Manufacturing Engineer

Job Description

As a Manufacturing Engineer II, you will lead the manufacturing processes and drive improvements to meet cost, manufacturability, and quality goals. Your role will involve planning, designing, developing, and maintaining programs, training, and manufacturing processes such as machining, packaging, welding, assembly, and molding. You will also provide direction and support for existing products to optimize processes and ensure production goals are achieved.

• Initiate and complete technical activities leading to new or improved processes for current and next-generation programs to meet strategic goals.
• Analyze and solve complex engineering problems using novel and innovative approaches.
• Interface with quality and manufacturing teams to integrate new products or processes into existing production areas.
• Maintain and approve device routers and bill of materials.
• Monitor equipment performance, addressing issues that lead to non-conforming products or quality issues.
• Design and coordinate fabrication and implementation of process fixturing or gauging.
• Resolve non-conformances and participate in the Material Review Board.
• Analyze and map processes, assess efficiency, and implement complex project activities.
• Assist with part cost estimation.
• Support and comply with company Quality System, ISO, and medical device requirements.
• Read, understand, and follow work instructions and standard work.

• 3 years of experience in a machine shop environment.
• Experience in the medical device industry.
• Expertise in process/continuous improvement, process engineering, and manufacturing processes.
• Proficiency in Lean manufacturing, Six Sigma, Solidworks, tooling, machining, validation, and process design.
• Knowledge of manufacturing equipment, gage R&R, fixture design, ISO standards, DOE, SPC, FMEA, GMP, Unigraphics, and ProE.

• Bachelor’s Degree in Mechanical, Industrial, or other Engineering Science.
• 3 years of engineering experience in a manufacturing setting, including state-of-the-art manufacturing technology and cost reductions.
• Experience in manufacturing process design and validation.
• Expertise in manufacturing equipment and fixture/gauge design.
• Experience in an ISO
  13485/GMP environment.
• Engineering experience with medical devices.
• Lean manufacturing experience.
• Knowledge of materials and related processes.
• Project management experience.
• Experience with DOE, SPC, FMEA, GMP, QSR.
• Manufacturing automation experience, including electronic visual inspection.
• Proficiency in 3D CAD software (e.g., ProE, Unigraphics, Solidworks).

This is a Permanent position based out of Anoka, MN.

The pay range for this position is $90,000.00 – $/yr. Benefits include medical, dental, vision and life insurance options. Company also offers a 401(k) retirement plan with employer match, profit sharing, short- and long-term disability insurance, paid time off, holiday pay, and an onsite medical clinic.

Additional benefits:
Onsite Clinic, Paid Parental Leave, Monthly Social Events, Annual Employee Appreciation Week, Volunteer Opportunities, Training and Development Opportunities, Tuition Reimbursement, Wellness Program.

This is a fully onsite position in Anoka, MN.

This position is anticipated to close on Jan 19, 2026.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.