Medicon Village

Senior Project Manager Rebranding

On behalf one of our vey exciting customers within the pharmaceutical industry, we are now looking for a skilled project manager with a solid track record from the pharmaceutical or medical device industry who is willing to immediately take on a crucial roll in the rebranding process that the company is currently carrying out.

In this specific project you will be working cross functionally within IT, Regulatory and Commercial and report directly to the Global Director PMO. This assignment may also be the start of a permanent engagement in the organisation where you as a senior project manager will work in close contact with customers (internal and external) in complex projects within development and manufacturing of pharmaceuticals and drug-device combination products and production care. The projects include all phases of pharmaceutical development projects and production care projects. Internal investment projects are within the scope of this position. Part of the role includes project data analysis, adaptations and maintenance of the company´s project management tool.

 

Your responsibilities

  • Deliver within the constraints of the project in terms of time, budget and scope
  • Develop financially justified business cases, reflecting the project value for the client and for the company
  • Coordinate work efforts, keep up the pace and provide clarity through active day-to-day management
  • Update and maintain our project management system with project details, schedules, resources, financials, project logs and overall status
  • Take responsibility for ensuring that relevant project documentation is stored
  • Maintain project financials (in terms of cost, revenue and budget)
  • Plan and control all work included in the project
  • Visualize the project´s content and results
  • Agree on resources and manage the project team
  • Manage project uncertainty through active risk management
  • Lead (or participate in) developing project quotations
  • Contribute to improving ways of working, systems, processes and training
  • Data analysis and project management tool maintenance

Your qualifications and experience

  • Academic degree or comparable. Background in pharmaceutical, chemical, biological or related field. Minimum 10 years of experience working in a regulated environment (healthcare, pharma or medical devices)
  • Good understanding of GMP procedures and the way of working in the pharmaceutical industry
  • Extensive experience in managing multiple complex projects, programs, and/or portfolios in parallel
  • Experience in building long-term partnerships with clients, based on a combination of technology platforms
  • Experience working in multi-disciplinary teams, including pharmaceutical development, pharmaceutical engineering, analytical development, clinical supplies, regulatory and other CMC related roles
  • Solid financial education or equivalent experience in managing budgets, costs and profitability
  • Preferably certifications in project management techniques and methodologies (e.g. PMI, IPMA e t c) and comfortable in working with agile project management
  • Experience in working with advanced project management and business intelligence tools and systems.

We expect a high level of commitment and that you have the ability to motivate and inspire others to perform of the highest standards. You have an approachable and collaborative attitude with a natural ability to work cross functional and form solid business relationships. You are structured, self-motivated, and result-driven with a high degree of integrity and ownership.

AND - you can contribute to a fun and enjoyable work environment!

If you feel that you are a match we ask you to apply asap. Since the assignment is urgent you should be able to start more or less immediately . The employment will initially be temporary. We will review applications on an ongoing basis. You are of course very welcome to contact us for any questions regarding the position and the assignment. Welcome!