Temp QA for QC
- Quality
- Denmark - Gentofte
Would you like to be part of Quality Assurance in Biopharm QA for QC?
Biopharm QA AP is looking for a talented and ambitious QA Chemist for a one year temporary position for Quality Assurance of the Quality Control laboratories situated in Gentofte and Kalundborg. In this job you will be offered exciting opportunities to increase your experience within quality assurance.
About the department
Biopharm QA AP is responsible for Quality Assurance of three existing aseptic filling plants and the building of a new one, three laboratories 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 and non-conformities 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.
The job
The vacant position is situated in the team responsible for assuring the microbiological and the chemical control laboratories. The team consists of 7 chemists. The job includes QA review of several types of documents related to chemical and microbiological analysis. The position is situated in Gentofte but you have to support the laboratory in Kalundborg and meet in Kalunborg 1-2 times a week.Your main responsibility will be to quality assure the laboratories and thereby contribute to assure, that the products always are of high quality and analysed in full compliance with the current 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 from the pharmaceutical industry. However we would also like to hear from talented newly academic graduates.It is important that you thrive in a role where you are required to take independent decisions and show a high degree of authority. You have a strong quality mindset 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.
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 associate manager Ulla Thinggaard at +45 30752104 or Department manager Rikke Wissing Jensen at +45 3075 1566.
Deadline
1 August 2013.
- Quality
- Denmark - Gentofte
Would you like to be part of Quality Assurance in Biopharm QA for QC?
Biopharm QA AP is looking for a talented and ambitious QA Chemist for a one year temporary position for Quality Assurance of the Quality Control laboratories situated in Gentofte and Kalundborg. In this job you will be offered exciting opportunities to increase your experience within quality assurance.
About the department
Biopharm QA AP is responsible for Quality Assurance of three existing aseptic filling plants and the building of a new one, three laboratories 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 and non-conformities 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.
The job
The vacant position is situated in the team responsible for assuring the microbiological and the chemical control laboratories. The team consists of 7 chemists. The job includes QA review of several types of documents related to chemical and microbiological analysis. The position is situated in Gentofte but you have to support the laboratory in Kalundborg and meet in Kalunborg 1-2 times a week.Your main responsibility will be to quality assure the laboratories and thereby contribute to assure, that the products always are of high quality and analysed in full compliance with the current 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 from the pharmaceutical industry. However we would also like to hear from talented newly academic graduates.It is important that you thrive in a role where you are required to take independent decisions and show a high degree of authority. You have a strong quality mindset 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.
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 associate manager Ulla Thinggaard at +45 30752104 or Department manager Rikke Wissing Jensen at +45 3075 1566.
Deadline
1 August 2013.