Director, Project Management Office (PMO)

Posted 4 Days Ago
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Syracuse, NY, USA
In-Office
155K-220K Annually
Expert/Leader
Healthtech • Pharmaceutical
Delivering Manufacturing Excellence
The Role
Lead the Syracuse site PMO to establish governance, portfolio management, and delivery disciplines for complex biologics CDMO programs. Oversee project execution, financial oversight, client relationships, risk management, resource planning, and PMO capability building while partnering with global PMO and site leadership to drive predictable, high-quality program delivery.
Summary Generated by Built In

We are LOTTE BIOLOGICS! Delivering Therapies That Enable a Healthier World

A new company, built on 80 years of tradition. We embody our core values of being Inspired by Science, Embracing Diversity, Fostering Talent, and Connecting Lives. Our mission is to be the most trusted partner in the industry, with high standards of quality and continuous innovation, to reliably deliver benefits for patients worldwide. 

Position Summary

The Director, Project Management Office (PMO) is responsible for leading the PMO function for the Syracuse Bio Campus and ensuring effective portfolio governance, project execution, and cross-functional alignment across client programs and strategic internal initiatives. This role establishes and drives PMO operating standards, governance processes, performance metrics, and execution disciplines that enable visibility, predictability, and delivery excellence across the project portfolio.

As a senior leader within the site and a key member of the Global PMO network, this role translates site and business priorities into PMO strategy, governance, and execution frameworks that support operational performance, client satisfaction, and business growth. The Director serves as a strategic business partner to site leadership and a senior point of contact for clients, providing leadership across Manufacturing Operations, Development (PD, AS&T), MSAT, Quality, Supply Chain, Finance, and Business Development to drive outcomes across complex biologics programs.

The ideal candidate brings deep experience in biologics and CDMO operations, strong business and financial acumen, and demonstrated success leading project management organizations, complex technical transfer and cGMP programs, and cross-functional teams in a matrixed environment.

Duties & Responsibilities

Leadership & Strategy

  • Lead the PMO function for the Syracuse Bio Campus, including functional priorities, governance standards, operating mechanisms, and talent development.
  • Translate site, functional, and business objectives into PMO strategies, priorities, and execution frameworks that support successful delivery of client programs and internal strategic initiatives.
  • Partner with the VP, Global PMO to align site PMO objectives with global PMO strategy, governance standards, reporting expectations, and continuous improvement priorities.
  • Establish and sustain PMO frameworks, processes, tools, and performance measures that improve consistency, transparency, predictability, and decision-making across the project portfolio.
  • Serve as a strategic partner to site leadership, helping to identify risks, opportunities, resource needs, and operational tradeoffs that impact project delivery and business performance.
  • Influence and help shape PMO best practices across the broader global network through active partnership, knowledge sharing, and adoption of scalable standards.

Project Oversight & Governance

  • Provide leadership and oversight for the execution of Syracuse client projects and key internal initiatives, ensuring delivery against scope, timelines, financial commitments, quality requirements, and customer expectations.
  • Direct portfolio governance processes, including project reviews, milestone assessments, escalation management, portfolio reporting, and decision-support mechanisms for site and global leadership.
  • Ensure risk management, issue escalation, and mitigation planning are embedded within project execution and aligned across cross-functional stakeholders.
  • Drive portfolio visibility through clear governance, KPI reporting, lessons learned, and performance reviews that support timely and effective decision-making.
  • Lead PMO engagement in the planning and execution of complex client-facing programs, including end-to-end CDMO projects involving cell line development, linker-payload, drug substance, drug product, and technical transfer activities as applicable.
  • Identify and implement improvements to PMO effectiveness, including governance, reporting, prioritization, resource planning, and organizational capability.

Client Relationship Management

  • Serve as a senior PMO representative and trusted liaison for client stakeholders, ensuring strong communication, transparency, responsiveness, and alignment throughout the project lifecycle.
  • Lead or participate in Joint Steering Committee (JSC) meetings and other governance forums with clients, providing clear updates on program status, risks, financials, scope changes, and milestones.
  • Partner closely with Business Development, Development, and Operations to support new business opportunities, project onboarding, technical transfers, change controls, and ongoing client program success.
  • Ensure project scope, change order management, and program communications are managed effectively and in alignment with contractual, operational, and financial objectives.
  • Support business growth by helping to create delivery models, governance approaches, and cross-functional plans that enable successful execution of new and expanding client programs.

