Process Development Engineer II

Plymouth, MN, US • Posted 18 hours ago • Updated 46 minutes ago
Full Time
On-site
Compensation information provided in the description
Fitment

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Job Details

Skills

  • PPO
  • Process Engineering
  • Process Improvement
  • Root Cause Analysis
  • ROOT
  • Design Of Experiments
  • Continuous Improvement
  • Regulatory Compliance
  • Risk Assessment
  • Quality Management
  • Collaboration
  • Research and Development
  • Supply Chain Management
  • Product Development
  • Technical Training
  • Mentorship
  • Innovation
  • IT Management
  • Mechanical Engineering
  • Biomedicine
  • Analytical Skill
  • Problem Solving
  • Conflict Resolution
  • Technical Writing
  • Documentation
  • Communication
  • Presentations
  • Manufacturing
  • Process Control
  • Medical Devices
  • ISO 13485

Summary

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You?ll also have access to:

  • Career development with an international company where you can grow the career you dream of.
  • Employees can qualify forfree medical coverage in ourHealth Investment Plan (HIP) PPOmedical plan in the next calendar year.
  • An excellent retirement savings plan with a high employer contribution
  • Tuition reimbursement, the student debt program, and education benefit - an affordable and convenient path to getting a bachelor?s degree.
  • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
  • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position works out of our Plymouth, MN location in the EP division.

In Abbott?s Electrophysiology (EP) business, we?re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.

What You?ll Work On

  • Process Development & Implementation:
    • Lead the design, development, and implementation of new manufacturing processes and equipment.
    • Specify, acquire, and validate new equipment to support production and process improvements.

  • Problem Solving & Root Cause Analysis:
    • Apply structured problem-solving methodologies to identify root causes of process issues.
    • Develop and implement corrective and preventive actions (CAPAs).

  • Data-Driven Improvements:
    • Design and execute experiments (DOE), analyze data, and present findings to cross-functional teams.
    • Drive continuous improvement initiatives to enhance product quality, reduce waste, and increase efficiency.

  • Documentation & Compliance:
    • Create and maintain technical documentation including SOPs, risk assessments, validation protocols, and safety instructions.
    • Ensure all processes comply with internal quality systems and external regulatory requirements.

  • Cross-Functional Collaboration:
    • Work closely with R&D, Quality, Manufacturing, and Supply Chain teams to support product development and scale-up.
    • Provide technical training and mentorship to technicians and junior engineers.

  • Innovation & Technical Leadership:
    • Evaluate and recommend new materials, tools, and technologies to improve manufacturing capabilities.
    • Support tooling development and process validation for new and existing products.

Required Qualifications

  • Bachelor?s degree in engineering(Mechanical, Biomedical, Chemical, or related field) with2?5+ yearsof relevant experience OR master?s degree with0?2 yearsof experience or an equivalent combination of education and experience.
  • Strong analytical and problem-solving skills.
  • Proficiency in technical writing and documentation.
  • Ability to work independently and collaboratively in cross-functional teams.
  • Excellent communication and presentation skills.
  • Working knowledge of manufacturing systems, automation, and process control.

Preferred Qualifications

  • Experience in themedical device industry, particularly withcatheter manufacturingor similar regulated environments.
  • Familiarity withGMP,ISO 13485, andFDA regulations.
  • Hands-on experience withprocess validation,DOE, andstatistical analysis.

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at , on Facebook at , and on Twitter @AbbottNews.



The base pay for this position is $68,000.00 ? $136,000.00. In specific locations, the pay range may vary from the range posted.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: appfeed
  • Position Id: 18316_31144918
  • Posted 18 hours ago
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