{"schemaVersion":"jobsearcher.job.v1","id":"1b9040ae7fd19e356a6b9c12","url":"https://jobsearcher.com/jobs/1b9040ae7fd19e356a6b9c12","canonicalUrl":"https://jobsearcher.com/jobs/1b9040ae7fd19e356a6b9c12","title":"Process Developement Scientist- ProQN534","description":"Tittle: Senior Process Development Scientist ProQn534\n\nLocation: Juncos, Puerto Rico\n\nWork Schedule: On-site | Administrative Shift (Hybrid)\n\nShift Requirements: Availability to work different shifts and/or weekends based on business needs\n\nPositions Available: 2\n\nContract Duration: 6 months\n\nImportant Notice: This opportunity is available exclusively to direct individual candidates. Third-party contractor submissions, staffing vendors, and Corp-to-Corp (C2C) arrangements will not be considered for this position.\n\nPosition Overview\n\nOur Client is seeking experienced Senior Process Development Scientists to independently conceive, design, implement, and advance scientific experiments that contribute to the successful completion of projects and technical objectives.\n\nThe selected professionals will serve as senior scientific and technical resources, providing advanced data analysis, scientific interpretation, experimental design, and project leadership. This role requires the ability to work independently, develop innovative solutions, collaborate across functions, and support process development and manufacturing initiatives in a regulated pharmaceutical or biotechnology environment.\n\nKey Responsibilities\n\nIndependently plan, monitor, and conduct experiments, studies, or series of experiments to advance projects, technologies, and processes.\nProvide advanced data analysis and interpretation, assess the impact of experimental results, and make scientifically sound recommendations.\nDevelop new and novel experimental designs, protocols, methodologies, and approaches.\nApply scientific theory and critical thinking to solve complex technical and process-related challenges.\nExpand knowledge beyond the core area of expertise and identify relevant external scientific and competitive knowledge.\nServe as a key contributor to research and project teams while providing technical and scientific leadership.\nEstablish productive collaborations across departments and, when appropriate, with external partners.\nIntroduce and evaluate new technologies, methodologies, and scientific concepts.\nDevelop detailed project plans, including timelines, milestones, methodologies, expected results, and required resources.\nMake proactive scientific and technical decisions that support project milestones and business objectives.\nPrepare complex technical documents, reports, protocols, and other scientific documentation.\nMay contribute to scientific publications and technical documents as a lead author.\nSupport department-wide initiatives, including safety programs, recruiting activities, and committees.\nDevelop supervisory, mentoring, and leadership capabilities.\nSupport multiple projects in a fast-paced, regulated manufacturing environment.\n\nEducation & Experience\n\nCandidates must meet one of the following educational and experience combinations:\n\nDoctorate (PhD, PharmD, or MD) with relevant postdoctoral experience, where applicable; or\nMaster’s degree with 3+ years of relevant scientific experience; or\nBachelor’s degree with 5+ years of relevant scientific experience.\n\nA degree in one of the following disciplines is highly preferred:\n\nMechanical Engineering\nChemical Engineering\nBiomedical Engineering\nBioprocess Engineering\nPharmaceutical Sciences\nBiotechnology\nBiology\nMicrobiology\nRelated scientific discipline\n\nRequired Technical Experience\n\nExperience supporting sterile drug product manufacturing within the pharmaceutical or biotechnology industry.\nHands-on experience with aseptic filling operations, process characterization, process validation (PPQ), technology transfer, and commercial process support.\nExperience authoring and executing validation protocols, characterization studies, technical reports, investigations, and change controls.\nStrong knowledge of GMP requirements, aseptic processing principles, contamination control strategies, and pharmaceutical quality systems.\nExperience performing statistical analysis using JMP or Minitab and applying data-driven approaches to process optimization.\nAbility to analyze manufacturing data, identify process trends, and recommend scientifically sound solutions.\nExperience working in cross-functional teams with Manufacturing, Quality, Engineering, Regulatory, and Technical Services.\nStrong technical writing, communication, presentation, and project management skills.\nAbility to independently manage multiple projects while supporting commercial readiness and continuous process improvement.\nExperience with single-use technologies, filling equipment, and sterile manufacturing operations is highly desirable.\nExperience with technical data analysis and scientific documentation.\nProficiency with Microsoft Office, including Excel, Word, and PowerPoint.\nExperience with sample management systems such as LIMS and HLEE.\n\nCore Competencies\n\nThe ideal candidate should demonstrate:\n\nAbility to motivate, lead, and/or supervise the activities of others.\nStrong project management and organizational skills, including the ability to develop realistic timelines.\nStrong problem-solving skills and the ability to apply scientific theory to complex challenges.\nAbility to independently determine and develop scientific analyses and solutions.\nAbility to exercise considerable latitude when establishing scientific work objectives.\nStrong laboratory and project management skills.\nCreativity in developing new hypotheses and approaches for scientific experimentation.\nStrong critical evaluation and detailed interpretation of experimental results.\nUnderstanding of the scientific relevance and business impact of targeted work.\nStrong communication and presentation skills.\nAbility to work effectively in a cross-functional, fast-paced environment.\nBilingual proficiency in English and Spanish.