Senior R&D QA Professional with a strong drive
- Research & Development
- Denmark - Søborg
The RA Team within R&D QA, Novo Nordisk A/S, Søborg, is seeking a Senior QA Professional with drive and good co-operation skills. Would you enjoy the high activity of QA work within the broad spectrum of Novo Nordisk Quality Assurance? Would you like to drive quality improvements where you represent QA in collaboration 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
R&D QA 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 NN QMS in general. The department consists of 18 employees split into 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 Regulatory Affairs (RA) area 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 Senior 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 are looking for an open-minded person with an outgoing attitude and natural networking skills. And we would enjoy having a straightforward person with a good sense of humour in our team and department. Social competencies are important in this position both for us and our stakeholders.
Maybe you have other competencies in connection to quality and improvement projects from another background which you believe could be an advantage. If so please include these in your application, and tell us how you can add value to R&D Quality in Novo Nordisk.
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 +45 3075 7225.
Deadline
15. December 2013.
- Research & Development
- Denmark - Søborg
The RA Team within R&D QA, Novo Nordisk A/S, Søborg, is seeking a Senior QA Professional with drive and good co-operation skills. Would you enjoy the high activity of QA work within the broad spectrum of Novo Nordisk Quality Assurance? Would you like to drive quality improvements where you represent QA in collaboration 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
R&D QA 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 NN QMS in general. The department consists of 18 employees split into 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 Regulatory Affairs (RA) area 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 Senior 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 are looking for an open-minded person with an outgoing attitude and natural networking skills. And we would enjoy having a straightforward person with a good sense of humour in our team and department. Social competencies are important in this position both for us and our stakeholders.
Maybe you have other competencies in connection to quality and improvement projects from another background which you believe could be an advantage. If so please include these in your application, and tell us how you can add value to R&D Quality in Novo Nordisk.
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 +45 3075 7225.
Deadline
15. December 2013.