Job Description

Manufacturing Process Technician (Electrophysiology) – Minnetonka, MN

Position Overview

This role is based in Abbott’s Electrophysiology (EP) business in Minnetonka, MN. The Manufacturing Process Technician will support a new product launch by working closely with the Operations team, including assemblers, to troubleshoot equipment and investigate process issues.

This position plays a key role in designing and developing manufacturing processes, tooling, and fixtures to meet production schedules while improving productivity and product quality. It offers a unique opportunity to contribute to a state-of-the-art product and make a meaningful impact on the organization.

Key Responsibilities

• Serve as a front-line process technician supporting the Operations team
• Support new product introductions, production equipment, process improvements, and cost reduction initiatives
• Apply lean manufacturing principles and coach assemblers on best practices
• Train and instruct production personnel on manufacturing and testing procedures
• Recommend and implement improvements to processes, tooling, and equipment to enhance safety, quality, delivery, and cost
• Analyze test data and product performance to support yield improvement initiatives
• Assist maintenance in ensuring continuous operation of production equipment
• Support engineers in troubleshooting safety, quality, and process issues
• Perform scrap analysis and assist with root cause investigations
• Communicate production and process updates across shifts and teams

Qualifications

Required

• High school diploma, trade school certification, or equivalent training in Electronics, Engineering Technology, or related field
• 1–4 years of manufacturing technician experience or equivalent technical education
• Ability to work both independently and within a team in a fast-paced environment
• Strong communication skills with the ability to collaborate across functions
• Ability to train and coach non-technical personnel
• Strong organizational skills and attention to detail
• Results-oriented with the ability to manage multiple priorities
• Ability to maintain regular and reliable attendance

Preferred

• Experience in the medical device industry

Work Environment & Expectations

• Must be adaptable, resourceful, and able to work with minimal direction
• Comfortable collaborating with cross-functional teams
• Committed to supporting company initiatives and regulatory requirements, including:
• Quality Management Systems (QMS)
• Environmental Management Systems (EMS)
• FDA regulations and company policies

Shift Options

• 1st Shift: Monday – Thursday, ~5:00 AM – 3:30 PM
• 2nd Shift: Monday – Thursday, ~3:30 PM – 2:00 AM
• 3rd Shift: Friday – Sunday, ~5:00 AM – 5:30 PM

Note: Shift times may vary based on operational needs.

• Flexibility to support overtime or cross-shift coverage is strongly preferred (but not required)

Why Join This Role?

• Be part of a new product launch
• Work on cutting-edge medical technology
• Directly impact manufacturing performance and product quality
• Gain exposure to cross-functional engineering and operations teams

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