Sr Project Manager, Site Project Management Office

Sr Project Manager, Site Project Management Office Employer LOTTE BIOLOGICS USA LLC Location Syracuse, New York Salary Pay Transparency: $91,000 - $142,000; Competitive Benefits Package; 401k Match; 16% Target Bonus; Relocation support Start date May 29, 2026 View more categories View less categories Discipline Engineering , Biomedical Engineer , Chemical Engineer , Mechanical/Manufacturing Engineer , Process Engineer , Manufacturing & Production , Manufacturing/Mechanical , Process , Science/R D , Biology , Biotechnology , Chemistry Required Education Bachelors Degree Position Type Full time Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details Position Summary The Sr. Project Manager, Site PMO, leads cross-functional clientfacing and internal initiatives and influences how the site executes strategic and operational priorities. This role drives project delivery excellence and establishes and embeds project management best practices. The Sr. Project Manager maintains project governance tools including metrics, dashboards, and performance reports., and uses these insights to influence decisionmaking at governance meetings. The Sr. Project Manager ensures alignment across Manufacturing Operations, Development (MS&T, PD, AS&T), Quality, Supply Chain, and Business Development. The individual anticipates organizational needs, identifies interdependencies, and proactively guides teams toward solutions that support longterm site objectives. As a trusted liaison for clients, the Sr. Project Manager fosters strong relationships, ensures transparency, and upholds accountability throughout the project lifecycle. Duties & Responsibilities Lead strategic clientfacing 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 crossfunctional 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 outofscope work. Manage portfoliolevel 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 PersoninPlant (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 nonclient project activities as needed to advance site initiatives. Foster diverse, inclusive, highperformance 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 crossfunctional 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 stagegate 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 handson 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 crossfunctional partners. Proven ability to manage competing priorities and drive results in a fastpaced, 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 Minimal travel required (less than 5%), primarily for corporate meetings, training, or client visits. Target Bonus 16% Work Location: East Syracuse, NY Share this job Facebook Twitter LinkedIn Apply now Send job Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert