stillingsbetegnelse:
Senior Process Scientist – break new land within Solid Dosage Forms

jobbeskrivelse:
- Research & Development - Denmark - Måløv Our growth is your opportunity Being part of Novo Nordisk Research & Development means working at one of the world's largest and most successful biopharmaceutical companies. Our R&D organisation is vital to Novo Nordisk's continued growth and we always welcome talented people who would like to grow with us. Novo Nordisk has set out on a voyage towards the development and production of oral formulations of proteins. Our ambition is to develop breakthrough products based on orally available versions of insulin and GLP-1. As Senior Process Scientist you will be a key player bringing your skills and enthusiasm into formulation and process development of solid dosage forms. About the department 36 scientists and technicians are organised in two teams. We are overall responsible for development of solid dosage form of Insulin and GLP-1 molecules for oral delivery. The formulation development covers from early phase development of oral protein formulations and processes in small scale to later stages of formulation development in larger scale. In the later phase the progress towards robust manufacturing processes is of critical importance. We use rational design, statistical and QbD principles in our formulation and process development. The job You will play an absolute key role in our business critical efforts to ensure process expertise and input to a new pilot plant. Your main task will be to connect our solid dosage form process development with selection and documentation of the right equipment and supplier. This includes ensuring that requirements are appropriately defined and established. Another vital task will be to contribute with process expertise in the formulation of rationales and scientific content for the equipment qualification documents. In this you will work in close collaboration with our highly qualified validation responsible. You will provide input for process qualification as planning and definition of the test strategy, definition of requirements, and selection of methods of analyses, acceptance criteria, formulas, support test and review of results. In addition, you will handle, review and approve of validation documentation and specific validation plans. Finally, you will represent the department in multidisciplinary project groups, in which you work closely with Formulation Scientists, Pilot Production Scientists, Consultants, Qualification and Validation Experts. Qualifications You have a Master’s Degree in Pharmacy, Engineering, Chemistry or a related field. This is backed by at least 5 years’ experience from a pharmaceutical company where you have worked intensively with process optimisation of pharmaceutical products. Preferably, you have experience with equipment for solid dosage forms e.g. within mixing, granulation, compression, coating or pharmaceutical-technical analyses. If not, you value these areas of expertise as the natural next step for your development. You are used to taking full responsibility for your assignments, and you are known for your proactive work approach and high commitment to find constructive solutions to complex challenges. With your open and positive attitude you enjoy working in a dynamic environment where teamwork is at the top of the agenda. At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment. Contact For further information please call Lone Løgstrup Kimer on +45 3079 3569. Deadline 9 February 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