{"schemaVersion":"jobsearcher.job.v1","id":"3e77fc45d9e48d0180aca864","url":"https://jobsearcher.com/jobs/3e77fc45d9e48d0180aca864","canonicalUrl":"https://jobsearcher.com/jobs/3e77fc45d9e48d0180aca864","title":"Process Engineer - Pharma","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\nJob Responsibilities:\n\nResponsibilities include but are not limited to:\n\nProcess Optimization & Manufacturing Support\n\nProvide day-to-day engineering support to pharmaceutical manufacturing operations.\n\nAnalyze manufacturing processes to identify opportunities for improving efficiency, quality, yield, and cost.\n\nTroubleshoot process issues and implement corrective and preventive actions (CAPAs).\n\nMonitor process performance through data analysis and key performance indicators (KPIs).\n\nLead root cause investigations related to process deviations, nonconformances, and customer complaints.\n\nValidation & Compliance\n\nSupport process validation, equipment qualification, and revalidation activities.\n\nDevelop and execute validation protocols, reports, and technical documentation.\n\nEnsure compliance with FDA regulations, cGMP requirements, BD policies, and applicable quality standards.\n\nSupport internal and external audits, inspections, and regulatory commitments.\n\nMaintain manufacturing documentation, standard operating procedures (SOPs), and work instructions.\n\nContinuous Improvement\n\nLead Lean Manufacturing and Continuous Improvement projects.\n\nUtilize Six Sigma, DMAIC, and problem-solving methodologies to eliminate waste and improve process capability.\n\nIdentify and implement productivity, quality, and cost-reduction initiatives.\n\nParticipate in site transformation and operational excellence programs.\n\nProject Management\n\nSupport new product introductions, technology transfers, and process changes.\n\nCoordinate engineering projects from conception through implementation.\n\nManage timelines, risk assessments, resource requirements, and project documentation.\n\nCollaborate with Maintenance, Quality, Operations, Validation, Regulatory Affairs, and Supply Chain teams.\n\nSafety & Quality\n\nPromote a strong culture of safety, compliance, and quality.\n\nSupport risk assessments, process hazard evaluations, and quality improvement initiatives.\n\nEnsure all engineering activities are performed following EHS and Quality Management System requirements.\n\nEducation and Experience:\n\nBachelor’s degree in Chemical Engineering, Industrial Engineering, Mechanical Engineering, Biomedical\n\n3+ years of experience of engineering experience within a pharmaceutical, medical device, biotechnology, or highly regulated manufacturing environment\n\nExperience working in FDA-regulated, cGMP, validation, and quality systems.\n\nExperience in pharmaceutical manufacturing and aseptic or sterilization processes preferred.\n\nKnowledge of process validation, equipment qualification (IQ/OQ/PQ), and risk management methodologies, preferred.\n\nLean Six Sigma Green Belt or Black Belt certification preferred.\n\nExperience with SAP, TrackWise, MES, or other manufacturing systems preferred.\n\nKnowledge of statistical tools and process capability analysis.\n\nBilingual (English/Spanish) preferred.\n\nKnowledge and Skills:\n\nTechnical Skills\n\nStrong analytical and problem-solving skills.\n\nExperience conducting root cause investigations and implementing CAPAs.\n\nProficiency in Microsoft Office applications and data analysis tools.\n\nKey Competencies\n\nStrong problem-solving and analytical skills\n\nDetail-oriented with data-driven decision making\n\nAbility to manage problem solving and critical thinking\n\nEffective communication and collaboration across all levels\n\nPhysical Demands:\n\nManufacturing environment with exposure to production areas.\n\nWork Environment:\n\nManufacturing\n\nWhy Join Us?\nTo find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.\n\nWe believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.\n\nTo learn more about BD visit https://bd.com/careers.\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\nPrimary Work Location\nUSA TX - El Paso - Northwestern Dr.