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Project Manager/Analysis Coordinator to Analytical Support

Are you looking for new challenges? Would you like to plan and manage late clinical phase project activities and improve the analytical methods and processes for Novo Nordisk's new diabetes products? Would you like to support the world's largest insulin production site? Then you may be the energetic, competent and independent Project Manager we need in the analytical support lab.

About the department
The department is responsible for the late phase development and validation of “new product” analytical methods, prior to transfer to Quality Control (QC) departments. The department also provides analysis support to optimisation projects in Novo Nordisk's Diabetes Active Pharmaceutical Ingredient (DAPI) production. Lastly the department plays a crucial role in supporting the production and the quality control laboratories. We are 65 committed employees divided into four teams. You will coordinate your projects across the entire department.

The position
You will work as a Project Manager/Analysis Coordinator (AC) for one or more of the department's development projects in close contact with our senior project managers, the chemists and laboratory staff and the leadership team in the department.

As a Project Manager/AC, you are responsible for coordinating the transfer of the analysis package from R&D, to Manufacturing Development (MDev) and further on to the QC laboratories which support marketed products. During this period you will coordinate analysis of large-scale production for phase 3 studies as well as plan and manage activities related to robustness tests and validation across the four teams in the department.

In this job you will be in close contact with a large part of Novo Nordisk's diabetes business and work with many different stake holders; including Chemistry, Manufacturing and Control (CMC) Supply, who is responsible for the early development of clinical trials, Regulatory Affairs, Quality Assurance, Production and Quality Control laboratories. As a Project Manager, you ensure that your project deliveries comply with applicable standards including GMP, and that the mature methods are suitable for Quality Control. Flexibility and problem solving become a natural part of everyday life.

Qualifications
You must have a relevant natural science education, (Chemical Engineer, Pharmacist, Cand. Scient., etc.), and thereby have a good theoretical and practical understanding of protein chemistry and chromatographic techniques such as HPLC / UPLC. The ideal candidate also has theoretical and practical experience with ELISA, Western Blot, Southern Blot, cell-based assays and MS techniques, as well as Good Manufacturing Processes, but it is not a requirement. It is also a great advantage if you have experience with optimisation, validation and transfer of analytical methods.

We expect you to be committed and show a high level of independence. We also expect that you are good at creating a clear overview and prioritising your tasks; even when the deadline is approaching. You never compromise on quality and are also good at completing your tasks on time, then moving on to the next task with enthusiasm and energy. You have good communication skills and are good at working with all types of professional groups.

All in all, we offer a very exciting job, in the intersection between Research & Development and production with good development opportunities for the right candidate.

Working at Novo Nordisk
Novo Nordisk in Kalundborg is the world's largest insulin production site big enough to have a 5.5 km run around the site and to produce half of the insulin used worldwide. This is a workplace for more than 2,800 dedicated Novo Nordisk employees who set ambitious goals and strive to make a difference for our more than 24 million patients through stable deliveries of high quality products.

The site is in rapid development with lots of exciting challenges. We solve them by being at the forefront of technology, systems, methods and processes, and by assembling teams of talented employees.

In Novo Nordisk it is your ability, your commitment and your ambitions which help us improve the lives of many people. On the other hand, we offer you the opportunity to work with talented colleagues and we offer you a wide range of opportunities for professional and personal development.

Contact
Do you have any questions regarding the position or want to know more? Feel free to contact Ida Brunn Steinmüller on+45 3079 2253 or Thomas Lundberg Rand on +45 3075 8448.

Deadline
24 July 2018.


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329831994Phoenix-8c23f7f212018-06-14T00:00:00Project Manager/Analysis Coordinator to Analytical Support

Are you looking for new challenges? Would you like to plan and manage late clinical phase project activities and improve the analytical methods and processes for Novo Nordisk's new diabetes products? Would you like to support the world's largest insulin production site? Then you may be the energetic, competent and independent Project Manager we need in the analytical support lab.

