{"id":2821754,"url":"https://alion.io/job/jabil-supplier-quality-engineer-2","title":"Supplier Quality Engineer","company":{"id":87,"name":"Jabil","domain":"jabil.com","url":"https://alion.io/company/jabil","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":78,"open_postings":454,"ghost_share":0.004,"stale_share":0.87,"repost_share":0.015,"time_to_fill_p50_days":31,"computed_at":"2026-10-22T06:10:10Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","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":["Singapore"],"countries":["SG"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":33000,"max_usd":61000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":273},"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":"2026-08-11T00:00:00Z","employer_posted_date":"2026-08-11","last_verified_at":"2026-10-22T23:34:23Z","board_verified":true,"closed_at":null,"days_open":73,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":73},"description":"At Jabil (NYSE: JBL), we are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, supply chain, and manufacturing solutions. With 60 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe.Job Title: Supplier Quality Engineer - Medical Devices\nJob Summary\nWe are seeking a detail-oriented Supplier Quality Engineer (SQE) with experience in the medical device, healthcare products, or pharmaceutical industry to ensure the quality, compliance, and performance of suppliers throughout the supply chain. The ideal candidate will be responsible for supplier qualification, supplier audits, quality improvement initiatives, incoming quality management, and ensuring compliance with regulatory and quality requirements including ISO 13485, FDA 21 CFR Part 820, ISO 14971, and GMP.\nKey Responsibilities\nSupplier Quality Management\nLead supplier qualification, approval, and onboarding activities to ensure compliance with company and regulatory requirements.\nConduct supplier risk assessments and establish supplier quality agreements.\nMonitor supplier performance through key quality metrics, including PPM, SCAR closure, on-time delivery, audit performance, and non-conformance trends.\nDevelop and maintain approved supplier lists (ASL).\nSupplier Audits & Compliance\nPlan, perform, and lead supplier audits to assess compliance with ISO 13485, GMP, FDA QSR, and company quality requirements.\nSupport regulatory inspections and external audits involving supplier-related processes.\nTrack audit findings and ensure timely closure of corrective actions.\nSupplier Corrective Actions\nLead Supplier Corrective Action Requests (SCAR) investigations and resolution activities.\nConduct root cause analysis using quality tools such as 5 Whys, Fishbone Diagram, and Fault Tree Analysis.\nVerify effectiveness of implemented corrective and preventive actions.\nIncoming Quality & Non-Conformance Management\nManage supplier-related non-conformances and material quality issues.\nReview and disposition incoming inspection failures and supplier complaints.\nImplement containment actions and coordinate supplier investigations.\nDrive reduction of supplier defects and improve incoming quality performance.\nNew Product Introduction (NPI) Support\nPartner with R&D, Manufacturing, Purchasing, and Regulatory Affairs teams to support supplier selection for new products.\nReview supplier process validation documentation and manufacturing capabilities.\nEnsure supplier readiness for new product launches and engineering changes.\nRisk Management\nParticipate in supplier risk management activities in accordance with ISO 14971.\nSupport PFMEA, DFMEA, process risk assessments, and supplier risk mitigation plans.\nEvaluate critical component suppliers and establish appropriate monitoring controls.\nValidation & Change Control\nReview supplier validation documentation, including IQ/OQ/PQ and process validation reports.\nAssess supplier change notifications and ensure compliance with change control requirements.\nSupport qualification and requalification of supplier manufacturing processes.\nContinuous Improvement\nDrive supplier quality improvement initiatives using Lean Manufacturing and Six Sigma methodologies.\nAnalyze supplier quality trends and develop improvement plans.\nCollaborate with suppliers to reduce defects, improve process capability, and enhance product quality.\nDocumentation & Compliance\nMaintain supplier quality records in accordance with QMS requirements.\nEnsure supplier documentation complies with ISO 13485, FDA requirements, GMP, and internal procedures.\nSupport document control activities related to supplier quality and compliance.\nQMS - Additional responsibility\nSupport and maintain the Quality Management System (QMS) in compliance with ISO 13485 and regulatory requirements.\nLead and support CAPA (Corrective and Preventive Actions) investigations, root cause analysis, and effectiveness checks.\nPerform Internal Audits, Supplier Audits, and support external regulatory audits (FDA, notified bodies).\nReview and approve design documentation, including DHF (Design History File), DMR (Device Master Record), and DHR (Device History Record).\nParticipate in risk management activities (ISO 14971), including hazard analysis, FMEA, and risk control implementation.\nCollaborate with cross-functional teams (R&D, Manufacturing, Regulatory Affairs) for new product development and process validation.\nEnsure compliance with Good Manufacturing Practices (GMP) and quality standards.\nHandle non-conformance reports (NCR) and lead investigations for product or process deviations.\nSupport validation activities (IQ/OQ/PQ, software validation, process validation).\nDrive supplier quality management, including qualification, monitoring, and performance evaluation.\nAnalyze quality data and implement continuous improvement initiatives (Lean, Six Sigma).\nRequired Qualifications\nBachelor's Degree in Engineering, Biomedical Engineering, Manufacturing Engineering, Quality Engineering, Life Sciences, or related discipline.\n3-8 years of experience in Supplier Quality Engineering, Quality Engineering, or Supplier Development within Medical Devices, Healthcare Products, Electronics Manufacturing, or Pharmaceutical industries.