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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