{"schemaVersion":"jobsearcher.job.v1","id":"4d5b65cd576b46174dd3f75f","url":"https://jobsearcher.com/jobs/4d5b65cd576b46174dd3f75f","canonicalUrl":"https://jobsearcher.com/jobs/4d5b65cd576b46174dd3f75f","title":"Manufacturing Engineer","description":"EQVAL Group, Inc. is a company that provides services to the manufacturing industry (Medical Devices, Pharmaceuticals, Biotechnologies, others). We work with an extraordinary group of professionals (employees and contractors) to accomplish the requirements established by our customers, in order to perform and provide a highly effective service.\nThe Manufacturing Engineer will support New Products Introduction (NPI) and Process transfer activities in a regulated manufacturing environment.\nResponsible to generate and execute validation protocols for new or replaced equipment, or process changes. Perform initial set-up, conduct and/or support troubleshooting, including continuous improvement, of production equipment and processes. Support investigations process (NCRs, Complaints) and teams with Manufacturing and QA personnel for review and disposition of investigations on time.\nMinimum Requirements:\nBachelor Degree in an Engineering Field.\n3+ years of knowledge and experience in cGMP in a Medical Devices manufacturing environment.\n3+ years of equipment qualification and process validation knowledge (IQ, OQ, PQ protocols generation and execution, deviations and reports generation).\n3+ years of statistical analysis (GR&R) and data management (including the usage of statistical tools, i.e, Minitab).\nKnowledge and skills (1-3 years) in diverse areas such as: Investigations (NCRs, Complaints, CAPA), Lean Manufacturing and Six Sigma Tools.\nKnowledge with pFMEA (analysis and development).\nHighly Motivated, Self Starter and Multi Task Oriented.\nComputer literate (Word, Excel, Power Point, Minitab).\nExcellent communicator (spoken, written) in both, English and Spanish.\nOnly local candidates will be considered.\nJob Types: Full-time, Contract\nBenefits:\nDental insurance\nEmployee assistance program\nEmployee discount\nHealth insurance\nLife insurance\nPaid time off\nProfessional development assistance\nReferral program\nSchedule:\n8 hour shift\nMonday to Friday\nWeekends as needed\nAbility to Relocate:\nVillalba, PR: Relocate before starting work (Required)\nWork Location: In person","company":"Engineeringqualityandvalidation","rawCompany":"engineeringqualityandvalidation","city":"Juarez","state":"Chih","isRemote":false,"isActive":false,"createdAt":"2026-04-12T20:32:17.907Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.00","title":"Industrial Engineers","slug":"industrial-engineers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Manufacturing Engineer","description":"EQVAL Group, Inc. is a company that provides services to the manufacturing industry (Medical Devices, Pharmaceuticals, Biotechnologies, others). We work with an extraordinary group of professionals (employees and contractors) to accomplish the requirements established by our customers, in order to perform and provide a highly effective service.\nThe Manufacturing Engineer will support New Products Introduction (NPI) and Process transfer activities in a regulated manufacturing environment.\nResponsible to generate and execute validation protocols for new or replaced equipment, or process changes. Perform initial set-up, conduct and/or support troubleshooting, including continuous improvement, of production equipment and processes. Support investigations process (NCRs, Complaints) and teams with Manufacturing and QA personnel for review and disposition of investigations on time.\nMinimum Requirements:\nBachelor Degree in an Engineering Field.\n3+ years of knowledge and experience in cGMP in a Medical Devices manufacturing environment.\n3+ years of equipment qualification and process validation knowledge (IQ, OQ, PQ protocols generation and execution, deviations and reports generation).\n3+ years of statistical analysis (GR&R) and data management (including the usage of statistical tools, i.e, Minitab).\nKnowledge and skills (1-3 years) in diverse areas such as: Investigations (NCRs, Complaints, CAPA), Lean Manufacturing and Six Sigma Tools.\nKnowledge with pFMEA (analysis and development).\nHighly Motivated, Self Starter and Multi Task Oriented.\nComputer literate (Word, Excel, Power Point, Minitab).\nExcellent communicator (spoken, written) in both, English and Spanish.\nOnly local candidates will be considered.\nJob Types: Full-time, Contract\nBenefits:\nDental insurance\nEmployee assistance program\nEmployee discount\nHealth insurance\nLife insurance\nPaid time off\nProfessional development assistance\nReferral program\nSchedule:\n8 hour shift\nMonday to Friday\nWeekends as needed\nAbility to Relocate:\nVillalba, PR: Relocate before starting work (Required)\nWork Location: In person","datePosted":"2026-04-12T20:32:17.907Z","dateModified":"2026-04-12T20:32:17.907Z","hiringOrganization":{"@type":"Organization","name":"Engineeringqualityandvalidation","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Juarez","addressRegion":"Chih","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"4d5b65cd576b46174dd3f75f"},"url":"https://jobsearcher.com/jobs/4d5b65cd576b46174dd3f75f"}}