Kemiker
- Quality
- Denmark - Måløv
Are you committed to support a GMP production in Novo Nordisk? Right now, we are looking for an analytical chemist with a high quality to Quality Control laboratory of Biopharm Tablets & Finished Products.
About the department
The QC department (414) is made up of about 60 dedicated employees divided into three teams. We are responsible for quality control and analysis of existing and new Novo Nordisk HRT and OAD tablet products, and we work with HPLC analysis, microbiology, dissolution and pharmaceutical technical analysis. We are also responsible for stability and complaints analyses as well as climate room facilities. We are looking for a new colleague to join Team Mix, a group that primarily performs analysis of Vagifem/VLD.
The job
You will be responsible for analytical methods; primarily pharmaceutical technical analysis and you must have an interest in analytical equipment and IT. You will help to ensure that the methods are in accordance with current regulatory requirements, including preparation of protocols, reports, analysis specifications and registration documents. In addition to this, daily tasks will include, for example, approval of analysis results and participation in problem solving with regard to these as well as in relation to transfer and validation studies. At the same time, you will use your knowledge to support and advise both your assistant chemist colleagues and our collaborative partners. You will also help to continuously improve the quality of our work as you engage in tasks/projects across the department. You can look forward to building many contacts both within this department and other departments and laboratories at Novo Nordisk.
Qualifications
We imagine you have a solid theoretical background, an academic degree (Cand. Pharm, chemical engineer or the equivalent) and experience with HPLC, laboratory IT systems and pharmaceutical technical analysis from previous employment or university studies. You also have experience with statistics and general chemical analytical methods, as well as validation of these. You need a good understanding of GMP requirements and preferably you have knowledge of the LEAN principles.
As you will be in daily contact with a broad range of people with different backgrounds, it is a requirement that you are good at communicating in both Danish and English, using written and spoken language. In addition, it is of course important that you work in a structured manner and understand how to follow up and complete tasks yourself, while at the same time contributing to helping the department achieve its goals. As a person you are motivated, full of initiative, solution oriented and someone who likes working in a team where the key attributes are cooperation, tolerance and a good sense of humour.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Kenneth Lokind on +45 3075 6083.
Deadline
6 September 2013.
- Quality
- Denmark - Måløv
Are you committed to support a GMP production in Novo Nordisk? Right now, we are looking for an analytical chemist with a high quality to Quality Control laboratory of Biopharm Tablets & Finished Products.
About the department
The QC department (414) is made up of about 60 dedicated employees divided into three teams. We are responsible for quality control and analysis of existing and new Novo Nordisk HRT and OAD tablet products, and we work with HPLC analysis, microbiology, dissolution and pharmaceutical technical analysis. We are also responsible for stability and complaints analyses as well as climate room facilities. We are looking for a new colleague to join Team Mix, a group that primarily performs analysis of Vagifem/VLD.
The job
You will be responsible for analytical methods; primarily pharmaceutical technical analysis and you must have an interest in analytical equipment and IT. You will help to ensure that the methods are in accordance with current regulatory requirements, including preparation of protocols, reports, analysis specifications and registration documents. In addition to this, daily tasks will include, for example, approval of analysis results and participation in problem solving with regard to these as well as in relation to transfer and validation studies. At the same time, you will use your knowledge to support and advise both your assistant chemist colleagues and our collaborative partners. You will also help to continuously improve the quality of our work as you engage in tasks/projects across the department. You can look forward to building many contacts both within this department and other departments and laboratories at Novo Nordisk.
Qualifications
We imagine you have a solid theoretical background, an academic degree (Cand. Pharm, chemical engineer or the equivalent) and experience with HPLC, laboratory IT systems and pharmaceutical technical analysis from previous employment or university studies. You also have experience with statistics and general chemical analytical methods, as well as validation of these. You need a good understanding of GMP requirements and preferably you have knowledge of the LEAN principles.
As you will be in daily contact with a broad range of people with different backgrounds, it is a requirement that you are good at communicating in both Danish and English, using written and spoken language. In addition, it is of course important that you work in a structured manner and understand how to follow up and complete tasks yourself, while at the same time contributing to helping the department achieve its goals. As a person you are motivated, full of initiative, solution oriented and someone who likes working in a team where the key attributes are cooperation, tolerance and a good sense of humour.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Kenneth Lokind on +45 3075 6083.
Deadline
6 September 2013.