Site Master Plan Manager

Category:  Project Management & Agile
Location: 

Anagni, Lazio, IT

    

Are you ready to take on a pivotal role in shaping the future of our Anagni FFEx site? Do you have a knack for strategic planning and project management? If so, we invite you to join us as our new Site Master Plan Manager. Read more and apply today for a life-changing career.

 

End of 2024, Novo Nordisk acquired the manufacturing site Catalent Anagni S.r.l. with the ambition to expand our capacity to meet the needs of millions of patients. You will be part of a global team that will develop the pharma facilities of the future and work with advanced technology to rethink our fill & finish facilities.

 

The Position

The Site Master Plan Manager (SMPM) in the Anagni FFEx is overall responsible for driving, managing and updating the Site Master Plan (for what is included in the FFEx scope).The SMPM is the key driver of an “holistic view” on the whole Anagni FFEx Project taking care not only what is part of the AP, FP, IL and WH but also to all is an interlink and to what is an enabler. (AP is an Aseptic Production Module; FP is a Finished Product Module; IL is the Intra Logistic; WH is the Warehouse).

The SMPM is also a key interface for the Anagni Site to develop a complete Site Master Plan that must include not only what is related to the current on-going operations and to the current site CAPEX but also what must be put in place to integrate the future deliverables of the Anagni FFEx project.

 

Among your main responsibilities will be to:

 

  • Develop and maintain the site master plan: Create and update comprehensive plans for site development and infrastructure improvements and align the master plan with strategic business objectives and future growth projections.
  • Coordinate engineering projects and initiatives: Oversee the planning, execution, and completion of engineering projects and ensure projects are delivered on time, within budget, and meet quality standards.
  • Ensure compliance with safety and quality standards: Implement and monitor adherence to safety protocols and quality regulations and conduct regular audits and assessments to ensure compliance with industry standards.
  • Collaborate with cross-functional teams: Work closely with departments such as production, maintenance, and R&D to support engineering needs and facilitate communication and collaboration to achieve common goals.
  • Optimise resource allocation and utilisation: Analyse resource needs and allocate them efficiently across projects and identify opportunities to improve resource utilisation and reduce waste.

 

 

Qualifications

 

  • B. Sc. or M. Sc. in Engineering or similar.
  • At least 5 years of experience in defining, implementing and executing projects within the pharma industry.
  • Excellent insight into engineering supplier project role.
  • Excellent within project coordination and managing multi-disciplinary project groups.
  • Experience from operating in a GMP-regulated environment, and from qualification and validation of equipment/processes.
  • Strong flair for leadership, high degree of independence and a high degree of interaction. Moreover, it requires a high degree of authority and decision making to ensure progress and a sound knowledge of when issues and deviations need to be pro-actively elevated within project management.  Excellent team working skills are also a must.
  • Project Management training/certification, example IPMA Level A or Program Management Professional (PMI) is considered a plus.
  • High level of English.

 

 

About the Department

You will be part of the FFEx AN Engineering & Construction Management department based in Anagni, Italy. Our project is part of a global initiative with sister projects in Denmark, France, and the USA. You will be working on-site in Anagni, interacting with international engineering partners and collaborating across world time zones. The atmosphere is dynamic and collaborative, with a strong focus on innovation and excellence.

 

Working at Novo Nordisk

We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.

 

 

Contact

For further information and to apply directly please visit www.novonordisk.com/careers.

 

Deadline

Apply before March, 17th 2025.

 

 

 

    

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 

 

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.