\nStrong knowledge of:ISO 13485\nFDA 21 CFR Part 820\nISO 14971\nGMP\nSupplier Quality Management Systems\n\nExperience conducting supplier audits and managing supplier corrective actions.\nStrong root cause investigation and problem-solving skills.\nExperience with incoming quality control, supplier qualification, and supplier performance monitoring.\nKnowledge of quality tools and methodologies:SPC\nCAPA\n8D\n5 Why Analysis\nFishbone Analysis\nFMEA\nSix Sigma\n\nPreferred Qualifications\nASQ Certified Quality Engineer (CQE).\nSix Sigma Green Belt or Black Belt certification.\nExperience with Class II/III Medical Devices.\nExperience with sterile products and regulated manufacturing environments.\nKnowledge of supplier validation and process qualification requirements.\nExperience with electronic QMS systems (eQMS).\nExperience in:Supplier Development\nContract Manufacturing Organizations (CMO)\nSMT (PCBA Manufacturing)\nHigh Level Assembly (HLA) Manufacturing\nMechanical Components and Electromechanical Assemblies\n\nFamiliarity with regulatory submissions such as CE Marking and FDA 510(k).\nKey Competencies\nSupplier Quality Management\nSupplier Development and Relationship Management\nAudit and Compliance Expertise\nRisk Assessment and Mitigation\nStrong Analytical and Problem-Solving Skills\nEffective Communication and Negotiation Skills\nCross-Functional Collaboration\nContinuous Improvement Mindset\nAttention to Detail and Regulatory Compliance Focus\nWork Environment\nOffice and manufacturing floor interaction.\nDomestic and international travel for supplier audits, supplier development activities, and qualification visits.\nParticipation in regulatory inspections and quality system audits.\nExample KPIs\nSupplier PPM (Parts Per Million Defects)\nSupplier Audit Compliance Score\nSCAR Closure Cycle Time\nIncoming Quality Acceptance Rate\nSupplier On-Time Corrective Action Closure\nSupplier Quality Improvement Metrics\nCost of Poor Supplier Quality (COPQ)\nReduction in Supplier-Related Non-Conformances\nSupplier Risk Reduction Effectiveness\nApproved Supplier Performance Rating\nBE AWARE OF FRAUD: When applying for a job at Jabil you will be contacted via correspondence through our official job portal with a jabil.com e-mail address; direct phone call from a member of the Jabil team; or direct e-mail with a jabil.com e-mail address. Jabil does not request payments for interviews or at any other point during the hiring process. Jabil will not ask for your personal identifying information such as a social security number, birth certificate, financial institution, driver’s license number or passport information over the phone or via e-mail. If you believe you are a victim of identity theft, contact your local police department. Any scam job listings should be reported to whatever website it was posted in.Jabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, genetic information, veteran status, or any other characteristic protected by law.\nAccessibility Accommodation\nIf you are a qualified individual with a disability, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access Jabil.com/Careers site as a result of your disability. You can request a reasonable accommodation by sending an e-mail to  with the nature of your request and contact information. Please do not direct any other general employment related questions to this e-mail. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to.#whereyoubelong","description_format":"text","description_chars":9309,"description_truncated":false,"requirements":{"experience_years_min":3,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":false},"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Electronics Manufacturing","Contract Manufacturing"],"lifecycle":[{"event":"open","at":"2026-10-18T18:11:55Z"}],"visa":[],"liveness":{"score":7,"band":"cold","label":"Long shot","p_open":1,"p_active":0.26,"p_room":0.28,"age_days":72,"expected_fill_days":31,"reasons":["conf:1","stale_co","evergreen","velocity","win:tail","crowd:brand"],"computed_at":"2026-10-22T06:10:10Z"},"pay":null,"html_url":"https://alion.io/job/jabil-supplier-quality-engineer-2","json_url":"https://alion.io/job/jabil-supplier-quality-engineer-2.json","meta":{"generated_at":"2026-10-23T01:56:44Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","about":"Alion is a live layer of people, companies and AI agents: who they are, whether they are real and active right now, what they do and how to work with them, readable by people and by agents and paid per call.","catalog":"https://alion.io/catalog.json","usage":{"tier":"crawler_verified","counted_by":"address","units_charged":1,"used_today":3221,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-10-24T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.02,"usd":0.002,"plus_per_slice":{"credits":0.05,"usd":0.005}},"unit":"per company, plus each slice with data","note":"the employer in depth","call":{"mcp_tool":"get_company","arguments":{"id":87},"rest":"https://alion.io/mcp/rest/get_company?id=87"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fjabil-supplier-quality-engineer-2"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"live","price":{"credits":1,"usd":0.1},"unit":"per slice","note":"pay, demand and time to fill for this role and place","call":{"mcp_tool":"market_stats"},"human":"https://alion.io/catalog?offer=market.stats&for=job%2Fjabil-supplier-quality-engineer-2"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.02,"usd":0.002},"unit":"per posting in a list","note":"similar open postings","call":{"mcp_tool":"search_jobs"},"human":"https://alion.io/catalog?offer=job.search&for=job%2Fjabil-supplier-quality-engineer-2"},{"id":"company.verify","title":"Is this company real and active right now","status":"pilot","price":null,"unit":"per company","request":{"url":"https://alion.io/catalog/request","method":"POST","body":"{\"offer\": \"company.verify\", \"for\": \"job/jabil-supplier-quality-engineer-2\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fjabil-supplier-quality-engineer-2"}]}