Senior Project Manager, Project Management Office (PMO)
LOTTE Biologics · Syracuse, NY · 1 mo ago
On-siteInformation Technology$91k–$142k/yrFull-time
Duties & Responsibilities
- Lead strategic client‑facing projects from initiation through closeout, ensuring delivery on time, within scope, and within budget.
- Align site PMO objectives with global governance standards, reporting expectations, and best practices.
- Serve as a trusted liaison for clients, internal leadership, and project sponsors, fostering transparency and strong working relationships.
- Develop and manage detailed project plans, identifying critical path activities, key milestones, and strategic intent; ensure stakeholder alignment on expectations and timelines.
- Define project team structure, communicate resource needs, and secure appropriate cross‑functional support.
- Lead all project meetings, including client kickoff, technical transfer, routine team meetings, and vendor coordination.
- Develop and execute project communication strategies, including stakeholder updates and governance reporting.
- Act as the primary point of contact for client communication, scope management, change orders, and performance reporting.
- Proactively identify and resolve project risks and issues; escalate to senior leadership when needed to ensure timely resolution.
- Partner with Manufacturing Operations, Development (MS&T, PD, AS&T), Quality, Supply Chain, and Business Development to support technical transfers, change controls, and business growth.
- Collaborate with Business Development on financial tracking, invoicing, and identifying new opportunities; develop and execute change orders for out‑of‑scope work.
- Manage portfolio‑level resource requirements and coordinate communication across all stakeholder groups.
- Apply PMO frameworks to maintain project metrics, dashboards, timelines, documentation repositories, risk logs, and KPI reporting.
- Support client visits, audits, and Person‑in‑Plant (PIP) activities at the Syracuse site.
- Foster continuous improvement of project management tools, templates, and processes with a focus on safety, quality, schedule, and budget.
- Support non‑client project activities as needed to advance site initiatives.
- Foster diverse, inclusive, high‑performance teams and maintain strong relationships with functional leaders and client representatives.
Education & Experience
- Bachelor’s degree in Engineering, Life Sciences, or a related technical field required.
- 5–10 years of project management experience with demonstrated success influencing and aligning cross‑functional teams within a matrixed organization.
- 3–5 years of experience in the CDMO industry, including leadership of complex cGMP or technical transfer projects.
- PMP or equivalent project management certification preferred.
- Experience managing strategic client relationships preferred.
Knowledge, Skills, & Abilities
- Knowledge of biopharma project management methodologies, risk management practices, and stage‑gate governance.
- Strong understanding of biologics manufacturing processes, analytical and process technical transfer, and regulatory requirements in a GMP environment.
- Strong financial acumen, including purchase order and invoicing processes, cost estimation for scope changes, and accurate tracking of development and manufacturing expenditures (materials, consumables, labor) to support client billing.
- Strong negotiation and stakeholder management skills with the ability to influence across a matrixed organization.
- Proficiency with Microsoft Project, Smartsheet, Power BI, and other project management and data visualization tools.
- Ability to balance strategic thinking with hands‑on project oversight and execution.
- Excellent written, verbal, and presentation skills, with the ability to communicate complex information clearly.
- Strong analytical skills, including data aggregation, interpretation, and presentation.
- Ability to work independently with a high level of accountability and sound judgment.
- Ability to interact effectively with all levels of management and cross‑functional partners.
- Proven ability to manage competing priorities and drive results in a fast‑paced, matrixed environment.
- Excellent customer service skills for servicing as the primary point of contact to customers and representing the entire LOTTE Biologics organization.
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 in Korea and other regions, balancing multiple 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.
Travel
- Mild travel required (less than 5%), primarily for corporate meetings, training, or client visits.
Work Location:
New York Pay Range: $91,000 - $142,000 USD