Development Scientist in CMC Development. HOVEDSTADEN
Oferta de empleo de Ingenieros químicos en HOVEDSTADEN (Dinamarca)
Clasificación del trabajo:Profesionales científicos e intelectuales : Profesionales de las ciencias y de la ingeniería : Ingenieros (excluyendo electrotecnólogos) : Ingenieros químicos. Arbejde, der forudsætter viden på højeste niveau inden for pågældende område : Arbejde inden for naturvidenskab og ingeniørvirksomhed : Ingeniørarbejde (undtagen inden for elektroteknologi) : Ingeniørarbejde inden for kemi.
Descripción de la oferta de trabajo:
-?Research & Development -?Denmark - Bagsværd Having raw materials used for production to clinical trials in control is an increasing complex and challenging task. We are looking for a dedicated professional with ambition and drive to strengthen our GMP Raw Materials team. About the department As part of Novo Nordisk’s R&D family, CMC (Chemistry, Manufacturing and Control) Development makes a real difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for non-clinical and clinical trials which is a complicated journey that requires about 10 years of dedicated work in CMC Development. CMC Development is an ambitious organisation with a strong culture. We always seek to solve problems have an eye for the entire business and do our best to deliver despite any obstacles along the way. CMC API (Active Pharmaceutical Ingredient) Development is responsible for developing, upscaling and documenting fermentation, purification and chemical processes for API production in order to bring the growing pipeline of new drug candidates into clinical trials. The position As GMP Raw Material responsible you will join a multidisciplinary team with key responsibilities concerning raw materials used for clinical production. The main task is to manage and coordinate the introduction of new and existing raw materials into our growing development project portfolio. This is an important and complex process with numerous stakeholders where you are to ensure proper evaluation and documentation of the suitability of the materials for the intended use. You will be responsible for managing the complete raw material value chain from the manufacturer through development, sourcing and QA (Quality Assurance) professionals to the final use of the materials in our pilot facilities producing APIs for clinical trials. This includes working with ambitious timelines and quality requirements to ensure timely delivery. You will also be responsible for development and maintenance of documentation in consistency with authority and GMP guidelines to ensure sufficient control of the various materials. In addition, managing and facilitating smaller projects and continuously improving our working processes is a natural part of the job. Thus, you will contribute to interdisciplinary project teams and have the opportunity to develop both your project management and personal skills. Qualifications You hold a scientific academic degree in engineering, biology, chemistry or another relevant discipline at master level or above. You are enthusiastic, open-minded and a good communicator by nature. Moreover you are full of initiative and able to work both independently and in a team environment and you have a mind-set to continuously improve our working processes. Preferably you have experience with raw materials used for GMP production. Previous experience or relevant courses within project management will be an asset. Working at Novo Nordisk 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 Hans Kjær Poulsen at +45 3079 2250 or Sebastian Brandes at +45 3079 6178. Deadline 27 August 2017.
Servicio de empleo de origen:AMS, Servicios Públicos de Empleo, Dinamarca.