Financial & Operational Accountability

  • Lead PMO financial oversight for client programs and the function, including forecasting, budget management, invoicing alignment, change impact visibility, and cost control.
  • Provide site and senior leadership with clear visibility to project financials, milestones, risks, constraints, and operational implications.
  • Partner with site leadership and cross-functional stakeholders on strategic capacity planning, prioritization, and resource allocation to support portfolio execution and business commitments.
  • Drive operational discipline and accountability across the PMO by linking project performance to business, financial, and customer outcomes.
  • Support the resolution of highly complex project and portfolio challenges by coordinating across functions, balancing competing priorities, and identifying pragmatic solutions.

People & Culture

  • Lead, develop, and coach a team of project managers responsible for client project execution at the Syracuse Bio Campus.
  • Set clear expectations, performance standards, and development priorities for the PMO team to ensure high levels of accountability, engagement, and effectiveness.
  • Build PMO organizational capability through mentoring, succession planning, knowledge sharing, and continuous professional development.
  • Foster a high-performing team culture grounded in collaboration, inclusion, ownership, client focus, and continuous improvement.
  • Lead through both direct people management and matrix influence to align teams, resolve conflict, and drive execution across functions and stakeholders.

Education & Experience

  • Bachelor’s degree in Engineering, Life Sciences, Business, or a related field required; advanced degree preferred.
  • Requires 12+ years of relevant experience, including significant experience in the biopharma and/or CDMO industry.
  • Significant leadership experience in project management, program/alliance management, PMO leadership, and/or related operational leadership roles supporting complex biologics programs.
  • Demonstrated success leading complex cGMP manufacturing, technical transfer, and/or end-to-end client programs within a contract development and manufacturing environment.
  • Proven experience establishing, leading, or enhancing PMO governance frameworks, portfolio management processes, and performance reporting mechanisms.
  • Experience leading direct reports and developing talent within a matrixed, cross-functional organization.
  • Demonstrated success influencing senior leaders, clients, and cross-functional stakeholders to drive decisions, alignment, and business outcomes.
  • Strong experience managing client relationships, governance forums, and complex project communications at a strategic level.
  • PMP (Project Management Professional) or equivalent certification preferred.

Knowledge, Skills, Abilities

  • Deep knowledge of project and portfolio management methodologies, risk management practices, and governance models within a biopharmaceutical or CDMO environment.
  • Strong understanding of biologics manufacturing, process and analytical technical transfer, cGMP operations, and regulatory requirements in GxP settings.
  • Strong business and financial acumen, including understanding of project forecasting, cost management, invoicing processes, change impact assessment, and client financial visibility.
  • Ability to translate business strategy and operational priorities into PMO governance, execution plans, and measurable outcomes.
  • Demonstrated ability to influence senior leaders, clients, and cross-functional stakeholders across a matrixed organization.
  • Strong people leadership skills, including coaching, performance management, organizational development, and capability building.
  • Ability to lead through ambiguity, manage competing priorities, and drive resolution of complex operational and portfolio issues.
  • Excellent communication, presentation, negotiation, and stakeholder management skills, including executive-level communication.
  • Proficiency with Microsoft Project, Smartsheet, Power BI, and other project and portfolio management tools.
  • Ability to balance strategic leadership with appropriate operational involvement to support execution and business outcomes.

Physical Demands

  • Prolonged periods of sitting or standing at a desk, participating in meetings, and working on a computer.
  • Frequent use of standard office equipment (computers, monitors, telephones, printers, projectors).
  • Occasional movement throughout the site to attend meetings, observe project activities, or interface with operations teams in manufacturing or laboratory areas.
  • Ability to wear required personal protective equipment (PPE) when entering controlled manufacturing or lab environments (e.g., safety glasses, lab coats, shoe covers).
  • Visual acuity to review project data, timelines, and technical documentation in both electronic and printed formats.
  • Occasional lifting or carrying of materials (up to 15 lbs.), such as binders, laptops, or presentation materials.

