Validation Support Engineer in Device R&D

Validation Support Engineer in Device R&D

• Validation
• Denmark - Hillerød

Do you want to take your validation skills to the next level? Are you motivated by being part of an innovative and research focused organisation? Do you have interest in IT systems? Can you deliver top class quality in every aspect of your work in an efficient way? If you can answer yes to these questions, we might have the right job opportunity for you!

Device Research and Development (R&D) has a long and outstanding track record of developing the best, most innovative and widely used injection devices in the world. In the development of medical devices, we ensure that user insight and innovation go hand in hand with a strong quality mind-set.

About the department
You will join our team IT Tools & Validation, which is a part of the System Engineering Support department in device R&D. IT Tools & Validation is responsible for specifying, developing, purchasing, and validating new test equipment to support verification of medical devices, thus playing an important role in the device development process. We collaborate with stakeholders across the organisation striving for excellence in everything we do.

The position
Your main task will be validation and qualification of test equipment, participate in test and measurement processes and develop testing competences to improve device development. You will write, correct and review the work instruction and also take ownership in change requests. You will be responsible for equipment maintenance.

You will establish good test equipment set up aligning with Quality Assurance (QA). You will provide support to teams using test equipment across Device R&D Department.

You will be responsible for validation of equipment developed internally or externally according to predefined requirements. You will support all aspects of validation activities. You will evaluate equipment and processes, analyse collected data against pre-determined criteria, and prepare final reports in compliance with regulations, industrial practices, and Novo Nordisk policies and procedures.

The department is evolving within the field, which means that you will be expected to participate in the on-going efforts to further develop our methodology within maintenance, test procedures, training, and validation of equipment.

Qualifications
Qualified candidates will at least hold a BSc in a Science, IT, Technical or Engineering related field. You have at least two years of experience in validation and/or as a Test Engineer with equipment responsibility in larger companies in the regulated industry. You must have strong written and verbal communication skills in English and solid analytical skills. Experience in qualification and validation of test equipment (within computer, mechanical or similar systems) is a must, as would experience in the execution of protocols. You are having good stakeholder management both internally and externally. You will provide insight to testing equipment.

Your ability to structure, plan and manage your work will be a key factor to your success. You must be able to work independently and excel in a dynamic, hands-on department where things move at a fast pace and changes come rapidly.

Working at Novo Nordisk
At Novo Nordisk it is your skills, your commitment and your ambitions that help us improve the lives of many people. In return, we offer you the opportunity to work with highly committed colleagues.

Contact
For further information, please contact Lisbeth Sivertsen at +45 3075 1840.

Deadline 
2 July 2017.

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