Jobbet "Senior Project Manger for New Product Entry" er udløbet.
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Senior Project Manger for New Product Entry

  • Project Management
  • Denmark - Hillerød

In this job, millions of people worldwide depend on you to bringing the newest medical devices to market. Are you ready for playing a key role in driving a project for introducing new devices? Are you keen on ensuring the right and timely coordination between the Research & Development department and the relevant process experts, specialists and technicians in the production sites? Then you may be our new Senior Project Manager in the Prefilled department in Devices Manufacturing Development (DMD).

About the department
The job is located in Hillerød in Device Manufacturing Development (DMD). Our challenge is to execute an increasing portfolio of diverse development projects and bring them fast to market. You will join a dynamic department consisting of 35 dedicated and ambitious employees with various backgrounds striving for excellence within pharmaceutical finish production.

The job
You will be personally responsible for driving new projects from R&D to production, where the goal is to develop early phase pilot equipment towards high speed and high capacity production lines. In the project you will be responsible for securing and driving effective use of time and resources. In particular, you will be provide clear goals and purpose for the project and the project team members and inspire and motivate your team to deliver excellent results. You will identify and plan the various project activities in relation to bringing a new drug into Finished production e.g. Plans, Change Request cases, approvals, tests etc. You will also ensure coordination and progress through effective and transparent processes. You should expect approx. 10 travel days per year.

Qualifications
You have an MSc in Mechanical Engineering or similar, supplemented with a minimum of 2 years’ experience as a project manager within Finished pharmaceutical products or similar fiels such as knowledge management and/or quality and process support. Ideally, you have insight into device development and know what it means to operate in a GMP-regulated environment. On a personal level, you are a self-starter who thrives with driving tasks independently to the finish line. As you have a structured approach to your work, you can juggle several processes while prioritising your efforts optimally. You have a global mind-set and enjoy building relations across organisational levels and geography. Impeccable communication skills are a must as well as well as the ability to deliver high quality presentation material. Lastly, you must be fluent in both written and spoken English.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please contact Anders Nørbygaard +45 3075 2444.

Deadline
4 January 2015.

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