QA Chemist
- Quality
- Denmark - Gentofte
Would you like to help securing release of Novo Nordisk A/S Glucagon? Do you thrive when working in a team; handling multiple tasks of high complexity? Then you might be the person we are looking for in Biopharm QA Aseptic Production.
About the department
Biopharm QA AP is responsible for quality assurance of three existing aseptic filling plants and the building of a new filling plant, two laboratories and all utility systems in the Gen-tofte production areas. Our key tasks are to review and approve all sorts of GMP docu-mentation such as validation reports, change requests and
non-conformities and batch documentation in order to be able to release filled product for packaging.
As QA Chemist in Biopharm QA AP you will join a group of highly skilled and competent colleagues working in five teams lead by separate associate managers. By joining us you will get the chance of professional and personal development and you will get an excellent and unique overview of current authority expectations and demands in the pharmaceutical industry.
The Job
The vacant position is situated in Gentofte in one of our releasing teams for filling plants. The team consists of 4 chemists. The job includes QA review of several types of docu-ments hereunder release of Glucagon. The documents come from all types of processes thus ensuring a high level of variety on a daily business.
Your main responsibility will be to quality assure the release of Glucagon. And thereby contribute to assure product quality and compliance with the current GMP rules and guidelines. On top of that QA is a major player at internal audits and external authority inspections, where you are expected to participate.
When started you will undergo an individual and intense training program, where you can expect to be given more responsibility gradually.
Qualifications
You hold an academic degree that qualify you as QP (Qualified Person) according to the Danish Medical Agency. Preferable your academic background is topped with experience either from the pharmaceutical industry. However we would also like to hear from talent-ed newly academic graduates.
It is important that you thrive in a role where you are required to take independent deci-sions and show a high degree of authority. You have a strong quality mind-set and you are robust. You know and meet your deadlines and you are capable of prioritising between different tasks in a dynamic environment. You are a dedicated team player who inspires trust and respect amongst colleagues and partners. Your language skills cover proficiency in both Danish and English.
Your application is welcome in Danish or English.
In Novo Nordisk is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information, please contact Tejs Skarregaard Pedersen at +45 3075 5361 or Rikke Wissing Jensen at +45 3075 1566.
Deadline
29 July 2013.
- Quality
- Denmark - Gentofte
Would you like to help securing release of Novo Nordisk A/S Glucagon? Do you thrive when working in a team; handling multiple tasks of high complexity? Then you might be the person we are looking for in Biopharm QA Aseptic Production.
About the department
Biopharm QA AP is responsible for quality assurance of three existing aseptic filling plants and the building of a new filling plant, two laboratories and all utility systems in the Gen-tofte production areas. Our key tasks are to review and approve all sorts of GMP docu-mentation such as validation reports, change requests and
non-conformities and batch documentation in order to be able to release filled product for packaging.
As QA Chemist in Biopharm QA AP you will join a group of highly skilled and competent colleagues working in five teams lead by separate associate managers. By joining us you will get the chance of professional and personal development and you will get an excellent and unique overview of current authority expectations and demands in the pharmaceutical industry.
The Job
The vacant position is situated in Gentofte in one of our releasing teams for filling plants. The team consists of 4 chemists. The job includes QA review of several types of docu-ments hereunder release of Glucagon. The documents come from all types of processes thus ensuring a high level of variety on a daily business.
Your main responsibility will be to quality assure the release of Glucagon. And thereby contribute to assure product quality and compliance with the current GMP rules and guidelines. On top of that QA is a major player at internal audits and external authority inspections, where you are expected to participate.
When started you will undergo an individual and intense training program, where you can expect to be given more responsibility gradually.
Qualifications
You hold an academic degree that qualify you as QP (Qualified Person) according to the Danish Medical Agency. Preferable your academic background is topped with experience either from the pharmaceutical industry. However we would also like to hear from talent-ed newly academic graduates.
It is important that you thrive in a role where you are required to take independent deci-sions and show a high degree of authority. You have a strong quality mind-set and you are robust. You know and meet your deadlines and you are capable of prioritising between different tasks in a dynamic environment. You are a dedicated team player who inspires trust and respect amongst colleagues and partners. Your language skills cover proficiency in both Danish and English.
Your application is welcome in Danish or English.
In Novo Nordisk is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information, please contact Tejs Skarregaard Pedersen at +45 3075 5361 or Rikke Wissing Jensen at +45 3075 1566.
Deadline
29 July 2013.