\n\nIdeal Candidate Profile\n\nThe successful candidate will be an experienced scientific professional who can operate independently while providing technical leadership across process development and manufacturing initiatives. The role is particularly suited for someone with hands-on experience in sterile pharmaceutical manufacturing, aseptic processing, filling operations, process validation, data analysis, and technical documentation, combined with strong project management and cross-functional collaboration skills.","company":"Proqualitynetwork","rawCompany":"proqualitynetwork","city":"Juncos","state":"PR","isRemote":false,"isActive":false,"createdAt":"2026-09-14T09:56:33.511Z","occupations":[{"code":"19-1042.00","title":"Medical Scientists, Except Epidemiologists","slug":"medical-scientists-except-epidemiologists"},{"code":"11-9121.00","title":"Natural Sciences Managers","slug":"natural-sciences-managers"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"}],"industries":[{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Developement Scientist- ProQN534","description":"Tittle: Senior Process Development Scientist ProQn534\n\nLocation: Juncos, Puerto Rico\n\nWork Schedule: On-site | Administrative Shift (Hybrid)\n\nShift Requirements: Availability to work different shifts and/or weekends based on business needs\n\nPositions Available: 2\n\nContract Duration: 6 months\n\nImportant Notice: This opportunity is available exclusively to direct individual candidates. Third-party contractor submissions, staffing vendors, and Corp-to-Corp (C2C) arrangements will not be considered for this position.\n\nPosition Overview\n\nOur Client is seeking experienced Senior Process Development Scientists to independently conceive, design, implement, and advance scientific experiments that contribute to the successful completion of projects and technical objectives.\n\nThe selected professionals will serve as senior scientific and technical resources, providing advanced data analysis, scientific interpretation, experimental design, and project leadership. This role requires the ability to work independently, develop innovative solutions, collaborate across functions, and support process development and manufacturing initiatives in a regulated pharmaceutical or biotechnology environment.\n\nKey Responsibilities\n\nIndependently plan, monitor, and conduct experiments, studies, or series of experiments to advance projects, technologies, and processes.\nProvide advanced data analysis and interpretation, assess the impact of experimental results, and make scientifically sound recommendations.\nDevelop new and novel experimental designs, protocols, methodologies, and approaches.\nApply scientific theory and critical thinking to solve complex technical and process-related challenges.\nExpand knowledge beyond the core area of expertise and identify relevant external scientific and competitive knowledge.\nServe as a key contributor to research and project teams while providing technical and scientific leadership.\nEstablish productive collaborations across departments and, when appropriate, with external partners.\nIntroduce and evaluate new technologies, methodologies, and scientific concepts.\nDevelop detailed project plans, including timelines, milestones, methodologies, expected results, and required resources.\nMake proactive scientific and technical decisions that support project milestones and business objectives.\nPrepare complex technical documents, reports, protocols, and other scientific documentation.\nMay contribute to scientific publications and technical documents as a lead author.\nSupport department-wide initiatives, including safety programs, recruiting activities, and committees.\nDevelop supervisory, mentoring, and leadership capabilities.\nSupport multiple projects in a fast-paced, regulated manufacturing environment.\n\nEducation & Experience\n\nCandidates must meet one of the following educational and experience combinations:\n\nDoctorate (PhD, PharmD, or MD) with relevant postdoctoral experience, where applicable; or\nMaster’s degree with 3+ years of relevant scientific experience; or\nBachelor’s degree with 5+ years of relevant scientific experience.\n\nA degree in one of the following disciplines is highly preferred:\n\nMechanical Engineering\nChemical Engineering\nBiomedical Engineering\nBioprocess Engineering\nPharmaceutical Sciences\nBiotechnology\nBiology\nMicrobiology\nRelated scientific discipline\n\nRequired Technical Experience\n\nExperience supporting sterile drug product manufacturing within the pharmaceutical or biotechnology industry.\nHands-on experience with aseptic filling operations, process characterization, process validation (PPQ), technology transfer, and commercial process support.\nExperience authoring and executing validation protocols, characterization studies, technical reports, investigations, and change controls.\nStrong knowledge of GMP requirements, aseptic processing principles, contamination control strategies, and pharmaceutical quality systems.\nExperience performing statistical analysis using JMP or Minitab and applying data-driven approaches to process optimization.\nAbility to analyze manufacturing data, identify process trends, and recommend scientifically sound solutions.\nExperience working in cross-functional teams with Manufacturing, Quality, Engineering, Regulatory, and Technical Services.\nStrong technical writing, communication, presentation, and project management skills.\nAbility to independently manage multiple projects while supporting commercial readiness and continuous process improvement.\nExperience with single-use technologies, filling equipment, and sterile manufacturing operations is highly desirable.\nExperience with technical data analysis and scientific documentation.\nProficiency with Microsoft Office, including Excel, Word, and PowerPoint.\nExperience with sample management systems such as LIMS and HLEE.\n\nCore Competencies\n\nThe ideal candidate should demonstrate:\n\nAbility to motivate, lead, and/or supervise the activities of others.\nStrong project management and organizational skills, including the ability to develop realistic timelines.\nStrong problem-solving skills and the ability to apply scientific theory to complex challenges.\nAbility to independently determine and develop scientific analyses and solutions.\nAbility to exercise considerable latitude when establishing scientific work objectives.\nStrong laboratory and project management skills.\nCreativity in developing new hypotheses and approaches for scientific experimentation.\nStrong critical evaluation and detailed interpretation of experimental results.\nUnderstanding of the scientific relevance and business impact of targeted work.\nStrong communication and presentation skills.\nAbility to work effectively in a cross-functional, fast-paced environment.\nBilingual proficiency in English and Spanish.\n\nIdeal Candidate Profile\n\nThe successful candidate will be an experienced scientific professional who can operate independently while providing technical leadership across process development and manufacturing initiatives. The role is particularly suited for someone with hands-on experience in sterile pharmaceutical manufacturing, aseptic processing, filling operations, process validation, data analysis, and technical documentation, combined with strong project management and cross-functional collaboration skills.","datePosted":"2026-09-14T09:56:33.511Z","dateModified":"2026-09-14T09:56:33.511Z","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":"1b9040ae7fd19e356a6b9c12"},"url":"https://jobsearcher.com/jobs/1b9040ae7fd19e356a6b9c12"}}