{"id":3711651,"url":"https://alion.io/job/freudenberg-product-development-technician-ii","title":"Product Development Technician II","company":{"id":5091,"name":"Freudenberg","domain":"freudenberg.com","url":"https://alion.io/company/freudenberg","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":76,"open_postings":171,"ghost_share":0,"stale_share":0.942,"repost_share":0,"time_to_fill_p50_days":32,"computed_at":"2026-11-08T05:47:12Z"}},"role":"Field & Service","role_family":"Field & Service","seniority":"middle","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Minnetonka, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GLP","optional":false},{"name":"GMP","optional":false}],"status":"live","first_seen_at":"2026-11-03T23:29:07Z","employer_posted_date":"2026-11-03","last_verified_at":"2026-11-08T13:36:49Z","board_verified":true,"closed_at":null,"days_open":5,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":5},"description":"Working at Freudenberg: We will wow your world!\nResponsibilities:\nIntermediate understanding of procedures.\n\nTroubleshoots basic issues.\n\nManages consumables and work area.\n\nShares knowledge with peers.\n\nReceives a moderate level of guidance and direction.\n\nProficient understanding of GMP and Good Laboratory Practices (GLP).\n\nSolid grasp of medical device development processes and regulatory requirements (e.g., FDA, ISO).\n\nStrong understanding of engineering principles and practices.\n\nAbility to read, interpret, and create technical documents, including blueprints and schematics.\n\nExperience using and maintaining hand and power tools relevant to product development.\n\nQualifications:\nExperience: 2-4 years of relevant experience in medical device manufacturing, product development, prototyping, or a similar regulated manufacturing environment.\nPrototyping & Assembly: Experience building developmental components, sub-assemblies, and prototype medical devices using precision tools, microscopes, and specialized assembly techniques.\nTest Methods: Experience supporting the development and execution of test methods, conducting product testing, and accurately recording technical data.\nDocumentation & Compliance: Working knowledge of Good Documentation Practices (GDP), manufacturing work instructions, and quality management system requirements.\nMaterials & Processes: Familiarity with materials, equipment, and manufacturing processes commonly used in medical device development and production.\nAttention to Detail: Demonstrates accuracy and precision when recording data, following procedures, and maintaining quality standards.\nCross-Functional Communication: Ability to communicate effectively and work with R&D, Quality, Regulatory, Manufacturing, and other cross-functional teams.\nProblem-Solving & Flexibility: Ability to troubleshoot assembly, testing, and process issues while adapting to changing priorities in a regulated environment.\n \nThe Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. 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