Specialist
- Production
- Denmark - Bagsværd
Do you want to develop your skills while securing world class aseptic production in a global environment?
About the department
Aseptic Production Support and Optimisation is a part of DFP Manufacturing Development. Our main focus is setting standards, providing process and technical support to Novo Nordisk’s insulin production sites globally. A vital part of this work is to implement technology strategies in Diabetes Finished Products (DFP). You will be a part of the Aseptic Production support team where 17 very experienced Specialists, Senior Project Managers, Professionals and Technicians are looking forward to your arrival.
The job
You will be the DFP specialist providing support and solutions within the Aseptic area to our production sites. You will be the strong backbone of aseptic production in Novo Nordisk, setting direction and providing guidance on all aspects of environmental monitoring, aseptic handling and keeping Novo Nordisk A/S best in class in your field of expertise.Your overall objective is to ensure compliance with regulatory requirements and authority expectations (GMP). At the same time you will provide handson investigations and support to the production teams. When performing support you identify areas with potential for optimisations, and at the same time you contribute to best practise sharing across the production sites and teams. Naturally, you will also bring your expertise into play when implementing new equipment or establishing new production facilities in order to ensure effective ramp up of sites. You will collaborate with process responsible and subject matter experts in our global DFP process groups. As many of the production sites and equipment suppliers are located abroad you can look forward to approximately 30 travel days per year.
Qualifications
You have a relevant academic degree as Microbiologist, Engineer, Pharmacist or similar backed by a minimum of 8 years’ practical experience from aseptic production of injectables. In addition, you have significant experience with pharmaceutical processes and equipment, and you have worked with aseptic processes in a GMP production environment. You therefore understand the regulatory environment, and ensuring compliance is a part of the way you work.Your structured way of working and general overview enables you to handle several tasks at a time and still keep an ongoing drive for results. Being open minded and positive you are a natural relation builder with people across organisational levels, geography and culture. To succeed it is also crucial that you thrive on working independently as well as part of a team. Finally, you are very good at English, written and spoken.
At Novo Nordisk, you will help some 366 million people who are living with diabetes. We expect high performance and the ambition to make your mark on our business. In exchange, we offer global opportunities for professional and personal development.
Contact
For further information, please call Steffen Elholm Andersen at +45 3079 4709.
Deadline
18 August 2013.
- Production
- Denmark - Bagsværd
Do you want to develop your skills while securing world class aseptic production in a global environment?
About the department
Aseptic Production Support and Optimisation is a part of DFP Manufacturing Development. Our main focus is setting standards, providing process and technical support to Novo Nordisk’s insulin production sites globally. A vital part of this work is to implement technology strategies in Diabetes Finished Products (DFP). You will be a part of the Aseptic Production support team where 17 very experienced Specialists, Senior Project Managers, Professionals and Technicians are looking forward to your arrival.
The job
You will be the DFP specialist providing support and solutions within the Aseptic area to our production sites. You will be the strong backbone of aseptic production in Novo Nordisk, setting direction and providing guidance on all aspects of environmental monitoring, aseptic handling and keeping Novo Nordisk A/S best in class in your field of expertise.Your overall objective is to ensure compliance with regulatory requirements and authority expectations (GMP). At the same time you will provide handson investigations and support to the production teams. When performing support you identify areas with potential for optimisations, and at the same time you contribute to best practise sharing across the production sites and teams. Naturally, you will also bring your expertise into play when implementing new equipment or establishing new production facilities in order to ensure effective ramp up of sites. You will collaborate with process responsible and subject matter experts in our global DFP process groups. As many of the production sites and equipment suppliers are located abroad you can look forward to approximately 30 travel days per year.
Qualifications
You have a relevant academic degree as Microbiologist, Engineer, Pharmacist or similar backed by a minimum of 8 years’ practical experience from aseptic production of injectables. In addition, you have significant experience with pharmaceutical processes and equipment, and you have worked with aseptic processes in a GMP production environment. You therefore understand the regulatory environment, and ensuring compliance is a part of the way you work.Your structured way of working and general overview enables you to handle several tasks at a time and still keep an ongoing drive for results. Being open minded and positive you are a natural relation builder with people across organisational levels, geography and culture. To succeed it is also crucial that you thrive on working independently as well as part of a team. Finally, you are very good at English, written and spoken.
At Novo Nordisk, you will help some 366 million people who are living with diabetes. We expect high performance and the ambition to make your mark on our business. In exchange, we offer global opportunities for professional and personal development.
Contact
For further information, please call Steffen Elholm Andersen at +45 3079 4709.
Deadline
18 August 2013.