About the department
The department is responsible for the late phase development and validation of “new product” analytical methods, prior to transfer to Quality Control (QC) departments. The department also provides analysis support to optimisation projects in Novo Nordisk's Diabetes Active Pharmaceutical Ingredient (DAPI) production. Lastly the department plays a crucial role in supporting the production and the quality control laboratories. We are 65 committed employees divided into four teams. You will coordinate your projects across the entire department.

The position
You will work as a Project Manager/Analysis Coordinator (AC) for one or more of the department's development projects in close contact with our senior project managers, the chemists and laboratory staff and the leadership team in the department.

As a Project Manager/AC, you are responsible for coordinating the transfer of the analysis package from R&D, to Manufacturing Development (MDev) and further on to the QC laboratories which support marketed products. During this period you will coordinate analysis of large-scale production for phase 3 studies as well as plan and manage activities related to robustness tests and validation across the four teams in the department.

In this job you will be in close contact with a large part of Novo Nordisk's diabetes business and work with many different stake holders; including Chemistry, Manufacturing and Control (CMC) Supply, who is responsible for the early development of clinical trials, Regulatory Affairs, Quality Assurance, Production and Quality Control laboratories. As a Project Manager, you ensure that your project deliveries comply with applicable standards including GMP, and that the mature methods are suitable for Quality Control. Flexibility and problem solving become a natural part of everyday life.

Qualifications
You must have a relevant natural science education, (Chemical Engineer, Pharmacist, Cand. Scient., etc.), and thereby have a good theoretical and practical understanding of protein chemistry and chromatographic techniques such as HPLC / UPLC. The ideal candidate also has theoretical and practical experience with ELISA, Western Blot, Southern Blot, cell-based assays and MS techniques, as well as Good Manufacturing Processes, but it is not a requirement. It is also a great advantage if you have experience with optimisation, validation and transfer of analytical methods.

We expect you to be committed and show a high level of independence. We also expect that you are good at creating a clear overview and prioritising your tasks; even when the deadline is approaching. You never compromise on quality and are also good at completing your tasks on time, then moving on to the next task with enthusiasm and energy. You have good communication skills and are good at working with all types of professional groups.

All in all, we offer a very exciting job, in the intersection between Research & Development and production with good development opportunities for the right candidate.

Working at Novo Nordisk
Novo Nordisk in Kalundborg is the world's largest insulin production site big enough to have a 5.5 km run around the site and to produce half of the insulin used worldwide. This is a workplace for more than 2,800 dedicated Novo Nordisk employees who set ambitious goals and strive to make a difference for our more than 24 million patients through stable deliveries of high quality products.

The site is in rapid development with lots of exciting challenges. We solve them by being at the forefront of technology, systems, methods and processes, and by assembling teams of talented employees.

In Novo Nordisk it is your ability, your commitment and your ambitions which help us improve the lives of many people. On the other hand, we offer you the opportunity to work with talented colleagues and we offer you a wide range of opportunities for professional and personal development.

Contact
Do you have any questions regarding the position or want to know more? Feel free to contact Ida Brunn Steinmüller on+45 3079 2253 or Thomas Lundberg Rand on +45 3075 8448.

Deadline
24 July 2018.

