{"id":1187496,"url":"https://alion.io/job/getinge-sr-quality-engineer-ops-wayne-nj","title":"Sr. Quality Engineer, Ops (Wayne, NJ)","company":{"id":719311,"name":"Getinge","domain":"getinge.com","url":"https://alion.io/company/getinge-2","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"SuccessFactors","truth_index":null},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"senior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Wayne, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":86000,"max_usd":163000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":2148},"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false},{"name":"Microsoft Office","optional":true}],"status":"live","first_seen_at":"2026-09-05T02:00:00Z","employer_posted_date":"2026-09-05","last_verified_at":"2026-09-25T03:28:17Z","board_verified":false,"closed_at":null,"days_open":22,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":22},"description":"With a passion for life\nJoin our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers.\nAre you looking for an inspiring career? You just found it.\nJob Overview\nThe Senior Quality Engineer is responsible for implementation and execution of Quality Engineering functions, ensuring the effective establishment and maintenance of quality systems.\nJob Responsibilities and Essential Duties\nLeads quality planning by ensuring assigned quality plans and necessary gap assessment are documented, effective, and completed on time. \nLeads Quality management activities, which includes ensuring that corrective and preventive actions are issued as required, properly investigated, documented, effective, and completed on time. \nRun the Material Review Board Meeting by providing and/or reviewing data to be presented for escalations of non-conforming material records. \nSupports Supplier management, which includes non-conforming material review and supporting incoming material inspection. \nCoordinates technical activities regarding validations: including protocol development, synchronization of interdepartmental activities, evaluation, and reporting results. \nLeads communications, interacts, and coordinates quality improvement efforts with Manufacturing, QA, R&D, and engineering management regarding product status, deviations, and problems; provides testing and training support to Manufacturing, Engineering and R&D \nReviews and approves product/process qualification/validation and other change control related documentation. \nIdentifies and leads implementation of new opportunities for improvements to work processes, production, QA testing, and other areas as identified. \nInvestigates product issues by conducting failure investigations within the NCMR process. \nFacilitates the investigation of component issues with Engineering, as needed. \nSupport the Health and Hazard Evaluation process by gathering required data and performing in-depth analysis prior to sharing the information with the Field Action Committee\nLead and support CAPA related activities. \nProvide mentorship and guidance to new Engineers/Interns within the organization. \nRequired Knowledge, Skills, and Abilities\nBachelor’s degree in engineering, Science or equivalent is required. A Master of Science in Engineering, Science or equivalent is preferred. CQE (Certified Quality Engineer) or CQA (Certified Quality Auditor) is desirable. \nA minimum of five years’ experience in quality assurance, quality engineering or related functions or a M.S. plus 3 years’ experience is required. Prior experience in an FDA regulated industry or ISO certified organization \nMust have demonstrated proficiency in statistical analysis, the ability to analyze and solve complex problems, and the ability to communicate effectively across departments. \nWorking knowledge of quality systems is required. Familiarity with analytical software applications is preferred. \nProject management and leadership experience is required. Previous experience supervising technicians and conducting and participating in FDA/customer/corporate audits is preferred. \nMust demonstrate effective influencing and change management skills and demonstrated achievements in process improvements. \nKnowledge of Microsoft Office Products such as Word, Excel or equivalent software applications \nThe base salary for the position is a minimum of $115, 000 and a maximum of 120,000 plus an annual bonus of 10%\n#LI-LG1\nAbout us\nWith a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.\nReasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.","description_format":"text","description_chars":4332,"description_truncated":false,"requirements":{"experience_years_min":5,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":true},"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Cardiovascular Devices","Hospital Equipment & Furniture","Sterilization & Infection Control"],"lifecycle":[{"event":"open","at":"2026-09-24T15:08:33Z"}],"liveness":{"score":59,"band":"ok","label":"Likely open","p_open":1,"p_active":0.78,"p_room":0.75,"age_days":21,"expected_fill_days":23,"reasons":["conf:26","velocity","win:late","comp:brand"],"computed_at":"2026-09-26T05:45:00Z"},"pay":null,"html_url":"https://alion.io/job/getinge-sr-quality-engineer-ops-wayne-nj","json_url":"https://alion.io/job/getinge-sr-quality-engineer-ops-wayne-nj.json","meta":{"generated_at":"2026-09-27T03:35:02Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","usage":{"tier":"crawler","counted_by":"address","units_charged":1,"used_today":3363,"day_limit":5000,"remaining_today":1637,"minute_limit":60,"resets_at":"2026-09-28T00:00:00Z"}}}