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ProBio

Biologics and CGT CDMO platform

Facility Project Manager

Construction ManagementUpdated on Nov 12
Full-timePennington, NJ, USAIn-person

About the Job

Requirements

  • A Bachelor’s or advanced degree in Construction Management, Mechanical Engineering, Biomedical Engineering, or another engineering capacity is required.
  • Strength in managing facility and construction projects for facilities in the pharmaceutical industry is required.
  • Experience in project management and engineering practices is required.
  • Familiarity with estimating and bidding is required.
  • Experience negotiating with landlords, government regulation offices, and engineering and construction contractors is required.
  • Understanding of manufacturing processes for plasmid DNA and viral vectors in the cell and gene therapy industry is required.
  • Proficiency in AutoCAD and Microsoft Project is highly desired.

Responsibilities

  • Coordinate and oversee facility outside services, engineering, and construction capital projects for GXP and non-GMP facilities in New Jersey.
  • Manage multiple facility outside-services, engineering, and construction projects ranging from $0.05 million to $30 million at any given time.
  • Direct day-to-day project-team activities and track action items throughout each project lifecycle.
  • Bid, award, and select engineering firms, construction firms, equipment vendors, commissioning, qualification, and validation consultants, and service contractors.
  • Ensure user requirement specifications are met through high-quality project deliverables.
  • Develop and maintain project schedules to foster accountability and identify staffing requirements.
  • Manage project capital budgets to support on-time, under-budget completion, and ensure purchase orders and contracts meet budget and company standards.
  • Review and process change orders in accordance with contract requirements.
  • Prepare project updates and budget-release presentations for upper management teams.
  • Build partnering relationships with project executives, landlords, contractors, and consultants.
  • Host Gemba walks and track correction of observations to support continuous site improvement.
  • Execute and manage the site-wide controlled-drawings program, including physical verification, redlining, correction, and control of drawings required for qualification activities.
  • Establish and maintain the site security program, assign new badges, control security clearances, and rectify security incidents.

Desired Qualifications

  • PMP or a similar project-management certification is preferred.

About the Company

ProBio

Biologics and CGT CDMO platform

ProBio (GenScript ProBio) is a biologics and cell/gene therapy CDMO platform that offers end-to-end services from antibody and protein discovery through commercial manufacturing, plus plasmid, viral vector, and mRNA CMC services. It operates GMP-capable facilities in China and the United States and has supported 100+ IND filings for global clients since 2017. The company, spun from GenScript, provides a full suite of development and manufacturing options, enabling clients to move products from discovery to market readiness. Unlike many single-solution providers, ProBio covers the entire spectrum of biologics and CGT workflows in-house, with multi-region GMP capacity and a track record of regulatory support. Its goal is to help customers bring biologics and gene-therapy products to clinical trials and commercial production by offering integrated, globally accessible CDMO services.

Company size
Not listed
Company stage
Not listed
Total funding
Not listed
Headquarters
Nanjing City, China
Founded
2017

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