{"schemaVersion":"jobsearcher.job.v1","id":"db2ed3d1e0b3fea09b0d8301","url":"https://jobsearcher.com/jobs/db2ed3d1e0b3fea09b0d8301","canonicalUrl":"https://jobsearcher.com/jobs/db2ed3d1e0b3fea09b0d8301","title":"Engineer ProQN844","description":"Title: Engineer ProQN844\n\nLocation: East of Puerto Rico\n\nEligibility: Puerto Rico Residents Only\n\nPosition: 1 Opening\n\nWork Arrangement: Onsite\n\nContract: 1 Year\n\nSchedule: Administrative Shift, with availability to support non-standard shifts based on business needs\n\nPosition Summary\n\nOur client is seeking an Engineer to support process optimization, troubleshooting, manufacturing operations, and engineering projects within a highly regulated pharmaceutical/biotechnology environment.\n\nThe ideal candidate will have an engineering background, strong analytical and problem-solving skills, and the ability to apply engineering principles to operational challenges, system modifications, validation activities, and projects of limited to moderate scope and complexity.\n\nKey Responsibilities\n\nSupport process optimization and troubleshooting activities within operations, manufacturing, pilot plant, or capital project environments.\nApply engineering principles to support system modifications, experiments, and capital projects.\nAnalyze operational and engineering data and present clear interpretations and recommendations.\nProvide solutions to technical problems of moderate scope and complexity.\nEvaluate and apply standard engineering techniques and procedures under general supervision.\nComplete routine technical assignments and investigations involving a limited number of variables.\nServe as a technical resource for equipment and systems troubleshooting.\nSupport daily operations when needed to meet schedules or resolve complex technical issues.\nAssess the operational performance and regulatory compliance of equipment and systems.\nCollaborate with Research, Manufacturing, Maintenance, Process Development, Utilities, Facilities, Quality Assurance, and Validation teams.\nSupport the development of requirements and recommendations for system modifications.\nAssist project managers with design, engineering, and construction projects while maintaining schedule and budget requirements.\nCollaborate with consultants, architects, and engineering firms on standard design documentation.\nReview and evaluate quotes for equipment modifications or installations.\nPrepare basic project cost estimates and schedules.\nPerform additional functions as assigned based on business needs.\n\nPreferred Qualifications\n\nChemical Engineering background preferred.\nExperience with Statistical Analysis.\nBiotechnology industry experience is a plus.\nExperience with Drug Substance Manufacturing or technical support is a plus.\nWorking knowledge of pharmaceutical/biotechnology processes.\nFamiliarity with validation processes and validation protocol execution.\nFamiliarity with documentation requirements in a highly regulated environment.\nAbility to interpret and apply GLP and GMP requirements.\nAbility to apply engineering principles to manufacturing operations.\nExperience developing solutions to routine technical problems.\nAbility to operate specialized laboratory equipment and computer systems as required.\nStrong problem-solving and applied engineering skills.\nBasic technical report writing and presentation skills.\nStrong verbal communication skills.\nStrong personal organization and ability to manage change.\nFamiliarity with validation protocol writing.\nStrong analytical problem-solving skills and computer literacy.\nTechnical knowledge related to equipment and systems.\n\nEducation & Experience\n\nMaster’s degree, OR\nBachelor’s degree in Engineering with 2 years of engineering experience.\n\nInterested candidates: Please submit your updated resume through ProQuality Network or contact our recruiting team for consideration.","company":"Proqualitynetwork","rawCompany":"proqualitynetwork","city":"Juncos","state":"PR","isRemote":false,"isActive":false,"createdAt":"2026-10-16T11:33:09.335Z","occupations":[{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Engineer ProQN844","description":"Title: Engineer ProQN844\n\nLocation: East of Puerto Rico\n\nEligibility: Puerto Rico Residents Only\n\nPosition: 1 Opening\n\nWork Arrangement: Onsite\n\nContract: 1 Year\n\nSchedule: Administrative Shift, with availability to support non-standard shifts based on business needs\n\nPosition Summary\n\nOur client is seeking an Engineer to support process optimization, troubleshooting, manufacturing operations, and engineering projects within a highly regulated pharmaceutical/biotechnology environment.\n\nThe ideal candidate will have an engineering background, strong analytical and problem-solving skills, and the ability to apply engineering principles to operational challenges, system modifications, validation activities, and projects of limited to moderate scope and complexity.\n\nKey Responsibilities\n\nSupport process optimization and troubleshooting activities within operations, manufacturing, pilot plant, or capital project environments.\nApply engineering principles to support system modifications, experiments, and capital projects.\nAnalyze operational and engineering data and present clear interpretations and recommendations.\nProvide solutions to technical problems of moderate scope and complexity.\nEvaluate and apply standard engineering techniques and procedures under general supervision.\nComplete routine technical assignments and investigations involving a limited number of variables.\nServe as a technical resource for equipment and systems troubleshooting.\nSupport daily operations when needed to meet schedules or resolve complex technical issues.\nAssess the operational performance and regulatory compliance of equipment and systems.\nCollaborate with Research, Manufacturing, Maintenance, Process Development, Utilities, Facilities, Quality Assurance, and Validation teams.\nSupport the development of requirements and recommendations for system modifications.\nAssist project managers with design, engineering, and construction projects while maintaining schedule and budget requirements.\nCollaborate with consultants, architects, and engineering firms on standard design documentation.\nReview and evaluate quotes for equipment modifications or installations.\nPrepare basic project cost estimates and schedules.\nPerform additional functions as assigned based on business needs.\n\nPreferred Qualifications\n\nChemical Engineering background preferred.\nExperience with Statistical Analysis.\nBiotechnology industry experience is a plus.\nExperience with Drug Substance Manufacturing or technical support is a plus.\nWorking knowledge of pharmaceutical/biotechnology processes.\nFamiliarity with validation processes and validation protocol execution.\nFamiliarity with documentation requirements in a highly regulated environment.\nAbility to interpret and apply GLP and GMP requirements.\nAbility to apply engineering principles to manufacturing operations.\nExperience developing solutions to routine technical problems.\nAbility to operate specialized laboratory equipment and computer systems as required.\nStrong problem-solving and applied engineering skills.\nBasic technical report writing and presentation skills.\nStrong verbal communication skills.\nStrong personal organization and ability to manage change.\nFamiliarity with validation protocol writing.\nStrong analytical problem-solving skills and computer literacy.\nTechnical knowledge related to equipment and systems.\n\nEducation & Experience\n\nMaster’s degree, OR\nBachelor’s degree in Engineering with 2 years of engineering experience.\n\nInterested candidates: Please submit your updated resume through ProQuality Network or contact our recruiting team for consideration.","datePosted":"2026-10-16T11:33:09.335Z","dateModified":"2026-10-16T11:33:09.335Z","hiringOrganization":{"@type":"Organization","name":"Proqualitynetwork","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Juncos","addressRegion":"PR","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"db2ed3d1e0b3fea09b0d8301"},"url":"https://jobsearcher.com/jobs/db2ed3d1e0b3fea09b0d8301"}}