Support Chemist
- Production
- Denmark - Hillerød
Would you like to work with new products and help people with Haemophilia to live their lives the way they want? We offer you a dynamic job in close interaction with talented and dedicated colleagues. Your contribution will be significant in preparing the facility for market production and FDA inspection.
About the department
Biopharm API Mammalian Cell Production II is placed in Hillerød, consists of ~60 employees and is currently producing Haemophilia products for clinical trials phase III. We are running several parallel projects to increase production capacity and to prepare the process and facility for market production. The production process consists of cultivation of mammalian cells and a recovery process based on liquid chromatography.
The Job
As a support chemist you will facilitate a smooth running production with timely release of batches. You will spend time on the shop-floor, knowing that being close to the process and the operators will help you solving problems early and effectively. You never compromise on quality, since being in compliance with SOP’s and cGMP is our license to operate. Depending on your skills and experience you will be involved in one or more of the parallel projects running in the department: The capacity expansion building project, qualification of equipment, optimization of CIP and SIP processes, cleaning validation and preparing for process validation. Successful passage of FDA inspection will be an important milestone for you and the rest of the department.
Qualifications
You are a M.Sc. or have a similar scientific education. You have a strong mindset for quality and compliance and preferable LEAN experience. As a person you can stay focused in a sometimes busy working day and you always approach tasks and colleagues with a positive attitude and energy. You are analytical and work in a structural way and are used to deliver according to deadlines. The ideal candidate has previously worked with mammalian cell culture, chromatography in large scale and has experience with starting up new facilities including qualification and validation. You possess good communication skills both in Danish and English. The ideal candidate has previously worked with Cleaning Validation and knowledge to drive a large validation project in a new organisation.
In Biopharm API Mammalian Cell Production II we use our skills, dedication and ambition to continuously improve our processes. By working with us you will have the opportunity to do the same and can look forward to a dynamic and varied working day with an informal atmosphere and good colleagues.
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, Kell Øberg at +45 3079 1570 or Kenneth Petersen at +45 3075 6156.
Deadline
8 January 2014.
- Production
- Denmark - Hillerød
Would you like to work with new products and help people with Haemophilia to live their lives the way they want? We offer you a dynamic job in close interaction with talented and dedicated colleagues. Your contribution will be significant in preparing the facility for market production and FDA inspection.
About the department
Biopharm API Mammalian Cell Production II is placed in Hillerød, consists of ~60 employees and is currently producing Haemophilia products for clinical trials phase III. We are running several parallel projects to increase production capacity and to prepare the process and facility for market production. The production process consists of cultivation of mammalian cells and a recovery process based on liquid chromatography.
The Job
As a support chemist you will facilitate a smooth running production with timely release of batches. You will spend time on the shop-floor, knowing that being close to the process and the operators will help you solving problems early and effectively. You never compromise on quality, since being in compliance with SOP’s and cGMP is our license to operate. Depending on your skills and experience you will be involved in one or more of the parallel projects running in the department: The capacity expansion building project, qualification of equipment, optimization of CIP and SIP processes, cleaning validation and preparing for process validation. Successful passage of FDA inspection will be an important milestone for you and the rest of the department.
Qualifications
You are a M.Sc. or have a similar scientific education. You have a strong mindset for quality and compliance and preferable LEAN experience. As a person you can stay focused in a sometimes busy working day and you always approach tasks and colleagues with a positive attitude and energy. You are analytical and work in a structural way and are used to deliver according to deadlines. The ideal candidate has previously worked with mammalian cell culture, chromatography in large scale and has experience with starting up new facilities including qualification and validation. You possess good communication skills both in Danish and English. The ideal candidate has previously worked with Cleaning Validation and knowledge to drive a large validation project in a new organisation.
In Biopharm API Mammalian Cell Production II we use our skills, dedication and ambition to continuously improve our processes. By working with us you will have the opportunity to do the same and can look forward to a dynamic and varied working day with an informal atmosphere and good colleagues.
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, Kell Øberg at +45 3079 1570 or Kenneth Petersen at +45 3075 6156.
Deadline
8 January 2014.