{"schemaVersion":"jobsearcher.job.v1","id":"fadea3386e15b6c85cb70721","url":"https://jobsearcher.com/jobs/fadea3386e15b6c85cb70721","canonicalUrl":"https://jobsearcher.com/jobs/fadea3386e15b6c85cb70721","title":"Project Manager","description":"About the Role:Our client, a leading gene therapy Contract Development and Manufacturing Organization (CDMO) specializing in viral vector process and analytical development, is seeking an experienced Program Manager. This role involves overseeing multiple cross-functional projects within Process Development, Analytical Development, Quality Control, and Operations teams, ensuring seamless integration and successful project delivery.Key Responsibilities:Project Leadership: Independently lead and manage at least 4 projects simultaneously, ensuring on-time, on-budget delivery.Planning & Scheduling: Develop and maintain RAID Logs and Gantt charts; monitor and track activities associated with budgets, invoicing, timelines, scope, alignment, and priorities.Cross-Functional Collaboration: Work closely with non-GMP teams, including Process Development, Analytical Development, Quality Control, and Operations, to ensure project success.Communication: Serve as the primary point of contact for internal and external stakeholders, providing regular updates and addressing any issues promptly.Technical Requirements:Bachelor's degree in a relevant field.Minimum of 5 years of experience in biotech/pharmaceutical cross-functional team program or project management.Direct experience in a CDMO environment or strong external manufacturing project management experience with sponsor companies.Proficiency in Microsoft Office Suite and project management software (e.g., Smartsheet).Excellent communication, interpersonal, negotiation, and business skills.Preferred Qualifications:Experience with Adeno-associated virus (AAV) vectors, biologics, or gene therapy.Prior laboratory or scientific/research background.","company":"S4 Analytics","rawCompany":"s4 analytics","city":"Columbus","state":"OH","isRemote":false,"isActive":false,"createdAt":"2026-04-12T19:25:33.941Z","occupations":[{"code":"13-1082.00","title":"Project Management Specialists","slug":"project-management-specialists"},{"code":"11-9021.00","title":"Construction Managers","slug":"construction-managers"},{"code":"15-1299.09","title":"Information Technology Project Managers","slug":"information-technology-project-managers"}],"industries":[{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Project Manager","description":"About the Role:Our client, a leading gene therapy Contract Development and Manufacturing Organization (CDMO) specializing in viral vector process and analytical development, is seeking an experienced Program Manager. This role involves overseeing multiple cross-functional projects within Process Development, Analytical Development, Quality Control, and Operations teams, ensuring seamless integration and successful project delivery.Key Responsibilities:Project Leadership: Independently lead and manage at least 4 projects simultaneously, ensuring on-time, on-budget delivery.Planning & Scheduling: Develop and maintain RAID Logs and Gantt charts; monitor and track activities associated with budgets, invoicing, timelines, scope, alignment, and priorities.Cross-Functional Collaboration: Work closely with non-GMP teams, including Process Development, Analytical Development, Quality Control, and Operations, to ensure project success.Communication: Serve as the primary point of contact for internal and external stakeholders, providing regular updates and addressing any issues promptly.Technical Requirements:Bachelor's degree in a relevant field.Minimum of 5 years of experience in biotech/pharmaceutical cross-functional team program or project management.Direct experience in a CDMO environment or strong external manufacturing project management experience with sponsor companies.Proficiency in Microsoft Office Suite and project management software (e.g., Smartsheet).Excellent communication, interpersonal, negotiation, and business skills.Preferred Qualifications:Experience with Adeno-associated virus (AAV) vectors, biologics, or gene therapy.Prior laboratory or scientific/research background.","datePosted":"2026-04-12T19:25:33.941Z","dateModified":"2026-04-12T19:25:33.941Z","hiringOrganization":{"@type":"Organization","name":"S4 Analytics","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Columbus","addressRegion":"OH","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"fadea3386e15b6c85cb70721"},"url":"https://jobsearcher.com/jobs/fadea3386e15b6c85cb70721"}}