Work Environment

  • Onsite role based at the Syracuse Bio Campus (cGMP manufacturing facility), requiring regular presence and engagement with cross-functional teams.
  • Partner closely with global counterparts across regions and time zones to maintain clear communication and alignment across projects.
  • Work is primarily performed in an open or shared office environment, requiring a high degree of collaboration, communication, and adaptability.
  • Frequent interaction with internal departments (Manufacturing, Development, Quality, Supply Chain, Finance, Business Development) and external clients.
  • Occasional entry into GMP manufacturing and laboratory spaces, which requires adherence to gowning and safety procedures.
  • May involve extended hours or flexibility during critical project phases, client audits, or leadership meetings.

Supervisory Responsibilities 

  • Leads, develops, and manages PMO team members, including hiring, performance management, and coaching.
  • Oversees resource planning and allocation to ensure effective program and project delivery.
  • Establishes clear goals, accountability, and performance expectations aligned to organizational priorities.
  • Promotes a high-performing, collaborative team culture and adoption of PMO standards and best practices.
  • Provides guidance and mentorship to strengthen project management capabilities across the organization.

Travel

  • Up to 10–15% travel for client meetings, global PMO forums, training, client site visits or cross-site/corporate meeting collaboration.

Target Bonus

23%

Work Location:

East Syracuse, NY

New York Pay Range
$155,000$220,000 USD

We are an Equal Employment Opportunity (“EEO”) Employer. 

We believe that women, people of color, veterans and LGBTQ communities must participate in the work we do, so we strongly encourage applications from people with these identities or who are members of underrepresented communities!  If this is the work that you want to do, in a culture of inclusion and excellence with the goal of making our world to be a healthier place, then please apply today! 


Skills Required

  • Bachelor's degree in Engineering, Life Sciences, Business, or related field
  • Advanced degree
  • 12+ years of relevant experience, including biopharma and/or CDMO industry experience
  • Significant leadership experience in project management, program/alliance management or PMO leadership
  • Demonstrated success leading complex cGMP manufacturing, technical transfer, and end-to-end client programs
  • Proven experience establishing or enhancing PMO governance, portfolio management processes, and reporting
  • Experience leading direct reports and developing talent in a matrixed, cross-functional organization
  • Strong experience managing client relationships, governance forums, and strategic project communications
  • Strong business and financial acumen, including forecasting, budget management, invoicing alignment and change impact assessment
  • Proficiency with Microsoft Project, Smartsheet, Power BI or similar project and portfolio management tools
  • PMP or equivalent certification
  • Onsite presence at Syracuse Bio Campus and ability to enter GMP manufacturing and lab environments (PPE compliance)
  • Ability to travel up to 10-15% for client and global PMO meetings
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The Company
HQ: Seoul
522 Employees
Year Founded: 2022

What We Do

Headquartered in Seoul, South Korea, LOTTE BIOLOGICS was founded in 2022 with a mission to deliver therapies that contribute to a healthier world. At the Syracuse Bio Campus in New York, LOTTE BIOLOGICS provides high-quality GMP manufacturing services for drug substances. The facility offers a total production capacity of 40,000L, supported by eight 5,000L stainless steel bioreactors. Additionally, the campus includes extensive analytical QC testing laboratories and warehouse facilities that have received over 62 regulatory approvals from agencies worldwide. LOTTE BIOLOGICS is also advancing into a new area of expertise with Antibody-Drug Conjugates (ADCs) services. With over $100 million invested in ADC modalities, including both drug substance and conjugation capabilities on-site, we offer a seamless, end-to-end service from drug substance manufacturing to conjugation. Looking ahead, LOTTE BIOLOGICS is constructing three advanced bio plants in Songdo, South Korea. With construction of the first plant already underway and expected to be operational by 2027, each facility will feature eight 15,000L stainless steel bioreactors for large-scale commercial production, along with multiple 3,000L bioreactors to meet clinical production needs. Collectively, these plants will provide a manufacturing volume exceeding 360,000L in bioreactor capacity. Through our commitment to delivering innovative medicines to patients worldwide, LOTTE BIOLOGICS aims to become a top-tier global CDMO company in the biopharmaceutical industry.

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