Senior QA Professional
- Research & Development
- Denmark - Søborg
QA R&D within Quality R&D, Novo Nordisk A/S, Søborg, is seeking a QA Professional with drive and personality. Would you enjoy the high activity of the QA work within a broad spectrum of Novo Nordisk quality? Would you like to drive quality improvements where you represent QA as collaborator with stakeholders? Do you find motivation in an ever changing mix of routine tasks and non-routine tasks for you to organise and influence?
Then you might be the Senior QA Professional with the drive and performance we need.
About the department
QA R&D is responsible for driving consistency and compliance of Novo Nordisk Quality Management System (NN QMS) in Research & Development. The main responsibilities of the department are ISO9001 and QMS in general. The department consists of 18 employees split in three teams: the RA team, IT Quality Support team and the QMS team. The new position is placed in the RA team and the team will consist of five employees after this expansion. The RA team is focussing on NN QMS for the area Regulatory Affairs (RA) including a GMP regulated area. Team responsibilities include; secondary packaging material, review and approval of Standard Operating Procedures, handling Non-Conformities, support to stakeholders in Denmark as well as globally.
The job
As a QA Professional you will take an active role in the QA approval process in the global regulatory area. Our stakeholders’ primary regulatory requirements are GMP, ISO9001 and QMS and also include the print and packing material developing processes. You will interact with many other professionals and working cultures. Together with the QA RA-team and stakeholders you will get an opportunity to identify and define quality tasks and increase the quality mind set within Novo Nordisk. Quality improvement is one of our focus areas and QA must be an active participant in defining and executing future improvement activities/projects. The position is based in Søborg, Denmark.
Qualifications
You have a relevant scientific academic degree or equivalent and a strong command of written and spoken English. It is an advantage if you have been in a QA job before and have knowledge of the approval process of Non-Conformities, Change Requests, SOP reviews and the graphic processes. Qualifications within processes of labelling, packaging and cLEAN will also be regarded as a plus. Preferably, but not necessarily, you have significant project participation experience with cross functional projects. With your good cooperation and communication skills you are able to organise and drive tasks. Furthermore good presentation skills will be an advantage.
You take a pragmatic approach to problem solving and have strong interpersonal skills. You are detail-oriented with a strong quality mind set and are a team player, but also able to work independently. You thrive on working across departments in an international organisation.
We look for an open minded person with an outgoing attitude, natural networking skills. And we would enjoy having a straightforward person with a good sense of humour in our team and department.
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 Anders Ravn Sørensen at +45 3079 4724 or Lone Bau at +45 3075 7225.
Deadline
6 October 2013.
- Research & Development
- Denmark - Søborg
QA R&D within Quality R&D, Novo Nordisk A/S, Søborg, is seeking a QA Professional with drive and personality. Would you enjoy the high activity of the QA work within a broad spectrum of Novo Nordisk quality? Would you like to drive quality improvements where you represent QA as collaborator with stakeholders? Do you find motivation in an ever changing mix of routine tasks and non-routine tasks for you to organise and influence?
Then you might be the Senior QA Professional with the drive and performance we need.
About the department
QA R&D is responsible for driving consistency and compliance of Novo Nordisk Quality Management System (NN QMS) in Research & Development. The main responsibilities of the department are ISO9001 and QMS in general. The department consists of 18 employees split in three teams: the RA team, IT Quality Support team and the QMS team. The new position is placed in the RA team and the team will consist of five employees after this expansion. The RA team is focussing on NN QMS for the area Regulatory Affairs (RA) including a GMP regulated area. Team responsibilities include; secondary packaging material, review and approval of Standard Operating Procedures, handling Non-Conformities, support to stakeholders in Denmark as well as globally.
The job
As a QA Professional you will take an active role in the QA approval process in the global regulatory area. Our stakeholders’ primary regulatory requirements are GMP, ISO9001 and QMS and also include the print and packing material developing processes. You will interact with many other professionals and working cultures. Together with the QA RA-team and stakeholders you will get an opportunity to identify and define quality tasks and increase the quality mind set within Novo Nordisk. Quality improvement is one of our focus areas and QA must be an active participant in defining and executing future improvement activities/projects. The position is based in Søborg, Denmark.
Qualifications
You have a relevant scientific academic degree or equivalent and a strong command of written and spoken English. It is an advantage if you have been in a QA job before and have knowledge of the approval process of Non-Conformities, Change Requests, SOP reviews and the graphic processes. Qualifications within processes of labelling, packaging and cLEAN will also be regarded as a plus. Preferably, but not necessarily, you have significant project participation experience with cross functional projects. With your good cooperation and communication skills you are able to organise and drive tasks. Furthermore good presentation skills will be an advantage.
You take a pragmatic approach to problem solving and have strong interpersonal skills. You are detail-oriented with a strong quality mind set and are a team player, but also able to work independently. You thrive on working across departments in an international organisation.
We look for an open minded person with an outgoing attitude, natural networking skills. And we would enjoy having a straightforward person with a good sense of humour in our team and department.
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 Anders Ravn Sørensen at +45 3079 4724 or Lone Bau at +45 3075 7225.
Deadline
6 October 2013.