Project Manager - New Product Coordinator
- Production
- Denmark - Gentofte
Do you thrive in a fast paced environment, juggling many challenges at the same time? Do you have a can-do attitude? Do you like to structure tasks having a flair for logistics? And do you enjoy interacting with a diverse set of stakeholders? If you can answer yes to these questions, you may be the New Product Coordinator we are looking for in Biopharm QC New Haemophilia.
About the department
Novo Nordisk, Biopharm QC New Haemophilia is a newly established laboratory with high quality and LEAN standards. We are responsible for chemical and biological analyses on finished products and API of Novo Nordisk new haemophilia products not yet on the market. In addition we have one marketed Haemophilia product. Because of this wide range of products, Biopharm QC New Haemophilia interacts with many internal stakeholders every day. Stakeholders are from both R&D, CMC and production. This requires a single point of contact for both our customers, but also for the organisation in Biopharm QC New Haemophilia. We offer a very exciting job with development opportunities among high competent colleagues in a positive working environment.
The job
As New Product Coordinator you communicate openly and honestly securing the interests of both Biopharm QC New Haemophilia and our stakeholders. You will be the link between Biopharm QC New Haemophilia and the rest of of Biopharm, through recurrent stakeholder meetings and management of our Service Level Agreements with these stakeholders. You will be involved in follow-up activities to ensure Biopharm QC New Haemophilia delivers as agreed. This is a position in which you will work closely together with the departments' local logistic planners and you will also enjoy a high degree of influence on the flow of incoming samples and their deadlines in Biopharm QC New Haemophilia. The responsibility for maintaining forecasts for sample flow related to existing and new facilities/products in Biopharm QC New Haemophilia will also be yours.
Additionally, you will be responsible for the departments' project/investment portfolio and act as a project manager on selected projects. Support to the performance boards, including update of KPIs will also be part of the job description. Project portfolio includes both internal improvement projects and cross-organisational projects.
You will work with all parts of the Biopharm QC organisation, and broadly with Biopharm CMC Production sites, providing you with the opportunity to thoroughly getting to know the supply chain with Biopharm. The position will provide you with indirect management experiences, and hence could be a stepping stone towards a leader position in Novo Nordisk.
Qualifications
You hold an MSC in pharmacy, biology, engineering or similar, supplemented with a minimum of 3 years' experience as a project manager. You are confident working in a GMP regulated environment. It will be an advantage if you have experience with laboratory or logistics.
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 call Lissi Falch on +45 3075 1015.
Deadline
20 December 2013.
- Production
- Denmark - Gentofte
Do you thrive in a fast paced environment, juggling many challenges at the same time? Do you have a can-do attitude? Do you like to structure tasks having a flair for logistics? And do you enjoy interacting with a diverse set of stakeholders? If you can answer yes to these questions, you may be the New Product Coordinator we are looking for in Biopharm QC New Haemophilia.
About the department
Novo Nordisk, Biopharm QC New Haemophilia is a newly established laboratory with high quality and LEAN standards. We are responsible for chemical and biological analyses on finished products and API of Novo Nordisk new haemophilia products not yet on the market. In addition we have one marketed Haemophilia product. Because of this wide range of products, Biopharm QC New Haemophilia interacts with many internal stakeholders every day. Stakeholders are from both R&D, CMC and production. This requires a single point of contact for both our customers, but also for the organisation in Biopharm QC New Haemophilia. We offer a very exciting job with development opportunities among high competent colleagues in a positive working environment.
The job
As New Product Coordinator you communicate openly and honestly securing the interests of both Biopharm QC New Haemophilia and our stakeholders. You will be the link between Biopharm QC New Haemophilia and the rest of of Biopharm, through recurrent stakeholder meetings and management of our Service Level Agreements with these stakeholders. You will be involved in follow-up activities to ensure Biopharm QC New Haemophilia delivers as agreed. This is a position in which you will work closely together with the departments' local logistic planners and you will also enjoy a high degree of influence on the flow of incoming samples and their deadlines in Biopharm QC New Haemophilia. The responsibility for maintaining forecasts for sample flow related to existing and new facilities/products in Biopharm QC New Haemophilia will also be yours.
Additionally, you will be responsible for the departments' project/investment portfolio and act as a project manager on selected projects. Support to the performance boards, including update of KPIs will also be part of the job description. Project portfolio includes both internal improvement projects and cross-organisational projects.
You will work with all parts of the Biopharm QC organisation, and broadly with Biopharm CMC Production sites, providing you with the opportunity to thoroughly getting to know the supply chain with Biopharm. The position will provide you with indirect management experiences, and hence could be a stepping stone towards a leader position in Novo Nordisk.
Qualifications
You hold an MSC in pharmacy, biology, engineering or similar, supplemented with a minimum of 3 years' experience as a project manager. You are confident working in a GMP regulated environment. It will be an advantage if you have experience with laboratory or logistics.
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 call Lissi Falch on +45 3075 1015.
Deadline
20 December 2013.