2018-07-25T00:50:20.433 Are you looking for new challenges? Would you like to plan and manage late clinical phase project activities and improve the analytical methods and processes for Novo Nordisk s new diabetes products? Would you like to support the world s largest insulin production site? Then you may be the energetic, competent and independent Project Manager we need in the analytical support lab. About the department The department is responsible for the late phase development and validation of new product analytical methods, prior to transfer to Quality Control (QC) departments. The department also provides analysis support to optimisation projects in Novo Nordisk s Diabetes Active Pharmaceutical Ingredient (DAPI) production. Lastly the department plays a crucial role in supporting the production and the quality control laboratories. We are 65 committed employees divided into four teams. You will coordinate your projects across the entire department. The position You will work as a Project Manager Analysis Coordinator (AC) for one or more of the department s development projects in close contact with our senior project managers, the chemists and laboratory staff and the leadership team in the department. As a Project Manager AC, you are responsible for coordinating the transfer of the analysis package from R D, to Manufacturing Development (MDev) and further on to the QC laboratories which support marketed products. During this period you will coordinate analysis of large-scale production for phase 3 studies as well as plan and manage activities related to robustness tests and validation across the four teams in the department. In this job you will be in close contact with a large part of Novo Nordisk s diabetes business and work with many different stake holders including Chemistry, Manufacturing and Control (CMC) Supply, who is responsible for the early development of clinical trials, Regulatory Affairs, Quality Assurance, Production and Quality Control laboratories. As a Project Manager, you ensure that your project deliveries comply with applicable standards including GMP, and that the mature methods are suitable for Quality Control. Flexibility and problem solving become a natural part of everyday life. Qualifications You must have a relevant natural science education, (Chemical Engineer, Pharmacist, Cand. Scient., etc.), and thereby have a good theoretical and practical understanding of protein chemistry and chromatographic techniques such as HPLC UPLC. The ideal candidate also has theoretical and practical experience with ELISA, Western Blot, Southern Blot, cell-based assays and MS techniques, as well as Good Manufacturing Processes, but it is not a requirement. It is also a great advantage if you have experience with optimisation, validation and transfer of analytical methods. We expect you to be committed and show a high level of independence. We also expect that you are good at creating a clear overview and prioritising your tasks even when the deadline is approaching. You never compromise on quality and are also good at completing your tasks on time, then moving on to the next task with enthusiasm and energy. You have good communication skills and are good at working with all types of professional groups. All in all, we offer a very exciting job, in the intersection between Research Development and production with good development opportunities for the right candidate. Working at Novo Nordisk Novo Nordisk in Kalundborg is the world s largest insulin production site big enough to have a 5.5 km run around the site and to produce half of the insulin used worldwide. This is a workplace for more than 2,800 dedicated Novo Nordisk employees who set ambitious goals and strive to make a difference for our more than 24 million patients through stable deliveries of high quality products. The site is in rapid development with lots of exciting challenges. We solve them by being at the forefront of technology, systems, methods and processes, and by assembling teams of talented employees. In Novo Nordisk it is your ability, your commitment and your ambitions which help us improve the lives of many people. On the other hand, we offer you the opportunity to work with talented colleagues and we offer you a wide range of opportunities for professional and personal development. Contact Do you have any questions regarding the position or want to know more? Feel free to contact Ida Brunn Steinmüller on 45 3079 2253 or Thomas Lundberg Rand on 45 3075 8448. Deadline 24 July 2018.11Jobnet8c23f7f2100000000000IDK_OFIR_02DKDanmark228DKK2018-07-24T00:00:000000https://www.novonordisk.com/careers/working-at-novo-nordisk/job-ad-display.56786BR.English.html0EuropaDanmarkSjælland & øerVestsjællandKalundborg3286230Novo Nordisk A/S11Hallas Alle 14400KalundborgDKDanmark155.6734547011.13269480
DKDanmarkDKDanmark
8Fuldtid46Permanent590263JobNet48404581000https://dispatcher.ofir.dk/statistic/register?context=FeedEntrySearchedCount&feedId=dc2beb84&entryId=8c23f7f2https://dispatcher.ofir.dk/statistic/register?context=FeedEntryDisplayCount&feedId=dc2beb84&entryId=8c23f7f2https://dispatcher.ofir.dk/statistic/register?context=JobApplicationInitiatedCount&feedId=dc2beb84&entryId=8c23f7f2&page=ShowJob&component=SendApplicationButtonhttps://dispatcher.ofir.dk/statistic/register?context=JobApplicationAppliedCount&feedId=dc2beb84&entryId=8c23f7f2&page=EmailApplyForm&component=SendApplicationButtonhttps://static.matchwork.com/company/logo/DK/ORS/SoMe/Ledelse_og_HR/Ledelse/2.jpgEr du en dygtig leder? Som Projektleder bliver du jævnligt mødt af spændende ledelsesrelaterede opgaver.12008001Dansk3Læse/ tale213111Projektleder6Ledelse355629428Ida Brunnnoreply@ofir.comDKDanmarkDKDanmarkda-DK