Global PMO Lead: CAPEX & NPI for Pharma Packaging

Datwyler

Town of Middletown (NY)

Híbrido

USD 130 000 - 170 000

Tempo integral

Há 6 dias
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Resumo da oferta

Datwyler is seeking a PMO Manager to direct CAPEX investments and NPI portfolios across US manufacturing sites (Middletown, DE and Pennsauken, NJ). You will manage the PMO office, oversee 1–5 direct reports, and standardize governance and delivery across services.

The role requires strong project leadership, budgeting and scheduling skills, with deep knowledge of pharmaceutical processes and regulatory requirements.

Qualificações

  • Bachelor's degree in Engineering, Project Management, or related field (Master's degree preferred).
  • Proven experience as a Project Manager in CAPEX projects within the pharmaceutical industry.
  • Strong understanding of pharmaceutical manufacturing processes and regulations.
  • Excellent leadership and communication skills.
  • Ability to manage multiple projects simultaneously.
  • Strong analytical, judgmental and problem solving skills.
  • Great understanding of all financials related to project management such as forecasting, budgeting, cost estimation, building business cases, rigid scope management.
  • Knowledge of complex project management tools (e.g. MS Project).
  • Experience dealing with government agencies and standards in area of expertise.

Responsabilidades

  • Identifies, plans and directs engineering projects and monitors status to ensure timeliness of completion (capital investment, process, quality, continuous improvements and safety)
  • Interacts with key stakeholders to define project scope, goals, and deliverables
  • Derives tasks and resources needed for successful project execution
  • Develops and maintains detailed schedules and project plans
  • Devises and implements recovery strategies for overdue tasks and deliverables
  • Analyzes project critical path and risk assessments to deploy risk mitigation strategies
  • Leads global investment projects for local teams
  • Leads NPI projects for the respective site
  • Develops and manages local investment / capital expenditures (CAPEX) budget
  • Communicates project status to stakeholders and senior management
  • Ensures both sites are compliant with the department's requirements by identifying the requirements (regulatory, corporate, and normative) applicable to the site, in terms of project and transfer and analyzing the gaps and implement appropriate action plans
  • Provides technical support for Operations, Quality , Sales & Technical Services
  • Ensures the implementation of Good Manufacturing Practices (GMP) and the Quality System in its department
  • Develops a department budget and submit it to management for approval & tracking the budget periodically and reassess it on fixed periods by updating assumptions
  • Anticipates the organization of the department based on long-term forecasts, strategic directions of the company and the needs of its customers
  • Establishes the department's dashboards based on information from direct deferrals and analyze departmental indicators to identify deviations or deviations from the guidelines set and/or areas for improvement
  • Consolidates and validates applications related to the CAPEX site
  • Develops and updates the site's master plan for site infrastructure & ensure the study and implementation of engineering projects

Conhecimentos

CAPEX project management
Pharma manufacturing
Leadership
Communication
Budgeting
Scheduling
Risk assessment
Regulatory compliance
MS Project

Formação académica

Bachelor's degree in Engineering or related field
Master's degree preferred

Ferramentas

MS Project

Descrição da oferta de emprego

Datwyler is seeking a PMO Manager to direct CAPEX investments and NPI portfolios across US manufacturing sites (Middletown, DE and Pennsauken, NJ). You will manage the PMO office, oversee 1–5 direct reports, and standardize governance and delivery across services.

The role requires strong project leadership, budgeting and scheduling skills, with deep knowledge of pharmaceutical processes and regulatory requirements.

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