Medical Device Development Technician II

Freudenberg Medical, LLC; Minnetonka (MN); On-site; USD 36,000 - 47,000; Full time

Benefits offered by this job

401K Match

Diversity & Inclusion

Sustainability

Personal Development

Safe Environment

Job summary

Freudenberg Medical LLC in Minnetonka, MN is seeking a Product Development Technician II to support medical device development and prototyping in a regulated environment. This on-site role requires hands-on work with precision tools, documentation, and cross-functional collaboration.

Responsibilities include understanding procedures, troubleshooting, managing consumables, and sharing knowledge with peers while adhering to GMP/GLP standards and regulatory requirements for medical devices.

Qualifications

• 2–4 years of relevant experience in medical device manufacturing or prototyping.
• Experience building developmental components and prototypes using precision tools.
• Experience supporting the development and execution of test methods, and recording technical data.
• Knowledge of GDP and GDP-like documentation requirements and manufacturing work instructions.
• Familiarity with medical device materials, processes and regulatory considerations.

Responsibilities

• Understand procedures and troubleshoot basic issues.
• Manage consumables and the work area with a focus on cleanliness and organization.
• Share knowledge with peers to improve manufacturing practices.
• Receive guidance while maintaining hands-on involvement in tasks.
• Ensure compliance with GMP/GLP and regulatory requirements.

Skills

Attention to Detail

Cross-Functional Communication

Problem-Solving

Reading Technical Documents

Tools

Microscopes

Precision Tools

Job description

Freudenberg Medical LLC in Minnetonka, MN is seeking a Product Development Technician II to support medical device development and prototyping in a regulated environment. This on-site role requires hands-on work with precision tools, documentation, and cross-functional collaboration.

Responsibilities include understanding procedures, troubleshooting, managing consumables, and sharing knowledge with peers while adhering to GMP/GLP standards and regulatory requirements for medical devices.