{"schemaVersion":"jobsearcher.job.v1","id":"aa274437b3214d6fec5ee9c2","url":"https://jobsearcher.com/jobs/aa274437b3214d6fec5ee9c2","canonicalUrl":"https://jobsearcher.com/jobs/aa274437b3214d6fec5ee9c2","title":"Process Engineer I","description":"Recommends and implements equipment and process modifications to meet quality standards and improve production efficiencies, manufacturing techniques as well as production yields for existing or new products. Integrates equipment and material capabilities to meet process module target specifications and technology target specifications. Reviews product development requirements for compatibility with processing methods to determine costs and schedules. Interacts with product design and development personnel to ensure that processes and designs are compatible. May develop and conduct statistical analysis or recommend additions to document work. Leads the innovation, development and/or optimization of new manufacturing concepts, processes and procedures for transfer to manufacturing operations.\nWork in new products and capacity increase projects. Main tasks will be to work with all documents of the validation lifecycle including development, execution and closure of documents/reports. Needs to be able to work with root cause analysis and troubleshoot process, product and equipment as needed.\nDuties/Responsibilities:\nTroubleshooting skills\nValidation lifecycle\nInvestigation/Root cause analysis\nTechnical Writing\nFully bilingual\n1st Shift (Administrative Shift)\nEducation/Experience:\nBachelor of Science in Engineering with 2 or more years of relevant experience\nJob Types: Full-time, Contract\nBenefits:\nPaid time off\nSchedule:\n8 hour shift\nDay shift\nMonday to Friday\nEducation:\nBachelor's (Required)\nExperience:\nValidation Lifecycle: 2 years (Preferred)\nRoot cause analysis: 2 years (Preferred)\nTechnical writing: 2 years (Preferred)\nLanguage:\nBilingual (English/Spanish) (Preferred)\nWork Location: In person","company":"Professional Pharma Solutions","rawCompany":"professional pharma solutions","city":"Ponce","state":"PR","isRemote":false,"isActive":false,"createdAt":"2026-04-12T21:16:25.377Z","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":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"333248","title":"All Other Industrial Machinery Manufacturing","slug":"all-other-industrial-machinery-manufacturing"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer I","description":"Recommends and implements equipment and process modifications to meet quality standards and improve production efficiencies, manufacturing techniques as well as production yields for existing or new products. Integrates equipment and material capabilities to meet process module target specifications and technology target specifications. Reviews product development requirements for compatibility with processing methods to determine costs and schedules. Interacts with product design and development personnel to ensure that processes and designs are compatible. May develop and conduct statistical analysis or recommend additions to document work. Leads the innovation, development and/or optimization of new manufacturing concepts, processes and procedures for transfer to manufacturing operations.\nWork in new products and capacity increase projects. Main tasks will be to work with all documents of the validation lifecycle including development, execution and closure of documents/reports. Needs to be able to work with root cause analysis and troubleshoot process, product and equipment as needed.\nDuties/Responsibilities:\nTroubleshooting skills\nValidation lifecycle\nInvestigation/Root cause analysis\nTechnical Writing\nFully bilingual\n1st Shift (Administrative Shift)\nEducation/Experience:\nBachelor of Science in Engineering with 2 or more years of relevant experience\nJob Types: Full-time, Contract\nBenefits:\nPaid time off\nSchedule:\n8 hour shift\nDay shift\nMonday to Friday\nEducation:\nBachelor's (Required)\nExperience:\nValidation Lifecycle: 2 years (Preferred)\nRoot cause analysis: 2 years (Preferred)\nTechnical writing: 2 years (Preferred)\nLanguage:\nBilingual (English/Spanish) (Preferred)\nWork Location: In person","datePosted":"2026-04-12T21:16:25.377Z","dateModified":"2026-04-12T21:16:25.377Z","hiringOrganization":{"@type":"Organization","name":"Professional Pharma Solutions","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Ponce","addressRegion":"PR","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"aa274437b3214d6fec5ee9c2"},"url":"https://jobsearcher.com/jobs/aa274437b3214d6fec5ee9c2"}}