BioSpace, Inc.
Overview
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Principal Project Manager CGT
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BioSpace The original posting includes details about GenScript GenScript Biotech Corporation and ProBio; for the purpose of this refined description, focus remains on the Principal Project Manager CGT role and its responsibilities and qualifications. 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 projectsincluding plasmid, mRNA, and viral vector platformsare 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
Bachelors degree in life sciences, engineering, or a related technical discipline; advanced degree preferred. Minimum 5 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. 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. #J-18808-Ljbffr
Join to apply for the
Principal Project Manager CGT
role at
BioSpace The original posting includes details about GenScript GenScript Biotech Corporation and ProBio; for the purpose of this refined description, focus remains on the Principal Project Manager CGT role and its responsibilities and qualifications. 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 projectsincluding plasmid, mRNA, and viral vector platformsare 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
Bachelors degree in life sciences, engineering, or a related technical discipline; advanced degree preferred. Minimum 5 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. 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. #J-18808-Ljbffr