Project Manager (CDMO Manufacturing)

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.