Process Supporter
- Production
- Denmark - Gentofte
Are you able to keep focus, prioritize and get to the root cause of problems in a hectic working environment? Are you motivated by keeping the production running? Do you take pride in ensuring documentation meet GMP standards? Then you could be the next colleague to strengthen our support team.
About the department
We are a small production facility located in Gentofte, responsible for the purification of Glucagon. Organised in Product Supply, Biopharm API, we are 30 colleagues who work closely together and take pride in having a challenging and fun working environment. In the Process & Support team we are 10 chemists, technicians and engineers who, together with the department’s two specialists, support the production team and ensure timely release of high quality Glucagon to current GMP standards.
The job
You will join our group of four chemists responsible for the production processes. Depending on your background and interests you will be the primary responsible for one of the purification steps, cleaning validations and/or environmental monitoring. You will be working closely with the 14 dedicated operators in the production team to ensure the production is carried out according to current standards. You will handle deviations in non-conformity reports, review documentation for release and write instructions. You will identify possible process optimizations in close corporation with the production team and lead the continuous improvements within your area. When our facility is being audited you will represent the department and confidently present relevant documentation. You will ensure to maintain the good relations with our stakeholders through your close collaboration with QA, Support and the laboratories.
Qualifications
You hold a degree as a pharmacist, chemical engineer or equivalent. You have a natural understanding of GMP as our license to operate. You have the ability to keep focus in a highly complex working environment. You use LEAN tools and systematic problem solving methods in order to find the root cause of problems and develop better standards in order to prevent them from reoccurring. You have a positive, will-do attitude and take responsibility to ensure deadlines are met. You start every day with enthusiasm and your great communication skills make it naturally for you to work closely with colleagues from different parts of the organisation. Besides being fluent in Danish you master English on a professional level.
If you want to become our new colleague, we will look forward to receiving you application in Danish or English, as you prefer.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development
Contact
For further information, please contcat Pernille Nyvang Jørgensen +45 3075 6948.
Deadline
8 December 2013
- Production
- Denmark - Gentofte
Are you able to keep focus, prioritize and get to the root cause of problems in a hectic working environment? Are you motivated by keeping the production running? Do you take pride in ensuring documentation meet GMP standards? Then you could be the next colleague to strengthen our support team.
About the department
We are a small production facility located in Gentofte, responsible for the purification of Glucagon. Organised in Product Supply, Biopharm API, we are 30 colleagues who work closely together and take pride in having a challenging and fun working environment. In the Process & Support team we are 10 chemists, technicians and engineers who, together with the department’s two specialists, support the production team and ensure timely release of high quality Glucagon to current GMP standards.
The job
You will join our group of four chemists responsible for the production processes. Depending on your background and interests you will be the primary responsible for one of the purification steps, cleaning validations and/or environmental monitoring. You will be working closely with the 14 dedicated operators in the production team to ensure the production is carried out according to current standards. You will handle deviations in non-conformity reports, review documentation for release and write instructions. You will identify possible process optimizations in close corporation with the production team and lead the continuous improvements within your area. When our facility is being audited you will represent the department and confidently present relevant documentation. You will ensure to maintain the good relations with our stakeholders through your close collaboration with QA, Support and the laboratories.
Qualifications
You hold a degree as a pharmacist, chemical engineer or equivalent. You have a natural understanding of GMP as our license to operate. You have the ability to keep focus in a highly complex working environment. You use LEAN tools and systematic problem solving methods in order to find the root cause of problems and develop better standards in order to prevent them from reoccurring. You have a positive, will-do attitude and take responsibility to ensure deadlines are met. You start every day with enthusiasm and your great communication skills make it naturally for you to work closely with colleagues from different parts of the organisation. Besides being fluent in Danish you master English on a professional level.
If you want to become our new colleague, we will look forward to receiving you application in Danish or English, as you prefer.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development
Contact
For further information, please contcat Pernille Nyvang Jørgensen +45 3075 6948.
Deadline
8 December 2013