Manufacturing Process Engineer

Abbott

Menlo Park, California, United States
Base: $81,500.00 – $141,300.00; bonus/equity: not ...
Onsite
Root cause analysis and problem solving
Design for manufacturability principles
Fda regulations and quality control compliance
Abbott is seeking a Manufacturing Process Engineer for its Menlo Park, California location, aimed at supporting the development of innovative medical devices in the Structural Heart division. The ideal candidate will possess engineering expertise, a strong background in problem-solving, and a collaborative mindset to work with cross-functional teams

Job Summary

  • This position supports the Structural Heart Business mission to restore health by designing and providing device solutions for structural heart disease.
  • The role involves investigating and resolving problems involving techniques, materials, equipment, and systems while applying multidisciplinary engineering knowledge.
  • Employees qualify for free medical coverage, a high employer contribution retirement plan, tuition reimbursement, and access to an affordable bachelor's degree program.

Matching Summary

Match Score: 85

Abbott is seeking a Manufacturing Process Engineer for its Menlo Park, California location, aimed at supporting the development of innovative medical devices in the Structural Heart division. The ideal candidate will possess engineering expertise, a strong background in problem-solving, and a collaborative mindset to work with cross-functional teams.

Salary

Base: $81,500.00 – $141,300.00; Bonus/Equity: Not specified; Benefits: Free medical coverage, retirement savings plan, tuition reimbursement

Skills & Requirements

Must-have

  • Root cause analysis and problem solving
  • Design for manufacturability principles
  • FDA regulations and Quality Control compliance
  • Cross-functional team collaboration
  • Process validation and equipment evaluation

Nice-to-have

  • Innovative medical device design experience
  • Cost-efficient business practice implementation
  • Strong communication with non-technical stakeholders
  • Knowledge of IP issues in manufacturing
  • Continuous quality improvement mindset

Key Requirements

  • Bachelor's Degree in Engineering or related field
  • Minimum 5 years of relevant work experience
  • Compliance with FDA regulations and QMS requirements

Work Rights

Not specified

Tailored Resume

Cover Letter