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Project Manager (CDMO Manufacturing)

Pharma Universe

N/A


Job Details

Full-time


Full Job Description

Project Manager, Biologics CDMO

Location: On-site, USA - Pennsylvania (relocation assistance for non-local candidates is available)

Type: Full-time

Are you a skilled project manager with a passion for driving cutting-edge biopharmaceutical development projects? We’re seeking an experienced Project Manager to join a leading Biologics CDMO. This role offers the opportunity to work on groundbreaking programs, including Chemistry, Bioconjugation Development, and manufacturing, while collaborating with global clients and multidisciplinary teams.

Key Responsibilities:

  • Manage integrated development programs, ensuring alignment with client goals and company standards.
  • Develop and oversee project plans, tracking milestones, budgets, and schedules.
  • Communicate progress, changes, and plans to both clients and internal stakeholders.
  • Facilitate risk assessment and mitigation strategies.
  • Lead project kick-off meetings, create agendas, and document outcomes.
  • Oversee project budgets, ensuring cost control, revenue recognition, and accurate forecasting.
  • Support client relationships by maintaining transparent communication and fostering collaboration.
  • Mentor and guide team members to strengthen the project management organization.
  • Drive initiatives to improve project management processes.

What You’ll Bring:

  • Master’s degree in Life Sciences, Engineering, or a related field.
  • 4+ years of project management experience in a client-facing role, with 2+ years in the CDMO sector.
  • Expertise in CMC, including process development, regulatory requirements, and analytical development.
  • Proficiency with Microsoft Project and a demonstrated ability to manage multiple complex projects.
  • Strong adaptability, accountability, and a solutions-focused approach to challenges.
  • Availability to work on-site 5 days a week and collaborate with clients across various time zones.

Preferred Qualifications:

  • Experience in small molecules or antibody-drug conjugates is a plus.

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