stillingsbetegnelse: QA Professional

jobbeskrivelse:
- Quality - Denmark - Hillerød Would you like to help securing Novo Nordisk A/S portfolio of devices continuously are improved to the benefit of our customers? Do you get energised by working in a team; handle multiple tasks on a daily basis in a global environment? Then you might be the person we are looking for in Device Manufacturing Development (DMD) QA. About the department Device Manufacturing Development (DMD) is dedicated to be the best manufacturing development partner in the field of medical devices. Our dedication, as a QA organisation, is to get superior quality built into our processes to ensure excellent quality of our finished devices. In DMD Product Maintenance QA we are responsible for securing the specified quality of our devices and combination products. The job You will contribute by ensuring the right product quality through activities related to Assembly and Pack QA. You will drive the quality assurance activities in relation to maintaining and creating the documentation of all our marketed devices and combination products. More concrete - you will drive the QA reviewer tasks on validation of new and old equipment as well as complex incident handling, change requests and non-conformities etc. You will be QA responsible for approving validation documentation for assembly and packaging production at a high level, ensuring that the specified level will ensure high quality products fulfilling all regulatory requirements. You will help ensuring that Quality has a high focus when new foot prints around the globe is created. In your daily work, you will interact with several departments internally, externally and abroad. Your success will depend on your ability to collaborate and communication with all types of colleagues and business partners while keeping the quality of the products in mind. The position offers you a unique opportunity to leave your mark while realising your goals and seeing the benefits of your work. Overall, you will have a great degree of freedom in the job, working where you can plan your own day-to-day work. Travel activities can occur. Qualifications You hold a relevant academic degree, maybe in engineering, pharmacy or equivalent. Optimally you have at least 3-5 years of experience. Preferable your academic background is topped with experience within quality assurance and/or device industry. You have an excellent quality mind-set, good communicational skills and you can place the importance of product quality, patient safety and compliance on the agenda in a positive and constructive way. Your language skills cover proficiency in English, and it is an advantage if you have knowledge with the requirements ISO 13485, 21 CFR Part 820 and 21 CFR Part 4. As a person, you are known for a high commitment as well as taking responsibility for your assignments. You work independently and make decisions regarding quality tasks and at the same time, you perform well in a team-oriented environment. At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development. Contact For further information, please contact Nick Thomsen at +45 3079 7859. Deadline 20 November 2015.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse: Farmaceutarbejde

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark