{"schemaVersion":"jobsearcher.job.v1","id":"bfee456582dd528de82fba02","url":"https://jobsearcher.com/jobs/bfee456582dd528de82fba02","canonicalUrl":"https://jobsearcher.com/jobs/bfee456582dd528de82fba02","title":"Construction Manager","description":"About GenScript\nGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.\nGenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.\nJob Title: Construction Project Manager\nLocation: Piscataway, NJ (Fully onsite)\nReports to: Director of US Site Operations\nCompensation: The estimated salary range is $120,000 - $150,000, based on experience.\nOverview:\nGenScript is seeking a talented, detail oriented and self-driven individual to join the Operations Department, contributing to the planning, design, construction, commissioning, validation, and engineering process systems development for our facilities in Piscataway, NJ. This position is valid for at least 1-2 years with the opportunity to transition to facility manager after the construction projects are done.\nJob Responsibilities:\nProject Planning and Execution:\nDevelop comprehensive project plans ensuring projects proceed according to set objectives, including requirement gathering, feasibility analysis, risk assessment, and solution formulation.\nManage cost estimation for all project phases and create cost control plans.\nProcurement and Contract Management.\nOversee bidding and procurement for project design, construction, and long-lead equipment.\nManage contract signing and execution with suppliers and contractors, ensuring compliance with terms, quality, and deadlines.\nCompliance and Regulatory Affairs:\nPlan and execute government and third-party procedures to ensure project compliance with US regulations.\nPlan and manage government permits applications.\nProject Management:\nManage technical, quality, safety, and timeline aspects of projects, ensuring timely resolution of technical issues, compliance with quality standards, and implementation of safety measures.\nCoordinate with construction firms, supervisory, and contracting units to manage internal and external project relationships.\nCommissioning and Validation:\nOrganize factory acceptance tests, commissioning, and validation to ensure systems meet user requirements.\nProject Completion:\nLead the final inspection, handover, documentation review, and project settlement activities, ensuring successful project completion and handover.\nReporting and Improvement:\nRegularly report project progress, compile project reports, analyze lessons learned, and suggest improvements.\nQualifications and Requirements\nEducation and Experience:\nBachelor's degree or higher in Mechanical/Electrical, Chemical Engineering, Biomedical Engineering, or related fields.\n10+ years of experience in biopharmaceuticals with substantial project management and facility operations experience.\nHands on experience in managing construction, experience in executing projects from business requirement collection through to design, construction, commissioning, validation, and final settlement is preferred.\nSkills:\nStrong management and reporting capabilities, clear management vision, able to handle high-pressure work environments.\nSolid technical expertise combined with engineering knowledge.\nDemonstrated skills in problem solving, root cause analysis with result driven thought process.\nAdditional Considerations:\nProficient in project management software (e.g., Procore, Microsoft Project, Primavera P6).\nFamiliarity with construction estimating and scheduling tools.\nUnderstanding of US building codes, zoning laws, safety regulations, and biopharmaceutical industry standards.\n#LI-EB1\n#GS\nGenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.\nGenScript USA Inc./ProBio Inc. maintains a drug-free workplace.\n\nPlease note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.","company":"Genscriptprobio","rawCompany":"genscriptprobio","city":"Piscataway","state":"NJ","isRemote":false,"isActive":false,"createdAt":"2026-06-15T04:19:18.304Z","occupations":[{"code":"11-9021.00","title":"Construction Managers","slug":"construction-managers"},{"code":"13-1082.00","title":"Project Management Specialists","slug":"project-management-specialists"},{"code":"47-1011.00","title":"First-Line Supervisors of Construction Trades and Extraction Workers","slug":"first-line-supervisors-of-construction-trades-and-extraction-workers"}],"industries":[{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"236220","title":"Commercial and Institutional Building Construction","slug":"commercial-and-institutional-building-construction"},{"code":"236210","title":"Industrial Building Construction","slug":"industrial-building-construction"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Construction Manager","description":"About GenScript\nGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.\nGenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.\nJob Title: Construction Project Manager\nLocation: Piscataway, NJ (Fully onsite)\nReports to: Director of US Site Operations\nCompensation: The estimated salary range is $120,000 - $150,000, based on experience.\nOverview:\nGenScript is seeking a talented, detail oriented and self-driven individual to join the Operations Department, contributing to the planning, design, construction, commissioning, validation, and engineering process systems development for our facilities in Piscataway, NJ. This position is valid for at least 1-2 years with the opportunity to transition to facility manager after the construction projects are done.\nJob Responsibilities:\nProject Planning and Execution:\nDevelop comprehensive project plans ensuring projects proceed according to set objectives, including requirement gathering, feasibility analysis, risk assessment, and solution formulation.\nManage cost estimation for all project phases and create cost control plans.\nProcurement and Contract Management.\nOversee bidding and procurement for project design, construction, and long-lead equipment.\nManage contract signing and execution with suppliers and contractors, ensuring compliance with terms, quality, and deadlines.\nCompliance and Regulatory Affairs:\nPlan and execute government and third-party procedures to ensure project compliance with US regulations.\nPlan and manage government permits applications.\nProject Management:\nManage technical, quality, safety, and timeline aspects of projects, ensuring timely resolution of technical issues, compliance with quality standards, and implementation of safety measures.\nCoordinate with construction firms, supervisory, and contracting units to manage internal and external project relationships.\nCommissioning and Validation:\nOrganize factory acceptance tests, commissioning, and validation to ensure systems meet user requirements.\nProject Completion:\nLead the final inspection, handover, documentation review, and project settlement activities, ensuring successful project completion and handover.\nReporting and Improvement:\nRegularly report project progress, compile project reports, analyze lessons learned, and suggest improvements.\nQualifications and Requirements\nEducation and Experience:\nBachelor's degree or higher in Mechanical/Electrical, Chemical Engineering, Biomedical Engineering, or related fields.\n10+ years of experience in biopharmaceuticals with substantial project management and facility operations experience.\nHands on experience in managing construction, experience in executing projects from business requirement collection through to design, construction, commissioning, validation, and final settlement is preferred.\nSkills:\nStrong management and reporting capabilities, clear management vision, able to handle high-pressure work environments.\nSolid technical expertise combined with engineering knowledge.\nDemonstrated skills in problem solving, root cause analysis with result driven thought process.\nAdditional Considerations:\nProficient in project management software (e.g., Procore, Microsoft Project, Primavera P6).\nFamiliarity with construction estimating and scheduling tools.\nUnderstanding of US building codes, zoning laws, safety regulations, and biopharmaceutical industry standards.\n#LI-EB1\n#GS\nGenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.\nGenScript USA Inc./ProBio Inc. maintains a drug-free workplace.\n\nPlease note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.","datePosted":"2026-06-15T04:19:18.304Z","dateModified":"2026-06-15T04:19:18.304Z","hiringOrganization":{"@type":"Organization","name":"Genscriptprobio","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Piscataway","addressRegion":"NJ","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"bfee456582dd528de82fba02"},"url":"https://jobsearcher.com/jobs/bfee456582dd528de82fba02"}}