Jobbet "Senior Device Engineer for Device Manufacturing Development" er udløbet.
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  • Production Support
  • Denmark - Hillerød

Are you eager to deliver the best prefilled devices to the market? Do you enjoy close collaboration with stakeholders all over the world? Then, you may be our new device engineer in the prefilled device area of Device Manufacturing Development. The position is based in Hillerød, Denmark, and will support our sites around the world, ensuring that our product quality remains at the same high level, at all times as our production volume and number of products are growing.

About the department
In your new position, you will be a part of the Prefilled Product Maintenance team. You will join 12 highly skilled and motivated colleagues, who are responsible for Product Maintenance of the prefilled devices as well as Quality Specifications and methods. Wehave the overall responsibility for preparing standards, test setups and strategies for existing and future pre-filled devices. We drive numerous projects in the above areas, as well as within SOP compliance, standardisations, training and follow-up on quality activities.

The job
Together with your colleagues in the Prefilled Product Maintenance team, you will be responsible for developing, maintaining and optimising Quality Frame Specifications and their related test procedures for prefilled devices at our various production sites. The responsibility will also include establishing new methods and method verification, method transfer to sites, maintaining uncertainty budgets for the test methods, coordinating inter-calibration studies between the various laboratories, leading development projects within the Prefilled Devices area and following-up on deliverables to development projects.

Your challenge will be to function both as an expert within your field and also as a project leader. As many of the production sites and equipment suppliers are located outside Denmark, travel activities must be expected.

Qualifications
You have a background in mechanical or chemical engineering or similar, and are trained in relevant areas such as design control, metrology and measurement systems, validation and GMP. It would be an advantage if you have experience with measurement/test equipment for finished product devices and have worked with change requests in a GMP environment. You have a strong personal drive to achieve results, you work in a structured way, and you understand how to balance central and local initiatives in the project work.

As you will be interacting with many people inside and outside the organisation, strong communication skills and the ability to work with people at different levels are needed. Fluency in English, spoken and written, is required. Lastly, you have a global mind-set and are keen to operate in a changing and dynamic work environment.

We can offer you a world-class opportunity for professional growth together with inspiring and committed colleagues. At the same time, you will be part of a company that believes in making a difference – to patients, to the medical profession and to society.

Contact
For additional information, please contact Aurélie Søgaard-Christensen, +45 3075 7573 or Signe Munkholm Hoeck at +45 3079 7854.

Deadline
24 August 2014

Please write in your application that you've seen the job at Jobfinder