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Minnetonka, Minnesota, United States
Onsite
Working at Freudenberg: We will wow your world!
Intermediate understanding of procedures.
Troubleshoots basic issues.
Manages consumables and work area.
Shares knowledge with peers.
Receives a moderate level of guidance and direction.
Proficient understanding of GMP and Good Laboratory Practices (GLP).
Solid grasp of medical device development processes and regulatory requirements (e.g., FDA, ISO).
Strong understanding of engineering principles and practices.
Ability to read, interpret, and create technical documents, including blueprints and schematics.
Experience using and maintaining hand and power tools relevant to product development.
The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.
Freudenberg Medical LLC