{"schemaVersion":"jobsearcher.job.v1","id":"c1657d53a511ea170399c24b","url":"https://jobsearcher.com/jobs/c1657d53a511ea170399c24b","canonicalUrl":"https://jobsearcher.com/jobs/c1657d53a511ea170399c24b","title":"Sr. Quality Engineer","description":"We are the people who give possibilities purpose\n\nBD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.\n\nJob Description\nJoin our team as a Senior Design Quality Engineer where you’ll be the guardian of quality for our critical product family, directly protecting patient safety and business risk while driving innovation in medical device development!\n\nYou’ll work at the intersection of innovation and compliance, ensuring every change we make is robust, validated, and protects both our patients and our business.\n\nResponsibilities\n\nQuality Leadership Across the Product Lifecycle: Serve as the Quality Assurance expert for your entire product line, owning Design Control, Document Control, and QA processes from concept to commercialization\n\nStrategic Partnership: Collaborate with contract manufacturers and internal plants to seamlessly implement changes while maintaining the highest quality standards\n\nProactive Risk Management: Monitor complaint trends like a detective, identifying performance drift before it becomes a problem and executing swift corrective actions\n\nSubject Matter Authority: Be the go-to resource for cross‑functional teams in Engineering, Operations, and supplier management\n\n** hamper Design Control Excellence:**Serve as the Quality Representative on Project Teams, ensuring Design Control principles are woven into every Product and Process Change and New Product Development initiative\n\nLead Quality Initiatives: Provide QA leadership for Project Teams and the Quality Department.\n\nMaster Documentation: Build, review, and approve critical Quality System Documents including CAPAs and Audit reports\n\nCraft Compliance Artifacts: Create and approve Design History Files, ensuring every product decision is documented and defensible\n\nValidate Everything: Develop, review, and approve Protocols for Process and Product Validations, Stability studies, and Software Validation documents\n\nAssess and Mitigate Risk: Create comprehensive Risk Assessments using FMEA, FMECA, and FTA methodologies\n\nDevelop Talent: Mentor staff and provide supervision to technicians and engineers, building the next generation of quality professionals\n\nDrive Continuous Improvement: Analyze process and product non‑conformances and implement comprehensive corrective and preventive action plans that stick\n\nAudit with Authority: Conduct Internal and Supplier Quality System Audits to ensure compliance across the supply chain\n\nStay Ahead of the Curve: Maintain active membership in trade and professional organizations, bringing state‑of‑the‑art industry standards back to the team\n\nInvestigate and Resolve: Perform thorough Complaint reviews and investigations, getting to the root cause quickly\n\nTrack Success Metrics: Monitor and trend Quality Indicators to demonstrate continuous improvement\n\nCollaborate Across Sites: Work seamlessly with manufacturing facilities and other Division Facilities to ensure quality consistency\n\nChair Critical Reviews: Serve as Independent QA Reviewer and Chairperson for Design Reviews, making the tough calls when needed\n\nYou’ll be working on critical products that directly impact patient lives. Every validation you approve, every risk assessment you complete, and every trend you identify make a difference.\n\nThis position requires someone who can balance technical expertise with leadership presence, someone who can mentor others while rolling up their sleeves to solve complex quality challenges, and someone who thrives in the dynamic environment where innovation meets regulatory compliance.\n\nRequired Qualifications\n\nBachelor’s Degree in Engineering and 4 Quality Engineering experience in a regulated environment OR\n\nMaster’s Degree and 2 years of Quality Engineering experience in a regulated environment\n\nKnowledge and Skills\n\nGood questioning and problem‑solving skills\n\nDetail oriented and ability to organize large amounts of work and data. This includes the need for good documentation practices.\n\nPlans effectively and team oriented.\n\nRegulatory knowledge and experience including but not limited to FDA, MDSAP, PMDA, CFDA\n\nDemonstrated experience working with international suppliers/manufacturers as it relates to product quality and reliability\n\nDemonstrated history of successfully interpreting regulations, and procedures\n\nDemonstrated skill in statistical analysis and applied statistical methodologies\n\nKnowledge and understanding of IEC 60601 standards\n\nPreferred Requirements\n\nCapital system experience (Electro‑mechanical)\n\nASQ Certification\n\nPrimary Work Location\nUSA GA - Covington BMD\n\nBecton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.\n\n#J-18808-Ljbffr","company":"BD","rawCompany":"bd","city":"Covington","state":"VA","isRemote":false,"isActive":false,"createdAt":"2026-07-19T03:22:52.088Z","occupations":[{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"}],"industries":[{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Sr. Quality Engineer","description":"We are the people who give possibilities purpose\n\nBD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.