CRM Catheter Manufacturing Engineering Lead

Abbott (abbottcareers2 board)

United States

On-site

USD 90,000 - 120,000

Full time

7 days ago
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Benefits offered by this job

Tuition assistance
Paid time off
401(k) match
Health care plan
Career development

Job summary

Abbott Minnetonka is seeking a Manufacturing Engineering Supervisor to lead CRM catheter manufacturing in a regulated medical device setting. You will drive daily engineering support, ensure process stability, and lead continuous improvement initiatives.

The role focuses on line issues, CAPA, and cross-functional collaboration to meet quality and production goals in a fast-paced environment.

Qualifications

  • Bachelor's degree in Engineering required.
  • 5+ years of experience in manufacturing engineering within medical devices or regulated environments.
  • Experience supporting complex assemblies or catheter-based device manufacturing.
  • Demonstrated leadership capability (team lead, project lead, or supervisor).

Responsibilities

  • Lead, coach, and develop a team of engineers/technicians supporting CRM catheter manufacturing.
  • Prioritize and assign engineering work to meet production, quality, and capacity goals.
  • Oversee process ownership, documentation, validations (IQ/OQ/PQ), and change control.
  • Provide hands-on support for line issues, root-cause investigations, and CAPA activities.
  • Analyze process data (yield, scrap, SPC, CPK) to improve performance and reduce variation.
  • Drive continuous improvement, automation, tooling, and process optimization projects.
  • Ensure all engineering activities comply with FDA QSR, ISO 13485, and Abbott procedures.
  • Collaborate with Operations, Quality, R&D, and Supply Chain to support product and business objectives.

Skills

Leadership
Manufacturing engineering
Regulatory compliance
Problem solving

Education

Bachelor's degree in Engineering

Job description

Abbott Minnetonka is seeking a Manufacturing Engineering Supervisor to lead CRM catheter manufacturing in a regulated medical device setting. You will drive daily engineering support, ensure process stability, and lead continuous improvement initiatives.

The role focuses on line issues, CAPA, and cross-functional collaboration to meet quality and production goals in a fast-paced environment.

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