{"id":167809,"url":"https://alion.io/job/novanta-quality-engineer","title":"Quality Engineer","company":{"id":58917,"name":"Novanta","domain":"novanta.com","url":"https://alion.io/company/novanta","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":82,"open_postings":13,"ghost_share":0,"stale_share":0.692,"repost_share":0.077,"time_to_fill_p50_days":43,"computed_at":"2026-11-04T06:34:25Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":null,"employment_type":"full_time","work_mode":"hybrid","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Přelouč, Czech Republic"],"countries":["CZ"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":23000,"max_usd":54000,"period":"year","method":"role_country_seniority_unknown","sample_n":62},"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"FMEA","optional":false},{"name":"GMP","optional":false},{"name":"ISO 13485","optional":false}],"status":"live","first_seen_at":"2026-07-23T00:00:00Z","employer_posted_date":"2026-07-23","last_verified_at":"2026-11-04T05:46:22Z","board_verified":true,"closed_at":null,"days_open":104,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":104},"description":"Build a career powered by innovations that matter! At Novanta, our innovations power technology products that are transforming healthcare and advanced manufacturing-improving productivity, enhancing people’s lives and redefining what’s possible. We create for our global customers engineered components and sub-systems that deliver extreme precision and performance for a range of mission-critical applications-from minimally invasive surgery to robotics to 3D metal printing.\nNovanta is one global team with over 26 offices located in The Americas, Europe and Asia-Pacific. Looking for a great place to work? You have found it with a culture that embraces teamwork, collaboration and empowerment. Come explore Novanta.\nPrimary Responsibilities\nLead and coordinate quality and validation activities related to production transfers and manufacturing changes.\n\nCreate, review, approve validation documentation including plan / protocols, reports, process control plan and associated controlled documentation.\n\nParticipate in process, equipment and manufacturing validations and ensure compliance with applicable quality and regulatory requirements.\n\nTo ensure that validation activities are appropriately planned, executed, and documented to maintain compliance of manufacturing processes, equipment, and associated documentation within controlled manufacturing and cleanroom environments.\n\nParticipate in transfers of products and manufacturing processes between Novanta sites from a quality and validation perspective.\n\nCollaborate closely with Project Management, Regulatory Affairs, Operations and Quality teams to ensure successful implementation of changes.\n\nCreate, review, approve risk management documentation (PFMEA).\n\nEvaluate impact of manufacturing changes to validation status and support implementation activities.\n\nSupport internal, customer and certification audits.\n\nSupport root cause investigations and continuous improvement activities using appropriate quality tools\n\nRequired Experience, Education, Skills, Training and Competencies\nExperience working in a regulated manufacturing environment such as medical devices, pharmaceuticals, biotechnology, food supplements or similar industries\n\nHands-on experience with validation activities and controlled documentation\n\nKnowledge of quality standards and regulations (ISO 13485, ISO 9001, GMP or similar)\n\nExperience working in cleanroom or controlled manufacturing environments is highly desirable\n\nAbility to work independently while collaborating effectively within cross-functional teams\n\nStrong documentation and communication skills\n\nFluent Czech and English\n\nWhat we offer\nThe opportunity to work for a stable international company developing and manufacturing medical devices\n\nThe chance to contribute to international projects and collaborate with colleagues across global sites\n\nFlexible working hours\n\nHybrid working model with up to 2 days of home office per week\n\n25 days of annual leave\n\nFree lunches\n\nCompany contribution to pension savings\n\nEdenred benefits card\n\nTransportation allowance\n\nEmployee referral bonus\n\nAnnual salary review based on performance\n\nNovanta is proud to be an equal employment opportunity and affirmative action workplace. 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