Manufacturing Technician in Minnetonka

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

1. st Shift: Monday – Thursday, ~5:00 AM – 3:30 PM
2. nd Shift: Monday – Thursday, ~3:30 PM – 2:00 AM
3. rd 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 #J-18808-Ljbffr Energy Jobline ZR