Novo Nordisk A/S
Ballerup, 1 stilling
- Research & Development
- Denmark - Måløv
Are you looking for new challenges within 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 pilot production of solid protein dosage forms towards clinical trials.
About the department
We are creating a new QC team of 12 employees in department of Oral Analytical Development and the department will be organised in three teams, Development, Support and QC. We will be 48 colleagues, who are responsible for development, validation of analytical methods and analytical support for oral protein products for preclinical and clinical trials. The department covers a broad range of analytical technologies.
The job
The QC team will carry out analytical support to phase 3 of oral formulations of proteins. The analytical methods cover chromatographic methods (HPLC/UPLC methods) and methods for solid dose formulation (e.g. dissolution). Other key tasks include analytical support to GMP stability, formulation and process development. The different tasks involve planning, troubleshooting, NC and OOS handling and evaluation of the analytical work in collaboration with laboratory technicians. You contribute actively to ensure documentation of analytical work to the right quality level and maintain the quality system in the team.
You can look forward to work with the challenges that arise when proteins/peptides are formulated as solid dosage forms. The position involves close collaboration with colleagues from formulation and process development.
Qualifications
You hold an MSc or PhD in Pharmacy or Engineering or a related field within analytical support for oral solid dosage forms. Ideally, you have a background in the pharmaceutical industry with QC experiences, and you use LEAN as a natural element in your leadership and find it interesting working according to GMP. Experience with analysis of tablet/capsules and/or proteins and chromatography 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 meet 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.
Application in Danish or English.
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 more information on the position, please contact Anders Bach Nielsen +45 3075 3889.
Deadline
30 October 2015.
