Key Leadership Role for Pharmaceutical Capacity Expansion

5 days ago


Køge, Køge Kommune, Denmark Novo Nordisk Full time

We are seeking a highly skilled Senior Project Manager to lead our Brown Field Investment Program in Köge, Denmark. This is an exciting opportunity to drive change and spearhead the establishment of manufacturing capacity for new products.

As a key member of our Project Management Office team, you will be responsible for leading one of our largest investment programs, ensuring production capacity for new products. This involves decommissioning an old facility and establishing a new production line from conceptual brief to validated process ready for manufacturing of pharmaceutical ingredients for our customers.

Your main responsibilities will include:

  • Leading a complex program of subprojects and interacting with a group of team members (internal and external), including Project Coordinators, Project Planner and Controllers, specialists, engineers, and operators.
  • Heading up a steering committee on behalf of the project/program owner, preparing progress reporting and conducting steering committee meetings.
  • Creating, together with key project members, a project plan with appropriate levels of detail and presenting these plans to senior management.
  • Utilizing the established governance within project management to provide clarity on responsibilities and expectations in your project team, meeting structure, feedback procedures, and the routines of collaboration.

This is a dynamic role that requires strong leadership skills, strategic thinking, and effective communication. You will work closely with highly skilled colleagues, collaborators, and external consultants in a combined effort to achieve project goals.

To succeed in this role, we imagine that you possess:

  • A Master's degree or Bachelor's degree within Engineering, Life Sciences, Project Management, or a related field.
  • Extensive experience in project management of capacity projects within the life science industry.
  • GMP qualification, validation, and/or automation experience, as well as a proven record of managing stakeholders at all levels.
  • Experience with decommissioning, new process lines, Active Pharmaceutical Ingredients (API), and carcinogenic substances.

The estimated salary for this role is around 100,000 - 120,000 EUR per annum, depending on experience. If you have a passion for leading complex projects and driving business growth, we encourage you to apply for this exciting opportunity.



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