\n\nJob Description\nJoin our team as a Senior Design Quality Engineer where you’ll be the guardian of quality for our critical product family, directly protecting patient safety and business risk while driving innovation in medical device development!\n\nYou’ll work at the intersection of innovation and compliance, ensuring every change we make is robust, validated, and protects both our patients and our business.\n\nResponsibilities\n\nQuality Leadership Across the Product Lifecycle: Serve as the Quality Assurance expert for your entire product line, owning Design Control, Document Control, and QA processes from concept to commercialization\n\nStrategic Partnership: Collaborate with contract manufacturers and internal plants to seamlessly implement changes while maintaining the highest quality standards\n\nProactive Risk Management: Monitor complaint trends like a detective, identifying performance drift before it becomes a problem and executing swift corrective actions\n\nSubject Matter Authority: Be the go-to resource for cross‑functional teams in Engineering, Operations, and supplier management\n\n** hamper Design Control Excellence:**Serve as the Quality Representative on Project Teams, ensuring Design Control principles are woven into every Product and Process Change and New Product Development initiative\n\nLead Quality Initiatives: Provide QA leadership for Project Teams and the Quality Department.\n\nMaster Documentation: Build, review, and approve critical Quality System Documents including CAPAs and Audit reports\n\nCraft Compliance Artifacts: Create and approve Design History Files, ensuring every product decision is documented and defensible\n\nValidate Everything: Develop, review, and approve Protocols for Process and Product Validations, Stability studies, and Software Validation documents\n\nAssess and Mitigate Risk: Create comprehensive Risk Assessments using FMEA, FMECA, and FTA methodologies\n\nDevelop Talent: Mentor staff and provide supervision to technicians and engineers, building the next generation of quality professionals\n\nDrive Continuous Improvement: Analyze process and product non‑conformances and implement comprehensive corrective and preventive action plans that stick\n\nAudit with Authority: Conduct Internal and Supplier Quality System Audits to ensure compliance across the supply chain\n\nStay Ahead of the Curve: Maintain active membership in trade and professional organizations, bringing state‑of‑the‑art industry standards back to the team\n\nInvestigate and Resolve: Perform thorough Complaint reviews and investigations, getting to the root cause quickly\n\nTrack Success Metrics: Monitor and trend Quality Indicators to demonstrate continuous improvement\n\nCollaborate Across Sites: Work seamlessly with manufacturing facilities and other Division Facilities to ensure quality consistency\n\nChair Critical Reviews: Serve as Independent QA Reviewer and Chairperson for Design Reviews, making the tough calls when needed\n\nYou’ll be working on critical products that directly impact patient lives. Every validation you approve, every risk assessment you complete, and every trend you identify make a difference.\n\nThis position requires someone who can balance technical expertise with leadership presence, someone who can mentor others while rolling up their sleeves to solve complex quality challenges, and someone who thrives in the dynamic environment where innovation meets regulatory compliance.\n\nRequired Qualifications\n\nBachelor’s Degree in Engineering and 4 Quality Engineering experience in a regulated environment OR\n\nMaster’s Degree and 2 years of Quality Engineering experience in a regulated environment\n\nKnowledge and Skills\n\nGood questioning and problem‑solving skills\n\nDetail oriented and ability to organize large amounts of work and data. This includes the need for good documentation practices.\n\nPlans effectively and team oriented.\n\nRegulatory knowledge and experience including but not limited to FDA, MDSAP, PMDA, CFDA\n\nDemonstrated experience working with international suppliers/manufacturers as it relates to product quality and reliability\n\nDemonstrated history of successfully interpreting regulations, and procedures\n\nDemonstrated skill in statistical analysis and applied statistical methodologies\n\nKnowledge and understanding of IEC 60601 standards\n\nPreferred Requirements\n\nCapital system experience (Electro‑mechanical)\n\nASQ Certification\n\nPrimary Work Location\nUSA GA - Covington BMD\n\nBecton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.\n\n#J-18808-Ljbffr","datePosted":"2026-07-19T03:22:52.088Z","dateModified":"2026-07-19T03:22:52.088Z","hiringOrganization":{"@type":"Organization","name":"BD","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Covington","addressRegion":"VA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"c1657d53a511ea170399c24b"},"url":"https://jobsearcher.com/jobs/c1657d53a511ea170399c24b"}}