{"id":2870857,"url":"https://alion.io/job/freudenberg-sr-quality-technician","title":"Sr Quality Technician","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":80,"open_postings":176,"ghost_share":0,"stale_share":0.994,"repost_share":0,"time_to_fill_p50_days":20,"computed_at":"2026-10-22T06:10:10Z"}},"role":"Field & Service","role_family":"Field & Service","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Jeffersonville, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":51000,"max_usd":100000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":3331},"experience_years_min":3,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false},{"name":"Mandiant capa","optional":false}],"status":"live","first_seen_at":"2026-10-19T19:36:04Z","employer_posted_date":"2026-10-19","last_verified_at":"2026-10-22T13:51:24Z","board_verified":true,"closed_at":null,"days_open":2,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":2},"description":"Working at Freudenberg: We will wow your world!\nResponsibilities:\nAdvanced understanding of procedures and equipment.\n\nResolves most issues independently.\n\nPrioritizes tasks and supports training.\n\nLeads by example and formally trains junior staff or acts as a resource for colleagues with less experience.\n\nProficient in applying FDA regulations (21 CFR Part 820), ISO 13485, and other relevant standards.\n\nStrong understanding of GMP principles and quality assurance practices.\n\nSkilled in product testing, inspection, and statistical quality control.\n\nProficient in risk management methodologies and post-market surveillance.\n\nAbility to lead CAPA investigations and implement sustainable corrective actions.\n\nFamiliarity with design control processes to ensure compliance with performance criteria.\n\nParticipation in internal and external audits.\n\nQualifications:\n3-5+ years of experience in the medical device industry, including at least 3 years in Quality Engineering or Quality Systems.\nProven experience with nonconformance management, CAPA, root cause analysis, and product quality.\nBachelor’s degree in Engineering, Quality, Biomedical Engineering, or a related technical field preferred will take experience in lieu of degree \nExperience working within a regulated manufacturing environment.\nStrong working knowledge of medical device quality and regulatory requirements, including: FDA Quality System requirements ISO 13485 EU Medical Device Regulation (EU MDR) Good Manufacturing Practices (GMP)\nUnderstanding of quality system requirements and industry best practices.\nExperience managing and investigating nonconformances.\nExperience leading CAPA activities and root cause investigations.\nExperience with process validation and manufacturing process controls.\nExperience with change control and change management.\nExperience with software validation, as applicable.\nAbility to analyze quality data, identify trends, and drive corrective and preventive actions.\nExperience partnering with Manufacturing, Engineering, Operations, and other cross-functional teams to resolve quality issues.\n \nThe Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. 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