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Process Development Engineer ll

Abbott

Process Development Engineer ll

full-timePosted: Jan 12, 2026

Job Description

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, nutritional’s and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. 

Senior Process Development Engineer 

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 for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. 

  • An excellent retirement savings plan with a high employer contribution 

  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU 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 

Our St Paul, Minnesota location is seeking a high caliber, motivated, self-driven individual to join our Process Development engineering team for delivery catheter system development in Abbott’s Vascular business unit. This is a fully onsite role.  

What You’ll Work On 

  • Design and develop manufacturing processes, tooling, and fixtures to meet new product program schedules, enhancing product quality and taking into consideration problems inherent in the transfer of technology from research to manufacturing. 

  • Utilize methodologies and statistical analyses, such as DMAIC, Gage R&R, Cp/Cpk and SPC, to analyze and improve processes, components and products. 

  • Work with cross-functional teams including R&D, Quality, Operations, and Regulatory teams. Collaborate with R&D to ensure adherence to Design for Manufacturability (DFM) principles. 

  • Understand principles of Cost of Goods Sold (COGS) including material, direct labor, and overhead costs as well as in consideration to manufacturing process yields. 

  • Proficient in reading and creating engineering drawings, including dimensions, tolerances, and schematics.  

  • Drive process improvements and validations through manufacturing implementation and revise process failure mode effects analyses (pFMEAs). 

  • Author and execute validation protocols and reports including installation qualifications (IQ), operational qualifications (OQ), performance qualifications (PQ), and process performance qualifications (PPQ).  

  • Maintain communications with all levels of employees, customers, and vendors. 

  • Comply with U.S. Food and Drug Administration (FDA) regulatory requirements, Company policies, operating procedures, processes, and task assignments. 

  • May make recommendations concerning the acquisition and use of new technological equipment and materials. 

Required Qualifications 

  • Bachelor’s degree or an equivalent combination of education and work experience.  

  • 2+ years of related medical device experience 

  • Working technical knowledge and application of concepts, practices and procedures. 

  • General understanding of business unit/group function. 

  • Will perform this job in a quality system environment. 

  • Failure to adequately perform tasks can result in noncompliance with governmental regulations. 

  • Works on problems of moderate scope where analysis of situations or data requires a review of identifiable factors. 

  • Exercises judgment within defined procedures and practices to determine appropriate action. 

  • Has a broad knowledge of technical alternatives and an understanding of their impact on the systems environment. 

 

Preferred Qualifications 

  • Medical Device experience 

Additional Qualifications:  

•  Be innovative, resourceful, and work with minimal direction 
•  Have excellent organization, problem solving, communication, and team leadership skills 
•  Have ability to multitask, priorities their work and make data driven decisions 
•    Work effectively with cross-functional teams     

 



The base pay for this position is $61,300.00 – $122,700.00. In specific locations, the pay range may vary from the range posted.

Locations

  • St. Paul, Minnesota, United States

Salary

Estimated Salary Rangemedium confidence

75,000 - 135,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • DMAICintermediate
  • Gage R&Rintermediate
  • Cp/Cpkintermediate
  • SPCintermediate
  • Design for Manufacturability (DFM)intermediate
  • Cost of Goods Sold (COGS) analysisintermediate
  • Engineering drawingsintermediate
  • pFMEAsintermediate
  • Validation protocolsintermediate

Required Qualifications

  • Process Development engineering experience (experience)
  • Statistical analysis proficiency (experience)

Responsibilities

  • Design and develop manufacturing processes, tooling, and fixtures
  • Analyze and improve processes using statistical methodologies
  • Collaborate with cross-functional teams (R&D, Quality, Operations, Regulatory)
  • Drive process improvements and validations
  • Author and execute validation protocols and reports

Benefits

  • general: Free medical coverage (HIP PPO)
  • general: Retirement savings plan with high employer contribution
  • general: Tuition reimbursement
  • general: Freedom 2 Save student debt program
  • general: FreeU education benefit

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Abbott logo

Process Development Engineer ll

Abbott

Process Development Engineer ll

full-timePosted: Jan 12, 2026

Job Description

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, nutritional’s and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. 

