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Manufacturing Technician in Minnetonka

Energy Jobline ZR, Minnetonka, MN, United States


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

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

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 (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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