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.
Join a team where innovation meets excellence, and where your expertise will shape the future of biopharmaceutical advancements.