QA Professional
- Quality
- Denmark - Kalundborg
Would you like to join us in making a difference to people with haemophilia? 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®. 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.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.Your language skills cover proficiency in both Danish and English. Feel free to submit your job application in either English or Danish, whichever you prefer.
At Novo Nordisk we use our skills, dedication and ambition to help people with Haemophilia, and change their lives. By working with us you will have the opportunity to do the same in a global business environment.
Contact
For further information, please contact Yasar Salam Patruss on +45 30799247 or Susanne Kristensen on +45 3075 1113.Learn more about Novo Nordisk ProductSupply and working in QA using this link www.novonordisk.com/careers/QA.
Deadline
18 August 2013
- Quality
- Denmark - Kalundborg
Would you like to join us in making a difference to people with haemophilia? 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®. 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.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.Your language skills cover proficiency in both Danish and English. Feel free to submit your job application in either English or Danish, whichever you prefer.
At Novo Nordisk we use our skills, dedication and ambition to help people with Haemophilia, and change their lives. By working with us you will have the opportunity to do the same in a global business environment.
Contact
For further information, please contact Yasar Salam Patruss on +45 30799247 or Susanne Kristensen on +45 3075 1113.Learn more about Novo Nordisk ProductSupply and working in QA using this link www.novonordisk.com/careers/QA.
Deadline
18 August 2013