Manufacturing Engineer II

2 weeks ago


Saint Paul, Minnesota, United States Abbott Laboratories Full time
Job Summary

We are seeking a highly skilled Manufacturing Engineer II to join our Structural Heart Medical Device Team at Abbott Laboratories. As a key member of our engineering team, you will play a crucial role in designing and developing manufacturing processes, tooling, and fixtures to meet daily production schedules.

About Abbott

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.

Key Responsibilities

As a Manufacturing Engineer II, you will:
  • Support the operations team as a front-line engineer working with assemblers and troubleshooting equipment and process issues.
  • Manage projects aimed towards designing and developing manufacturing processes, tooling, and fixtures to meet daily production schedules, while enhancing productivity and product quality.
  • Run design of experiments studies to characterize processes to improve yield and efficiency.
  • Coach, mentor, and provide guidance to other engineers and technicians.
  • Conduct process FMEAs and process validations.
  • Improve product quality, labor efficiency, and throughput through the use of Lean manufacturing concepts.
  • Coordinate the design, procurement, build, and debug of tooling, machinery, and test equipment.
  • Work with Product Development to ensure design for manufacture.
  • Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
  • Ensure compliance with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments.

Requirements

To be considered for this role, you should have a Bachelor's Degree in Chemical, Industrial, or Mechanical Engineering, or other related discipline, and 3+ years manufacturing engineering experience in medical device or related industry, including working on and documenting process improvement initiatives. Strong verbal and written communications, analytical, problem-solving, and project management skills are also essential. Proficiency with MS Office (Word, Excel, Outlook, PowerPoint) and ability to travel approximately 10% are also required. Preferred qualifications include an advanced technical degree, medical device experience, previous transcatheter tissue heart valve experience, and Lean 6 Sigma Black Belt certification.

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