Job opportunity:
QA Professional – for 18 Months temporary vacancy
- Quality
- Denmark - Gentofte
Would you like to join us in making a difference to people with growth hormone deficiency? Would you like to be responsible for quality assurance of qualification and validation tasks? If the answer is yes, Biopharm QA API Gentofte is looking for a talented and ambitious QA Professional for a temporary position.
About the department
Biopharm QA API is a dynamic department with 35 people, divided into 3 teams who are responsible for the quality assurance of API for marketed pharmaceutical products.
We are currently expanding our department and have an open positions in our Facility team. You will become part of a well-functioning, self-steering team with 7 dedicated colleagues. You will be responsible for the technical part of quality assurance. The working relations are informal and helpful and the team values professional sparring and good humour highly.
The Job
As a QA professional you will be responsible for ensuring that our products are manufactured according to our marketing authorisations and GMP. Together with your competent and experienced colleagues you will be responsible for qualification and validation of, among others, equipment, utility and existing facility. This includes handling of non-conformities and change control cases as well as approval of instructions. Furthermore, you will also participate in project work related to expansion of our growth hormone production.
In your daily work, you will interact with colleagues in the production department, and your success will depend on your ability to collaborate and communicate with all types of people in a positive and constructive way. Quality is the key word in this job and therefore it is natural for you to have an on-going dialogue with your colleagues regarding how we ensure quality and compliance, improve our operations and avoid errors.
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.
Qualifications
You are a qualified engineer, pharmacist or have a Master of Science degree. Preferable your academic background is topped with experience from the pharmaceutical industry within qualification and validation. However, we would also like to hear from talented newly academic graduates.
You have a strong quality mind-set, meet your deadlines, and know how to prioritise between different tasks in a dynamic environment. Your language skills cover proficiency in both Danish and English, and you have experience with GMP and the requirements of the authorities in the pharmaceutical industry.
As a person, you are known for a high commitment to finding constructive solutions as well as taking responsibility for your assignments. You work independently and you are not afraid of making decisions regarding quality tasks and ensure the right balance between quality demands, authority demands and business needs. At the same time, you perform well in a team-oriented environment. Feel free to submit your job application in either English or Danish, whichever you prefer. Applications are reviewed on a rolling basis so please apply as soon as possible.
At Novo Nordisk it is your skills, your commitment and your ambitions, which help us to improve many people’s lives. In return we offer you the opportunity to work with talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information, please call associate manager Lotte Solvang Christensen on +45 3075 8846.
Deadline
29 June 2014
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QA Professional – for 18 Months temporary vacancy
- Quality
- Denmark - Gentofte
Would you like to join us in making a difference to people with growth hormone deficiency? Would you like to be responsible for quality assurance of qualification and validation tasks? If the answer is yes, Biopharm QA API Gentofte is looking for a talented and ambitious QA Professional for a temporary position.
About the department
Biopharm QA API is a dynamic department with 35 people, divided into 3 teams who are responsible for the quality assurance of API for marketed pharmaceutical products.
We are currently expanding our department and have an open positions in our Facility team. You will become part of a well-functioning, self-steering team with 7 dedicated colleagues. You will be responsible for the technical part of quality assurance. The working relations are informal and helpful and the team values professional sparring and good humour highly.
The Job
As a QA professional you will be responsible for ensuring that our products are manufactured according to our marketing authorisations and GMP. Together with your competent and experienced colleagues you will be responsible for qualification and validation of, among others, equipment, utility and existing facility. This includes handling of non-conformities and change control cases as well as approval of instructions. Furthermore, you will also participate in project work related to expansion of our growth hormone production.
In your daily work, you will interact with colleagues in the production department, and your success will depend on your ability to collaborate and communicate with all types of people in a positive and constructive way. Quality is the key word in this job and therefore it is natural for you to have an on-going dialogue with your colleagues regarding how we ensure quality and compliance, improve our operations and avoid errors.
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.
Qualifications
You are a qualified engineer, pharmacist or have a Master of Science degree. Preferable your academic background is topped with experience from the pharmaceutical industry within qualification and validation. However, we would also like to hear from talented newly academic graduates.
You have a strong quality mind-set, meet your deadlines, and know how to prioritise between different tasks in a dynamic environment. Your language skills cover proficiency in both Danish and English, and you have experience with GMP and the requirements of the authorities in the pharmaceutical industry.
As a person, you are known for a high commitment to finding constructive solutions as well as taking responsibility for your assignments. You work independently and you are not afraid of making decisions regarding quality tasks and ensure the right balance between quality demands, authority demands and business needs. At the same time, you perform well in a team-oriented environment. Feel free to submit your job application in either English or Danish, whichever you prefer. Applications are reviewed on a rolling basis so please apply as soon as possible.
At Novo Nordisk it is your skills, your commitment and your ambitions, which help us to improve many people’s lives. In return we offer you the opportunity to work with talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information, please call associate manager Lotte Solvang Christensen on +45 3075 8846.
Deadline
29 June 2014
Search all jobs at Novo Nordisk
Please select
Country Denmark (93) USA () China (322) Canada (4) Field Based (7) India - Karnataka (2) Japan (1) Malaysia (1) Sweden (1) Switzerland (2) West Sussex (4)
Connect with us
Email job agent
