Biotech Project Manager – Client Delivery

Resilience; Olde West Chester (OH); On-site; USD 80,000 - 121,000; Full time

Benefits offered by this job

Annual bonus

401(k) match

Healthcare benefits

Paid vacation

Paid holidays

Tuition reimbursement

Caregiving support

Life & disability insurance

Paid leaves of absence

Job summary

Resilience is seeking a Project Manager I in Ohio to coordinate client projects within a CDMO. You will develop plans, track schedules, and keep cross-functional teams aligned to meet milestones and deliverables.

The role emphasizes risk management, client communication, and collaboration across manufacturing, quality, regulatory, and development functions to support successful drug programs.

Qualifications

• Previous experience coordinating projects in biotechnology, pharma, CDMO, or related industries.
• Understanding of pharmaceutical manufacturing processes and GMP requirements.
• Strong organizational, communication, and stakeholder management skills.
• Experience using project management tools such as Microsoft Project or Smartsheet.
• Ability to manage multiple priorities in a fast-paced environment.

Responsibilities

• Manage assigned client projects from initiation through completion.
• Develop and maintain project timelines, action item logs, and status reports.
• Coordinate project activities across Manufacturing, Quality, Supply Chain, MS&T, Regulatory Affairs, and Product Development.
• Ensure deliverables meet timelines and scope; support technical transfer and manufacturing readiness.
• Serve as day-to-day client contact and provide project status updates.
• Escalate issues, risks, and resource constraints as needed.

Skills

Project coordination

Cross-functional collaboration

GMP knowledge

Communication

Organizational skills

Education

Bachelor’s degree in Life Sciences / Engineering / Pharmaceutical Sciences / Business

PMP certification

Tools

Microsoft Project

Smartsheet

Job description

Resilience is seeking a Project Manager I in Ohio to coordinate client projects within a CDMO. You will develop plans, track schedules, and keep cross-functional teams aligned to meet milestones and deliverables.

The role emphasizes risk management, client communication, and collaboration across manufacturing, quality, regulatory, and development functions to support successful drug programs.