\n\n#J-18808-Ljbffr","company":"Bdx","rawCompany":"bdx","city":"El Paso","state":"TX","isRemote":false,"isActive":true,"createdAt":"2026-08-19T03:19:02.719Z","occupations":[{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2112.00","title":"Industrial Engineers","slug":"industrial-engineers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"325411","title":"Medicinal and Botanical Manufacturing","slug":"medicinal-and-botanical-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer - Pharma","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\nJob Responsibilities:\n\nResponsibilities include but are not limited to:\n\nProcess Optimization & Manufacturing Support\n\nProvide day-to-day engineering support to pharmaceutical manufacturing operations.\n\nAnalyze manufacturing processes to identify opportunities for improving efficiency, quality, yield, and cost.\n\nTroubleshoot process issues and implement corrective and preventive actions (CAPAs).\n\nMonitor process performance through data analysis and key performance indicators (KPIs).\n\nLead root cause investigations related to process deviations, nonconformances, and customer complaints.\n\nValidation & Compliance\n\nSupport process validation, equipment qualification, and revalidation activities.\n\nDevelop and execute validation protocols, reports, and technical documentation.\n\nEnsure compliance with FDA regulations, cGMP requirements, BD policies, and applicable quality standards.\n\nSupport internal and external audits, inspections, and regulatory commitments.\n\nMaintain manufacturing documentation, standard operating procedures (SOPs), and work instructions.\n\nContinuous Improvement\n\nLead Lean Manufacturing and Continuous Improvement projects.\n\nUtilize Six Sigma, DMAIC, and problem-solving methodologies to eliminate waste and improve process capability.\n\nIdentify and implement productivity, quality, and cost-reduction initiatives.\n\nParticipate in site transformation and operational excellence programs.\n\nProject Management\n\nSupport new product introductions, technology transfers, and process changes.\n\nCoordinate engineering projects from conception through implementation.\n\nManage timelines, risk assessments, resource requirements, and project documentation.\n\nCollaborate with Maintenance, Quality, Operations, Validation, Regulatory Affairs, and Supply Chain teams.\n\nSafety & Quality\n\nPromote a strong culture of safety, compliance, and quality.\n\nSupport risk assessments, process hazard evaluations, and quality improvement initiatives.\n\nEnsure all engineering activities are performed following EHS and Quality Management System requirements.\n\nEducation and Experience:\n\nBachelor’s degree in Chemical Engineering, Industrial Engineering, Mechanical Engineering, Biomedical\n\n3+ years of experience of engineering experience within a pharmaceutical, medical device, biotechnology, or highly regulated manufacturing environment\n\nExperience working in FDA-regulated, cGMP, validation, and quality systems.\n\nExperience in pharmaceutical manufacturing and aseptic or sterilization processes preferred.\n\nKnowledge of process validation, equipment qualification (IQ/OQ/PQ), and risk management methodologies, preferred.\n\nLean Six Sigma Green Belt or Black Belt certification preferred.\n\nExperience with SAP, TrackWise, MES, or other manufacturing systems preferred.\n\nKnowledge of statistical tools and process capability analysis.\n\nBilingual (English/Spanish) preferred.\n\nKnowledge and Skills:\n\nTechnical Skills\n\nStrong analytical and problem-solving skills.\n\nExperience conducting root cause investigations and implementing CAPAs.\n\nProficiency in Microsoft Office applications and data analysis tools.\n\nKey Competencies\n\nStrong problem-solving and analytical skills\n\nDetail-oriented with data-driven decision making\n\nAbility to manage problem solving and critical thinking\n\nEffective communication and collaboration across all levels\n\nPhysical Demands:\n\nManufacturing environment with exposure to production areas.\n\nWork Environment:\n\nManufacturing\n\nWhy Join Us?\nTo find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.\n\nWe believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.\n\nTo learn more about BD visit https://bd.com/careers.\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\nPrimary Work Location\nUSA TX - El Paso - Northwestern Dr.\n\n#J-18808-Ljbffr","datePosted":"2026-08-19T03:19:02.719Z","dateModified":"2026-08-19T03:19:02.719Z","hiringOrganization":{"@type":"Organization","name":"Bdx","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"El Paso","addressRegion":"TX","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"3e77fc45d9e48d0180aca864"},"url":"https://jobsearcher.com/jobs/3e77fc45d9e48d0180aca864"}}