Cultivation Specialist
- Production
- Denmark - Gentofte
Are you interested in working with our broad portfolio of products in Biopharm and help us in being Fast to market? In Biopharm Manufacturing Development we are responsible for support to our productions, transfer of new products from R&D and continuous optimizations of our many processes.
About the department
In Biopharm Manufacturing Development, Active Pharmaceutical Ingredients Support we are looking for a Cultivation Specialist willing to undertake the overall cultivation responsibility for production of haemophilia products and growth hormones. Look forward to varying working days in your new department, which constitutes an important link between Novo Nordisk R&D and production. You will be situated in Gentofte, Denmark.
The job
Help set direction and solve scientifically challenging cases. Your main objectives will be to manage the cross organisational process group for cultivation with focus on scientifically challenging cases and knowledge sharing across the organisation. You will be a key stakeholder in developing, implementing and supporting the cultivation strategies for products from late development to production. You will also be involved in cross organisational optimisations and systematic problem solving. You will join the management group of Biopharm API Support but also be involved in cultivation activities across Novo Nordisk globally. You will be helping with prioritisation of incoming assignments and setting strategic direction. You can anticipate a wide cooperation with e.g. the production, Quality Assurance, R&D, Regulatory Affairs, analytical departments and project groups.
This job is an opportunity to blend the urge to dive deep into cultivation on the one hand and influence the managerial decision-making on the other hand.
Qualifications
M.Sc with vast experience from a pharmaceutical production or R&D function. You hold an MSc in e.g. Civil Engineering, Biology, or Biotechnology with solid insight into upstream development in biomanufacturing. Your CV mirrors more than 7 years of experience from a pharmaceutical production or R&D function within the protein area. In addition, you have insight into GMP and are familiar with the current industry standards for process validation and regulatory standards for documentation. You have a systematic and structured approach to working with data and sound communication skills in Danish and English, enabling you to document your work meticulously. Besides, you can effortlessly cooperate with colleagues from various backgrounds, and you thrive on leading the way and training your colleagues. You are capable of sharing knowledge at any organisational level, and with your extrovert and proactive attitude you can easily establish a network across the organisation. Finally, you have a keen eye for quality and manage to prioritise your work to meet every deadline.
At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change possibilities in haemophilia. By working with us you will have the opportunity to do the same in a global business environment.
Contact
For further information, please contact Casper Leuenhagen at +45 3079 4751.
Deadline
31 August 2013.
- Production
- Denmark - Gentofte
Are you interested in working with our broad portfolio of products in Biopharm and help us in being Fast to market? In Biopharm Manufacturing Development we are responsible for support to our productions, transfer of new products from R&D and continuous optimizations of our many processes.
About the department
In Biopharm Manufacturing Development, Active Pharmaceutical Ingredients Support we are looking for a Cultivation Specialist willing to undertake the overall cultivation responsibility for production of haemophilia products and growth hormones. Look forward to varying working days in your new department, which constitutes an important link between Novo Nordisk R&D and production. You will be situated in Gentofte, Denmark.
The job
Help set direction and solve scientifically challenging cases. Your main objectives will be to manage the cross organisational process group for cultivation with focus on scientifically challenging cases and knowledge sharing across the organisation. You will be a key stakeholder in developing, implementing and supporting the cultivation strategies for products from late development to production. You will also be involved in cross organisational optimisations and systematic problem solving. You will join the management group of Biopharm API Support but also be involved in cultivation activities across Novo Nordisk globally. You will be helping with prioritisation of incoming assignments and setting strategic direction. You can anticipate a wide cooperation with e.g. the production, Quality Assurance, R&D, Regulatory Affairs, analytical departments and project groups.
This job is an opportunity to blend the urge to dive deep into cultivation on the one hand and influence the managerial decision-making on the other hand.
Qualifications
M.Sc with vast experience from a pharmaceutical production or R&D function. You hold an MSc in e.g. Civil Engineering, Biology, or Biotechnology with solid insight into upstream development in biomanufacturing. Your CV mirrors more than 7 years of experience from a pharmaceutical production or R&D function within the protein area. In addition, you have insight into GMP and are familiar with the current industry standards for process validation and regulatory standards for documentation. You have a systematic and structured approach to working with data and sound communication skills in Danish and English, enabling you to document your work meticulously. Besides, you can effortlessly cooperate with colleagues from various backgrounds, and you thrive on leading the way and training your colleagues. You are capable of sharing knowledge at any organisational level, and with your extrovert and proactive attitude you can easily establish a network across the organisation. Finally, you have a keen eye for quality and manage to prioritise your work to meet every deadline.
At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change possibilities in haemophilia. By working with us you will have the opportunity to do the same in a global business environment.
Contact
For further information, please contact Casper Leuenhagen at +45 3079 4751.
Deadline
31 August 2013.