QA Chemist
- Quality
- Denmark - Hillerød
Do you want to be part of Quality Assurance and ensure a high level of quality of Novo Nordisk’s insulin products and hereby make a difference for thousands of people? In QA Finished Products (FP) we are looking for a talented and ambitious QA chemist, with a desire to work in our FP production in Hillerød.
About the department
The new position is an expansion so that we are ready to ensure the quality level in 2014. You will join a dynamic department of 31 employees, divided into three teams; two in FP and one in the Aseptic Production (AP). You will join one of the FP teams, which consist of 8 highly skilled colleagues from different professional backgrounds.
You will become part of an ambitious team with an informal relation, good humour and where we take care of each other, and in that way you will rapidly, as a new employee, become a part of the team.
The Job
The team is responsible for assuring that systems and processes in relation to FlexPen® and the Quality Control (QC) area are in compliance with GMP requirements, and at the same time, act as compliance support to our production teams.
We work in a fast pace and our key tasks are review and approval of all types of GMP documentation; such as batch, change requests, non-conformities and validation reports all this with the common goal of releasing insulin products to our customers.
On top of that, QA is an important player at internal audits and external authority inspections, where you are expected to participate and present data when needed.
In this fast paced and dynamic environment, prioritisation can quickly change, whereby no days are the same and you will constantly be challenged, both in regards to the complexity of the tasks but also on tight deadlines.
Being a new member of the team, you will undergo a structured and individual training program with one of your colleagues acting as the trainer, and you can expect increasingly more responsibility. Subsequently, you will have an individual development plan to ensure continuous development and realization of your potential.
Qualifications
You hold an academic degree, e.g. pharmacist, veterinarian, biochemist, or similar. GMP experience or work experience from the pharmaceutical industry is preferred, but it is not a requirement.
Most importantly; you thrive in a fast-paced environment where you can take the lead and set directions in order to achieve business goals and at the same time you never compromise on quality, authority demands or deadlines. You are structured and a good coordinator and know how to prioritise between different quality tasks - All this with a positive mind-set.
Finally, you can communicate in both Danish and English written as well as spoken.
Feel free to submit your job application, as quickly as possible, in either English or Danish.
You can learn more about working as QA in Novo Nordisk by clicking on this link: www.novonordisk.com/careers/QA
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Heidi Bisgaard Jensen on phone + 45 3075 3147.
Deadline
17 December 2013
- Quality
- Denmark - Hillerød
Do you want to be part of Quality Assurance and ensure a high level of quality of Novo Nordisk’s insulin products and hereby make a difference for thousands of people? In QA Finished Products (FP) we are looking for a talented and ambitious QA chemist, with a desire to work in our FP production in Hillerød.
About the department
The new position is an expansion so that we are ready to ensure the quality level in 2014. You will join a dynamic department of 31 employees, divided into three teams; two in FP and one in the Aseptic Production (AP). You will join one of the FP teams, which consist of 8 highly skilled colleagues from different professional backgrounds.
You will become part of an ambitious team with an informal relation, good humour and where we take care of each other, and in that way you will rapidly, as a new employee, become a part of the team.
The Job
The team is responsible for assuring that systems and processes in relation to FlexPen® and the Quality Control (QC) area are in compliance with GMP requirements, and at the same time, act as compliance support to our production teams.
We work in a fast pace and our key tasks are review and approval of all types of GMP documentation; such as batch, change requests, non-conformities and validation reports all this with the common goal of releasing insulin products to our customers.
On top of that, QA is an important player at internal audits and external authority inspections, where you are expected to participate and present data when needed.
In this fast paced and dynamic environment, prioritisation can quickly change, whereby no days are the same and you will constantly be challenged, both in regards to the complexity of the tasks but also on tight deadlines.
Being a new member of the team, you will undergo a structured and individual training program with one of your colleagues acting as the trainer, and you can expect increasingly more responsibility. Subsequently, you will have an individual development plan to ensure continuous development and realization of your potential.
Qualifications
You hold an academic degree, e.g. pharmacist, veterinarian, biochemist, or similar. GMP experience or work experience from the pharmaceutical industry is preferred, but it is not a requirement.
Most importantly; you thrive in a fast-paced environment where you can take the lead and set directions in order to achieve business goals and at the same time you never compromise on quality, authority demands or deadlines. You are structured and a good coordinator and know how to prioritise between different quality tasks - All this with a positive mind-set.
Finally, you can communicate in both Danish and English written as well as spoken.
Feel free to submit your job application, as quickly as possible, in either English or Danish.
You can learn more about working as QA in Novo Nordisk by clicking on this link: www.novonordisk.com/careers/QA
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Heidi Bisgaard Jensen on phone + 45 3075 3147.
Deadline
17 December 2013