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
