Director, Program Management
Watertown, NY - USA
Job Summary
We are seeking an experienced driven and collaborative Director of Program Management to lead the execution of complex cross-functional client programs in the development and GMP manufacturing of cell and gene therapies. This leader will be responsible for driving program success across multiple client engagements and ensuring alignment with strategic and operational goals.
This role requires deep understanding of GMP operations program and stakeholder management and the ability to lead both internal teams and external clients with clarity confidence and accountability.
- Lead and oversee multiple complex cross-functional client programs from contract award through closure ensuring on-time on-budget and on-scope delivery.
- Own the client relationship for assigned programs; serve as the main point of contact and ensure program health transparency and trust with both internal and external stakeholders.
- Develop and maintain program documentation including charters timelines risk registers change orders budgets meeting minutes and stakeholder reports.
- Drive strategic alignment between program objectives and broader business goals; contribute to long-term planning client development and organizational strategy.
- Collaborate cross-functionally with Process & Analytical Development Quality GMP Manufacturing Supply Chain Facilities Engineering Quality Control and Regulatory to deliver program milestones.
- Identify and manage program risks through proactive mitigation planning and structured risk management frameworks.
- Track and report on key performance indicators (KPIs) such as delivery timelines client satisfaction quality metrics and budget adherence.
- Lead program steering committees and governance forums; prepare executive-level presentations and reports for internal and client leadership.
- Contribute to the development of scalable PMO tools and frameworks including Smartsheet dashboards process maps and templates.
- Champion process improvements lead root-cause analyses for program deviations and contribute to organizational learning and maturity.
- BA/BS degree in a relevant field required; advanced degree (MS MBA PhD) is a plus.
- 10 years of program or project management experience in life sciences with at least 5 years leading cross-functional programs in GMP manufacturing of cell gene or biologic therapies.
- Proven ability to lead client-facing engagements manage complex stakeholders and resolve cross-functional conflicts.
- 3 years of people management experience including direct reports and matrixed team leadership preferred.
- Deep understanding of GMP principles and regulated development environments.
- PMP certification or equivalent is preferred.
- Strong knowledge of project management tools and systems including Smartsheet Microsoft Project and PowerPoint.
- Demonstrated financial acumen including budget tracking and change order management.
- Experience working in a matrixed fast-paced and early-stage environment is a plus.
Ideal Candidate Attributes:
- Strategic thinker with excellent execution discipline
- Exceptional communicator and relationship builder
- High emotional intelligence and leadership presence
- Comfortable with ambiguity change and problem-solving
- Passionate about improving human health through scientific innovation
Landmark Bio is an Equal Opportunity Affirmative Action employer. Minorities women veterans and individuals with disabilities are encouraged to apply.
Required Experience:
Director
About Company
Landmark Bio is dedicated to translating cutting-edge research into life-changing therapies. The company provides CMC development and GMP manufacturing capabilities for cell and gene therapies and other novel modalities, and partners with academic, biotech, and industry collaborators ... View more