QA Professional
- Quality
- Denmark - Kalundborg
Would you like to join us in making a difference to people with hemophilia? And in realizing our ambition to help people with hemophilia live the lives they want?
About the department
A job is waiting for you in a challenging and developing environment. In Biopharm QA for FVII API in Kalundborg you will join a team with 11 engaged employees. Together we assure quality and compliance in the production of NovoSeven® and in the QC laboratory. The working relations are informal and the team value professional sparring and good humour highly.
The Job
You are responsible, together with competent and experienced colleagues, for the release of API, including among other tasks review of batch documentations, approval of non-conformities, instructions, validations and change requests. Your main responsibility area is purification of FVII API.
One of your primary objects is to perform review and approval in due time and in full compliance with the GMP standards. You assure quality products come up to the requirements of the authorities. Good relations and communication skills are key tools to handling the quality issues in the best possible way, and therefore you will proactively establish relations to your colleagues in the production.
Quality is the key word in this job and ensure quality and compliance, improve our operations and avoid errors are natural for you. As QA Professional, you are aware, purposeful and have impact, which means that you can stand firm if considerations of patient safety and company policy require it. Look forward to an exciting job where you have a high degree of responsibility. Naturally, we will provide you with relevant training.
Qualifications
You are a qualified pharmacist, engineer or have a Master of Science degree. Preferable your academic background is topped with experience from pharmaceutical industry. You are familiar with GMP and authority requirements for the pharmaceutical industry.
You work systematically and can take a comprehensive view and you are not afraid of taking decisions and get the job done. You are the kind of person who can work on their own. Moreover, you are purposeful and able to prioritise several tasks in a changing environment. You are good at building relations to colleagues and stakeholders across the organisation.
Precise communication is absolutely essential and you must be capable of taking part in various tasks and have the kind of impact that means you can stand firm in favour of compliance, product quality and patient safety.
In Novo Nordisk is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information, please contact Susanne Kristensen on +45 3075 1113 or Ulla Falkenberg on +45 3075 8890.
Deadline
16 June 2013.
- Quality
- Denmark - Kalundborg
Would you like to join us in making a difference to people with hemophilia? And in realizing our ambition to help people with hemophilia live the lives they want?
About the department
A job is waiting for you in a challenging and developing environment. In Biopharm QA for FVII API in Kalundborg you will join a team with 11 engaged employees. Together we assure quality and compliance in the production of NovoSeven® and in the QC laboratory. The working relations are informal and the team value professional sparring and good humour highly.
The Job
You are responsible, together with competent and experienced colleagues, for the release of API, including among other tasks review of batch documentations, approval of non-conformities, instructions, validations and change requests. Your main responsibility area is purification of FVII API.
One of your primary objects is to perform review and approval in due time and in full compliance with the GMP standards. You assure quality products come up to the requirements of the authorities. Good relations and communication skills are key tools to handling the quality issues in the best possible way, and therefore you will proactively establish relations to your colleagues in the production.
Quality is the key word in this job and ensure quality and compliance, improve our operations and avoid errors are natural for you. As QA Professional, you are aware, purposeful and have impact, which means that you can stand firm if considerations of patient safety and company policy require it. Look forward to an exciting job where you have a high degree of responsibility. Naturally, we will provide you with relevant training.
Qualifications
You are a qualified pharmacist, engineer or have a Master of Science degree. Preferable your academic background is topped with experience from pharmaceutical industry. You are familiar with GMP and authority requirements for the pharmaceutical industry.
You work systematically and can take a comprehensive view and you are not afraid of taking decisions and get the job done. You are the kind of person who can work on their own. Moreover, you are purposeful and able to prioritise several tasks in a changing environment. You are good at building relations to colleagues and stakeholders across the organisation.
Precise communication is absolutely essential and you must be capable of taking part in various tasks and have the kind of impact that means you can stand firm in favour of compliance, product quality and patient safety.
In Novo Nordisk is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information, please contact Susanne Kristensen on +45 3075 1113 or Ulla Falkenberg on +45 3075 8890.
Deadline
16 June 2013.