Expert within QA Quality Management System processes and projects
Ofertas de Farmacéuticos en HOVEDSTADEN (Dinamarca)
Clasificación del trabajo:Profesionales científicos e intelectuales : Profesionales de la salud : Otros profesionales de la salud : Farmacéuticos. Arbejde, der forudsætter viden på højeste niveau inden for pågældende område : Arbejde inden for sundhedsområdet : Andet sundhedsarbejde : Farmaceutarbejde.
Descripción de la oferta de trabajo:
-?Quality -?Denmark - Hillerød Would you like to be the Subject Matter Expert for Quality processes and participate/drive projects within Quality Assurance (QA) of Medical Devices and Combination Products? And are you highly motivated by working with stakeholder management across the organisation? Then you might be the person we are looking for in Device Manufacturing Development (DMD) QA. About the department You will be part of a team of 10 dedicated colleagues in Hillerød. Together, we are responsible for assuring the quality of manufacturing processes, laboratories and Quality Control for Novo Nordisk newest developed Medical Devices and Combination Products for pilot production and low volume production for clinical trials and launch to the market. We also have the responsibility of the Quality Management System and Quality processes in DMD. The team values professional sparring and you can look forward to entering into an energetic and positive working environment where cooperation is a keyword. Novo Nordisk is one of the world's most successful pharmaceuticals companies and has a strong growth potential. Part of this growth is due to the new products within the device portfolio being produced in DMD facilities. The position In this role, you will be the Subject Matter Expert for the processes Corrective Actions and Preventive Actions (CAPA) and Nonconformity (NC) Handling as well as responsible for driving and participate in quality projects across the organisation. You will be the key person for the DMD organisation setting the right standards for the processes CAPA and Nonconformity Handling in order to ensure robust and efficient production processes for high quality devices. A part of your job will also be to coordinate and provide successful training and support to DMD NC experts so they are able to support and teach end users timely and efficiently. Furthermore, you will ensure that we, in all aspects, are in compliance with both internal and external requirements. Qualifications You hold an academic degree preferably as Engineer, Pharmacist or similar. Furthermore, you have a minimum of 5 year work experience from the medical device or pharmaceutical business industry within Quality Assurance. You are outgoing, service-minded and have a strong quality mind-set and experience driving or as part of projects and process improvement. You should be comfortable with IT including proficiency use of the Microsoft package and have a high level of fluency in written and spoken English. On a personal level, you are known for dedicating yourself to work proactively to solve the task at hand. Using your ability to think out of the box, you are still able to come up with solutions and suggestions that comply with quality requirements. You are a team player and a skilled communicator and you thrive on unfolding your high level of energy and spirit in an international and dynamic environment. Feel free to submit your job application in either English or Danish, whichever you prefer. Working at Novo Nordisk At Novo Nordisk it is your skills, your commitment and your ambition, which help us to improve many people's lives. In return, we offer you the opportunity to work with exceptionally talented colleagues and a wide range of opportunities for professional and personal development. Contact For further information, please contact Dean Kloe at +45 3075 8948. Deadline 6 August 2017. Applications are reviewed on an ongoing basis, so please apply as soon as possible.
Servicio de empleo de origen:AMS, Servicios Públicos de Empleo, Dinamarca.