stillingsbetegnelse: Analytical Scientist

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. Are you looking for new challenges within formulation, process or analytical method development of solid dosage forms and do you want to make a difference? Our Oral Protein Formulation Unit (OPF) in Måløv is expanding therefore we are looking for several dedicated, professional and enthusiastic new colleagues. Novo Nordisk is on a voyage towards the development and production of oral formulations of proteins. Our ambition is to develop break-through products based on orally available versions of insulin and GLP-1. You will be involved in CMC activities for formulation/process development, pilot production, scale-up and analysis of solid protein dosage forms towards clinical trials. About the department We are 41 colleagues, who are organized in two teams. The department is responsible for stability studies and responsible for development of analytical methods and analytical support for oral protein products for preclinical and clinical trials. The department covers a broad range of analytical technologies (e.g. U/HPLC and dissolution). The job You will be responsible for stability in the department. Central tasks will be writing stability protocols and reports and stability trending of results from analytical methods for phase 1, 2 and 3. Other key tasks include providing analytical support to formulation and process development. The different tasks involve evaluation and reporting of analytical result and troubleshooting in collaboration with laboratory technicians and stakeholders. You contribute actively to ensure documentation of development stability studies to the right quality level and maintain the quality system in the team. You can look forward to working with the challenges that arise when proteins/peptides are formulated as solid dosage forms. The position involves close collaboration with colleagues from analytical development and formulation development. Qualifications You hold an MSc or PhD in Pharmacy or Engineering or a related field and have a minimum of 3-5 years of experience within stability monitoring for oral solid dosage forms or protein/peptides in the pharmaceutical industry. You have previously worked according to GMP and you are familiar with the principles of LEAN. Experience with analysis of tablet/capsules and/or proteins would be an advantage. On a personal level, you enjoy working with people from different professional backgrounds and in a team setup. You are dedicated to meeting the team goals and contributing to a good team spirit and with your systematic approach, you are able to overview many tasks at the same time and work independently. 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 more information on the position, please contact Thomas Falck +45 3075 7650. Deadline 11 March 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