Senior Process Development Engineer 

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 for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. 

  • An excellent retirement savings plan with a high employer contribution 

  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU 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 

Our St Paul, Minnesota location is seeking a high caliber, motivated, self-driven individual to join our Process Development engineering team for delivery catheter system development in Abbott’s Vascular business unit. This is a fully onsite role.  

What You’ll Work On 

  • Design and develop manufacturing processes, tooling, and fixtures to meet new product program schedules, enhancing product quality and taking into consideration problems inherent in the transfer of technology from research to manufacturing. 

  • Utilize methodologies and statistical analyses, such as DMAIC, Gage R&R, Cp/Cpk and SPC, to analyze and improve processes, components and products. 

  • Work with cross-functional teams including R&D, Quality, Operations, and Regulatory teams. Collaborate with R&D to ensure adherence to Design for Manufacturability (DFM) principles. 

  • Understand principles of Cost of Goods Sold (COGS) including material, direct labor, and overhead costs as well as in consideration to manufacturing process yields. 

  • Proficient in reading and creating engineering drawings, including dimensions, tolerances, and schematics.  

  • Drive process improvements and validations through manufacturing implementation and revise process failure mode effects analyses (pFMEAs). 

  • Author and execute validation protocols and reports including installation qualifications (IQ), operational qualifications (OQ), performance qualifications (PQ), and process performance qualifications (PPQ).  

  • Maintain communications with all levels of employees, customers, and vendors. 

  • Comply with U.S. Food and Drug Administration (FDA) regulatory requirements, Company policies, operating procedures, processes, and task assignments. 

  • May make recommendations concerning the acquisition and use of new technological equipment and materials. 

Required Qualifications 

  • Bachelor’s degree or an equivalent combination of education and work experience.  

  • 2+ years of related medical device experience 

  • Working technical knowledge and application of concepts, practices and procedures. 

  • General understanding of business unit/group function. 

  • Will perform this job in a quality system environment. 

  • Failure to adequately perform tasks can result in noncompliance with governmental regulations. 

  • Works on problems of moderate scope where analysis of situations or data requires a review of identifiable factors. 

  • Exercises judgment within defined procedures and practices to determine appropriate action. 

  • Has a broad knowledge of technical alternatives and an understanding of their impact on the systems environment. 

 

Preferred Qualifications 

  • Medical Device experience 

Additional Qualifications:  

•  Be innovative, resourceful, and work with minimal direction 
•  Have excellent organization, problem solving, communication, and team leadership skills 
•  Have ability to multitask, priorities their work and make data driven decisions 
•    Work effectively with cross-functional teams     

 



The base pay for this position is $61,300.00 – $122,700.00. In specific locations, the pay range may vary from the range posted.

Locations

  • St. Paul, Minnesota, United States

Salary

Estimated Salary Rangemedium confidence

75,000 - 135,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • DMAICintermediate
  • Gage R&Rintermediate
  • Cp/Cpkintermediate
  • SPCintermediate
  • Design for Manufacturability (DFM)intermediate
  • Cost of Goods Sold (COGS) analysisintermediate
  • Engineering drawingsintermediate
  • pFMEAsintermediate
  • Validation protocolsintermediate

Required Qualifications

  • Process Development engineering experience (experience)
  • Statistical analysis proficiency (experience)

Responsibilities

  • Design and develop manufacturing processes, tooling, and fixtures
  • Analyze and improve processes using statistical methodologies
  • Collaborate with cross-functional teams (R&D, Quality, Operations, Regulatory)
  • Drive process improvements and validations
  • Author and execute validation protocols and reports

Benefits

  • general: Free medical coverage (HIP PPO)
  • general: Retirement savings plan with high employer contribution
  • general: Tuition reimbursement
  • general: Freedom 2 Save student debt program
  • general: FreeU education benefit

Target Your Resume for "Process Development Engineer ll" , Abbott

Get personalized recommendations to optimize your resume specifically for Process Development Engineer ll. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Process Development Engineer ll" , Abbott

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score
Quiz Challenge

Answer 10 quick questions to check your fit for Process Development Engineer ll @ Abbott.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.