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Manager, PMO - Project Controls

Novo Nordisk
Full-time
On-site
Clayton, NC
Operations

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Role Summary

Manager, PMO - Project Controls. Direct and coordinate the activities of the Project Controls Team in support of the Site Clayton Project Office at Novo Nordisk to meet and/or exceed business, regulatory and customer requirements in accordance with the Novo Nordisk Way. This includes providing direction, coaching, management and supervision of team members, internal and external contractors.

Responsibilities

  • Support Site projects, drive key investment portfolio projects and related programs
  • Establish operational project controls (change, risk, schedule, documentation) for all projects within the Site and associated systems
  • Oversee the efficient and proactive management of the Site Project Portfolio of capital investments and non-capital projects
  • Manage internal and external project services with risk-based decision-making to balance scope, schedule, and cost
  • Facilitate executive stakeholder management and communication for quick decision-making and resolution
  • Drive site program scheduling and resources allocation
  • Ensure cost controls are in place and function in accordance with budget and in compliance with all regulatory requirements in collaboration with the Accounting and Finance team
  • Manage change and risk management processes for the Site Project Office
  • Oversee engineering document control within project phases, aligning with NN standards for documentation control and systems
  • Support program governance and relations with NN teams to establish transparency and alignment regarding project execution
  • Follow all safety and environmental requirements in the performance of duties
  • Other accountabilities, as assigned

Qualifications

  • Bachelor’s degree in science, engineering, business or related field of study from an accredited university required
  • Master’s degree in science, engineering or business preferred
  • Minimum of seven (7) years of project management or consultancy required
  • Minimum of three (3) years of leadership experience required
  • Minimum of seven (7) years of project management or consultancy required
  • Minimum of seven (7) years of experience in manufacturing, engineering, or quality, preferably in a pharmaceutical or other regulated industry required
  • Knowledgeable in systems within pharmaceutical industries to include parenteral drug production preferred
  • Knowledgeable in the effective management required when working in complex organizations and in managing contractors to achieve project goals required
  • Knowledge of large CAPEX projects with focus on PMI/Novo Nordisk project management governance a plus
  • Excellent verbal and written communication skills required
  • Proven expertise in mentoring/development, change management, planning/organizing, managing execution

Skills

  • Project management and leadership
  • Stakeholder management and communication
  • Cost control and budgeting
  • Change and risk management
  • Document control and governance
  • Strategic scheduling and resource coordination

Education

  • Bachelor’s degree in science, engineering, or business (required)
  • Master’s degree in science, engineering, or business (preferred)

Additional Requirements

  • Ability to travel up to 10% of the time
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