solid knowledge of general engineering principles.
• Good knowledge of design controls and regulations for medical device development (ISO134851, ISO13485, FDA).
• Experience in development in FDA-regulated environments with GxP understanding.

Responsibilities

• Designs and develops manufacturing processes for life sciences products.
• Develops procedures for economical mass production with pilot-plant and production departments.
• Conducts tests and measurements to control variables.
• Troubleshoots production process problems with existing equipment.

Skills

Mechanical engineering

Chemical engineering

Electrical engineering

Physics

Education

Bachelor's degree in Engineering/Technical discipline

Master's degree

Tools

Statistical analysis

Tolerance analysis

Job description

Abbott in St. Paul, MN is seeking a Manufacturing Process Development Specialist to design and develop manufacturing processes for life sciences products.

You will work within the Vascular Devices division, contributing to transfer of technology from research to manufacturing. The role requires 4+ years of engineering experience, strong knowledge of design controls, and proven ability to operate in an FDA-regulated environment with GxP understanding.