QA Chemist
- Quality
- Denmark - Gentofte
Would you like to help securing release of Novo Nordisk A/S haemophilia portfolio, growth hormone portfolio and Glucagon filled product? 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 two existing aseptic filling plants in Gentofte, the building of a new filling plant in Kalundborg and all utility systems in the Gentofte production areas. Our key tasks are to review and approve all sorts of GMP documentation such as validation reports, change requests, 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 45 highly skilled and competent colleagues working in four 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
We have two vacant position situated in two different releasing teams for the filling plants in Gentofte. Both jobs include QA review of several types of documents related to release of pharmaceutical products. The documents comes from all types of processes in a filling plant, such as formulation, wash and sterilisation processes, filling, freeze-drying, and visual inspection. One of the vacant positions includes evening work with QA presence in the production area approximately two-three times pr. month.
Your main responsibility will be to quality assure the filling plants 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 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 talented newly academic graduates.
You must thrive in a role where you are required to take leadership in order to achieve the shared targets in cooperation with your stakeholders. You have a strong quality mind-set, meet your deadlines, and know how to prioritise between different tasks in a dynamic environment. You are a dedicated team player who inspires trust amongst colleagues and partners. Your language skills cover proficiency in both Danish and English.
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.
Your application is welcome in Danish or English.
Contact
For further information, please contact QA Director Rikke Wissing Jensen at +45 3075 1566.
Deadline
2 January 2014
- Quality
- Denmark - Gentofte
Would you like to help securing release of Novo Nordisk A/S haemophilia portfolio, growth hormone portfolio and Glucagon filled product? 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 two existing aseptic filling plants in Gentofte, the building of a new filling plant in Kalundborg and all utility systems in the Gentofte production areas. Our key tasks are to review and approve all sorts of GMP documentation such as validation reports, change requests, 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 45 highly skilled and competent colleagues working in four 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
We have two vacant position situated in two different releasing teams for the filling plants in Gentofte. Both jobs include QA review of several types of documents related to release of pharmaceutical products. The documents comes from all types of processes in a filling plant, such as formulation, wash and sterilisation processes, filling, freeze-drying, and visual inspection. One of the vacant positions includes evening work with QA presence in the production area approximately two-three times pr. month.
Your main responsibility will be to quality assure the filling plants 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 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 talented newly academic graduates.
You must thrive in a role where you are required to take leadership in order to achieve the shared targets in cooperation with your stakeholders. You have a strong quality mind-set, meet your deadlines, and know how to prioritise between different tasks in a dynamic environment. You are a dedicated team player who inspires trust amongst colleagues and partners. Your language skills cover proficiency in both Danish and English.
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.
Your application is welcome in Danish or English.
Contact
For further information, please contact QA Director Rikke Wissing Jensen at +45 3075 1566.
Deadline
2 January 2014