Senior Manager, Project Manager - Biologics

Senior Manager, Project Management The Senior Manager, Project Management will manage and support the initiation, planning, and execution of complex, multi‑disciplinary projects throughout Devens Biologics. The role requires extensive professional experience in the Pharma/Biotech regulated environment and proficiency in PMI program management standards and PMO best practices. Responsibilities Understand and align business strategy and processes with project objectives. Identify technical solutions and partner with process owners and suppliers. Partner with the Devens Biologics Operations Leadership Team and project sponsors for successful delivery. Schedule governance/steering committee meetings and prepare materials. Facilitate project meetings and document decisions. Apply project management expertise across the portfolio, managing multiple workstreams concurrently. Define project scope, goals, deliverables, budget, and timeline. Develop work breakdown structures (WBS) and Agile sprint plans. Manage WBS in a Project Portfolio Management system (OnePlan) or MS‑Project. Sequence activities, estimate resources and durations, and plan resources for the program. Develop critical‑path analyses and identify risks and opportunities. Monitor project performance ensuring completion of short‑ and long‑term goals. Conduct qualitative and quantitative risk analysis and implement mitigation plans. Maintain program budgets and adjust constraints based on financial analysis. Create and communicate project plans, dependencies, milestones, and deliverables. Manage project schedules and proactively communicate upcoming activities to steering committees and leads. Use change management methods to mitigate barriers to improvement. Escalate concerns to the Associate Director of PMO or site leadership when required. Develop action or contingency plans for project‑related issues and risks. Prepare and present business cases and status updates to leadership and steering committees. Lead large cross‑functional projects independently and evaluate outcomes. Serve as the primary point of contact for all project‑related communications. Qualifications 8+ years of program/project management experience in GxP biopharmaceutical environments. Proven track record in production and/or manufacturing operations. Strong understanding of GMP and FDA regulatory requirements for biologics. PMP certification required. Agile / Scrum Master certification and Change Management certification are pluses. Experience with Lean and Continuous Improvement practices. Knowledge of performance measurement tools and metrics. Experience with project standard methodologies: Waterfall, Agile, Hybrid, SDLC. Advanced degree in Science/Engineering/Business is a plus. Expertise in conflict resolution, facilitation, change management, and interpersonal skills. Strong analytical, problem‑solving, and financial acumen. Excellent communication skills; ability to influence cross‑functional stakeholders. Operationally focused with high organization and self‑starter mindset. Ability to manage details while maintaining a big‑picture view. Compensation Devens – MA – US: $135,200 – $163,832 annually. Compensation may include additional incentive cash and stock opportunities. Final pay is determined based on experience and qualifications. Benefits Health coverage: medical, pharmacy, dental, and vision. Well‑being programs (Well‑Being Account, Living Life Better, Employee Assistance Programs). 401(k) plan, disability, life and accident insurance, supplemental health insurance, travel protection. Paid time off; flexible time off, paid holidays, paid sick time, volunteer days, summer hours flexibility, leaves of absence. Global shutdown period from Christmas to New Year’s Day. Other benefits available as per location; see for details. EEO Statement We are an Equal Opportunity Employer. For our full Equal Employment Opportunity statement, see #J-18808-Ljbffr