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About GenScript GenScript 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. GenScript 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. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Position Overview:
We are seeking a highly experienced Project Manager to lead the execution of complex gene and cell therapy (GCT) development and manufacturing programs. This role is critical to ensure that cross-functional projects-including plasmid, mRNA, and viral vector platforms-are delivered on time, within scope, and in full compliance with regulatory and quality expectations. The successful candidate will have deep CGT domain knowledge, strong operational leadership, and a strategic mindset to manage internal systems and client-facing execution.
Key Responsibilities: Strategic Project Leadership Lead end-to-end planning and execution of CGT-related programs (e.g., plasmid, mRNA, viral vector) across development and GMP manufacturing phases. Develop and maintain integrated project timelines, resource allocations, and deliverable tracking using tools such as Microsoft Project or Smartsheet. Actively drive internal and client-side alignment across CMC milestones. Stakeholder Engagement & Cross-Functional Collaboration Coordinate across business development, finance, R&D, QA, QC, manufacturing, and regulatory affairs to ensure all project requirements are met. Maintain robust and proactive communication with internal and external stakeholders to ensure alignment, manage expectations, and report progress. Represent project status in executive reviews and client meetings with confidence and professionalism. Operational Oversight & Continuous Improvement Monitor project budget, resource usage, and risk indicators; develop and implement mitigation strategies where needed. Lead issue resolution impacting scope, quality, or timelines. Optimize project management infrastructure, including internal trackers, documentation systems, and SOPs. Qualifications:
Bachelor's degree in life sciences, engineering, or a related technical discipline; advanced degree preferred. Minimum5 years of project management experience in the biopharmaceutical industry, with demonstrated leadership in GMP/CDMO environments. Deep understanding of CGT development lifecycle and regulatory requirements for IND/BLA. Proficiency in Gantt charting, project documentation systems, and PM collaboration tools (e.g., MS Project, SharePoint, MS Teams, Smartsheet). Ability to independently drive cross-functional teams and manage multiple concurrent projects. Strong leadership, communication, and interpersonal skills with a customer-first mindset. Preferred:
PMP (Project Management Professional) certification. Prior experience managing CMC projects involving plasmid, viral vector, or mRNA platforms. Direct experience in a CDMO setting with established track record of external client collaboration. Key Competencies:
Strategic thinking and decision-making under pressure Operational discipline and risk management mindset Excellent client management and negotiation skills Self-driven, positive, and resilient team player The estimated salary range is $120,000 - $160,000, depending on the experience and background.
#PB
#LW
GenScript 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.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please 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
GenScript Biotech Corporation (HK.1548) is an important technology and service provider in the world for life science R&D and manufacture. Built upon its solid DNA synthesis technology, GenScript Biotech comprises four major business units: a life-science services and products business unit, a biologics contract development and manufacturing organization (CDMO) business unit, an industrial synthetic products business unit, and an integrated global cell therapy company.
GenScript Biotech was founded in New Jersey, USA in 2002 and listed on the Hong Kong Stock Exchange in 2015. The company's business operations span over 100 countries and regions worldwide with legal entities located in the U.S., China, Japan, Singapore, Netherlands, Ireland, the United Kingdom, Korea, Belgium and Spain. GenScript Biotech provides premium, convenient and reliable services and products for over 200,000 customers.
As of June 30, 2024, GenScript Biotech had more than 6,900 employees globally, and 103,600 peer-reviewed journal articles worldwide had cited GenScript Biotech's services and products. In addition, GenScript Biotech owns a number of intellectual property rights, including over 300 patents, over 900 patent applications and great numbers of know-how secrets.
Driven by the corporate mission of "make people and nature healthier through biotechnology", GenScript Biotech strives to become the most trustworthy biotech company in the world.
Company info Location Piscataway NJ United States
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About GenScript GenScript 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. GenScript 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. About ProBio ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Position Overview:
We are seeking a highly experienced Project Manager to lead the execution of complex gene and cell therapy (GCT) development and manufacturing programs. This role is critical to ensure that cross-functional projects-including plasmid, mRNA, and viral vector platforms-are delivered on time, within scope, and in full compliance with regulatory and quality expectations. The successful candidate will have deep CGT domain knowledge, strong operational leadership, and a strategic mindset to manage internal systems and client-facing execution.
Key Responsibilities: Strategic Project Leadership Lead end-to-end planning and execution of CGT-related programs (e.g., plasmid, mRNA, viral vector) across development and GMP manufacturing phases. Develop and maintain integrated project timelines, resource allocations, and deliverable tracking using tools such as Microsoft Project or Smartsheet. Actively drive internal and client-side alignment across CMC milestones. Stakeholder Engagement & Cross-Functional Collaboration Coordinate across business development, finance, R&D, QA, QC, manufacturing, and regulatory affairs to ensure all project requirements are met. Maintain robust and proactive communication with internal and external stakeholders to ensure alignment, manage expectations, and report progress. Represent project status in executive reviews and client meetings with confidence and professionalism. Operational Oversight & Continuous Improvement Monitor project budget, resource usage, and risk indicators; develop and implement mitigation strategies where needed. Lead issue resolution impacting scope, quality, or timelines. Optimize project management infrastructure, including internal trackers, documentation systems, and SOPs. Qualifications:
Bachelor's degree in life sciences, engineering, or a related technical discipline; advanced degree preferred. Minimum5 years of project management experience in the biopharmaceutical industry, with demonstrated leadership in GMP/CDMO environments. Deep understanding of CGT development lifecycle and regulatory requirements for IND/BLA. Proficiency in Gantt charting, project documentation systems, and PM collaboration tools (e.g., MS Project, SharePoint, MS Teams, Smartsheet). Ability to independently drive cross-functional teams and manage multiple concurrent projects. Strong leadership, communication, and interpersonal skills with a customer-first mindset. Preferred:
PMP (Project Management Professional) certification. Prior experience managing CMC projects involving plasmid, viral vector, or mRNA platforms. Direct experience in a CDMO setting with established track record of external client collaboration. Key Competencies:
Strategic thinking and decision-making under pressure Operational discipline and risk management mindset Excellent client management and negotiation skills Self-driven, positive, and resilient team player The estimated salary range is $120,000 - $160,000, depending on the experience and background.
#PB
#LW
GenScript 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.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please 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
GenScript Biotech Corporation (HK.1548) is an important technology and service provider in the world for life science R&D and manufacture. Built upon its solid DNA synthesis technology, GenScript Biotech comprises four major business units: a life-science services and products business unit, a biologics contract development and manufacturing organization (CDMO) business unit, an industrial synthetic products business unit, and an integrated global cell therapy company.
GenScript Biotech was founded in New Jersey, USA in 2002 and listed on the Hong Kong Stock Exchange in 2015. The company's business operations span over 100 countries and regions worldwide with legal entities located in the U.S., China, Japan, Singapore, Netherlands, Ireland, the United Kingdom, Korea, Belgium and Spain. GenScript Biotech provides premium, convenient and reliable services and products for over 200,000 customers.
As of June 30, 2024, GenScript Biotech had more than 6,900 employees globally, and 103,600 peer-reviewed journal articles worldwide had cited GenScript Biotech's services and products. In addition, GenScript Biotech owns a number of intellectual property rights, including over 300 patents, over 900 patent applications and great numbers of know-how secrets.
Driven by the corporate mission of "make people and nature healthier through biotechnology", GenScript Biotech strives to become the most trustworthy biotech company in the world.
Company info Location Piscataway NJ United States
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