Biotech CDMO: Project Manager I

Resilience

Port Union (OH)

On-site

USD 80,000 - 121,000

Full time

6 days ago
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Benefits offered by this job

Annual bonus
401(k) with company match
Comprehensive benefits

Job summary

Resilience, a technology-focused biomanufacturing company, is hiring a Project Manager I to coordinate client projects within a CDMO setting. You will manage timelines, deliverables, and cross-functional collaboration across manufacturing, quality, supply chain, MS&T, regulatory, and product development teams.

You will serve as the primary client contact for assigned programs, facilitate meetings, communicate progress and risks, and support technical transfer and manufacturing readiness while

Qualifications

  • Previous experience coordinating projects in biotech, pharma, CDMO or related industries.
  • Understanding of pharmaceutical manufacturing processes and GMP requirements.
  • Strong organizational, communication, and stakeholder management skills.
  • Experience with project management tools (MS Project, Smartsheet) or equivalent.
  • Ability to manage multiple priorities in a fast-paced environment.

Responsibilities

  • Coordinate client projects from initiation through completion.
  • Develop and maintain project timelines, action logs, and status reports.
  • Coordinate activities across Manufacturing, Quality, Supply Chain, MS&T, Regulatory Affairs, and Product Development.
  • Support technical transfer and manufacturing readiness activities.
  • Manage project budgets, change orders, and scope changes.

Skills

Project management
Communication
Stakeholder management
Organizational skills
GMP knowledge
PM tools

Education

Bachelor's degree in Life Sciences, Engineering, Pharmaceutical Sciences, Business, or related discipline

Tools

Microsoft Project
Smartsheet

Job description

Resilience, a technology-focused biomanufacturing company, is hiring a Project Manager I to coordinate client projects within a CDMO setting. You will manage timelines, deliverables, and cross-functional collaboration across manufacturing, quality, supply chain, MS&T, regulatory, and product development teams.

You will serve as the primary client contact for assigned programs, facilitate meetings, communicate progress and risks, and support technical transfer and manufacturing readiness while

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