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Description

Performs engineering activities to support manufacturing of commercial and non-commercial finished medical devices. Primary responsibility for this role will be supporting maturation and stabilization for a newly launched Neurovascular device. Investigates and resolves daily production issues involving equipment and process. Identifies opportunities to improve cost, yield and process efficiencies and turns ideas into realization. Performs validation activities associated with process or material changes. Exercises independent judgment in planning and organizing work; monitors performance and reports status. Provides technical information to development teams concerning manufacturing or processing techniques, materials, properties and process (advantages/limitations) engineering planning.

Skills

Manufacturing engineering, Process engineering, Medical device, Process improvement, Manufacturing process, Continuous improvement, Lean manufacturing, Six sigma, equipment maintenance, equipment validation, material control, quality control, troubleshooting, Validation, supply chain processes

Additional Skills & Qualifications

Essential Duties and Responsibilities (but are not limited to):

Provides daily support of products, processes, materials, and equipment to achieve production goals.

Build Quality into all aspects of their work by maintaining compliance to all quality requirements.

Troubleshoot, repair, qualify or validate new and existing equipment used to manufacture endovascular catheters.

Prepare testing and justification to support process, equipment and material changes.

Determine appropriate level of testing required per internal procedures, customer alignment and regulatory acceptance requirements provided.

Work with purchasing to optimize supply chains, recommend projects which reduce risk and/or reduce cost, and develop long-term commodity strategies.

Design, implement and monitor Statistical Process Monitoring system

Monitors daily yields and acts immediately to investigate and resolve issues to meet scrap and output goals.

Designs, procures, and fabricates equipment tooling and fixtures.

Performs troubleshooting on existing products/process problems as related to design, material, or processes.

Prepares validation protocols and reports to communicate results and conclusions.

May lead cross-functional project teams.

Identifies, implements, and manages equipment, labor and cycle time requirements to support production goals.

Trains and/or provides work direction to operators/technicians.

May perform or support TMV’s.

Identify/Investigate Manufacturing issues (non-conformances) with root cause analysis and disposition production material through NCMR Process.

Responsible for notifying QA/QC of any observed or reported product quality issues so that appropriate action may be taken.

Technical Skills:

Experience in medical device manufacturing.

Familiar with catheter product design, manufacturing processes and applications.

Summarizes, analyzes, and draws conclusions from test results.

Highly proficient with MS Office (Word, Excel, Access, Project and PowerPoint), internet an

Job Type & Location

This is a Contract to Hire position based out of Brooklyn Park, MN.

Pay and Benefits

The pay range for this position is $43.00 - $62.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Brooklyn Park,MN.

Application Deadline

This position is anticipated to close on Dec 5, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

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 [email protected] (%[email protected]) for other accommodation options.