Senior QA Professional for Qualification in Aseptic Production
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Bagsværd
At Injectable Finished Products (IFP) QA Bagsværd we are responsible for quality assurance of the aseptic production in Bagsværd. It is our responsibility to ensure that the documentation meets the regulatory GMP requirements. IFP QA Bagsværd consists of 50 dedicated and engaged employees who are divided into four different teams – Operations, AP release, QA release and Project Qualification team.
We are looking for a new colleague to join our Project Qualification Team.
The job
Your key responsibility is to ensure that validation of production processes, as well as qualification of facilities, equipment and automation systems is documented according to current GMP requirements. You will do this by involvement in investment and optimization projects, as well as your daily support to production. Your daily tasks will also include approval of deviations, change requests and SOPs. Also, you will participate in problem solving alongside our colleagues in the production, as we are present in the production every day to secure QA oversight. As Senior QA professional, you will play a central role where you need to make decisions and set directions for Quality. This demands good collaboration skills and a solution-oriented approach when collaborating with colleagues both in the production and QA.
We work together as a team with a desire to solve challenges through open and honest dialogue. We always work on improving our way of working and we appreciate new ideas and continues improvements.
Qualifications
Ideally, you have minimum 4 years of experience from QA or pharmaceutical production, and a Master´s degree in Engineering, Pharmacy or corresponding education (for example MSc. Biochemistry or Operation and Maintenance Engineering). Technical knowledge regarding aseptic production equipment and automation, as well as experience with risk assessment and qualification /validation is an advantage
As a person it is natural for you to solve challenges in collaboration with colleagues and seek feedback on your assignments to ensure the best possible solution. You have the right quality mindset, dare to challenge our way of working and are known for your ability to identify improvements, as well as taking the lead for driving the implementation of these improvements. You are open, honest and inclusive regarding your QA and production colleagues, and enjoy working in a dynamic environment where you can take responsibility.
You are ambitious and ready to be part of our on-going effort to improve our high standards, including ensuring new ways of working are implemented smoothly. We operate in an international company and the position therefore requires proficiency in English – Danish will be an advantage.
Working at Novo Nordisk
At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and more than 371 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.
Contact
For further information, contact Thinnakone Arounsack-Jørgensen on +45 3079 6154.
Deadline
16th January 2023
Feel free to submit your application in Danish or English. Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate has been identified.
To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
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We are looking for a new colleague to join our Project Qualification Team.
The job
Your key responsibility is to ensure that validation of production processes, as well as qualification of facilities, equipment and automation systems is documented according to current GMP requirements. You will do this by involvement in investment and optimization projects, as well as your daily support to production. Your daily tasks will also include approval of deviations, change requests and SOPs. Also, you will participate in problem solving alongside our colleagues in the production, as we are present in the production every day to secure QA oversight. As Senior QA professional, you will play a central role where you need to make decisions and set directions for Quality. This demands good collaboration skills and a solution-oriented approach when collaborating with colleagues both in the production and QA.
We work together as a team with a desire to solve challenges through open and honest dialogue. We always work on improving our way of working and we appreciate new ideas and continues improvements.
Qualifications
Ideally, you have minimum 4 years of experience from QA or pharmaceutical production, and a Master´s degree in Engineering, Pharmacy or corresponding education (for example MSc. Biochemistry or Operation and Maintenance Engineering). Technical knowledge regarding aseptic production equipment and automation, as well as experience with risk assessment and qualification /validation is an advantage
As a person it is natural for you to solve challenges in collaboration with colleagues and seek feedback on your assignments to ensure the best possible solution. You have the right quality mindset, dare to challenge our way of working and are known for your ability to identify improvements, as well as taking the lead for driving the implementation of these improvements. You are open, honest and inclusive regarding your QA and production colleagues, and enjoy working in a dynamic environment where you can take responsibility.
You are ambitious and ready to be part of our on-going effort to improve our high standards, including ensuring new ways of working are implemented smoothly. We operate in an international company and the position therefore requires proficiency in English – Danish will be an advantage.
Working at Novo Nordisk
At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and more than 371 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.
Contact
For further information, contact Thinnakone Arounsack-Jørgensen on +45 3079 6154.
Deadline
16th January 2023
Feel free to submit your application in Danish or English. Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate has been identified.
To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Print job Send to e-mail
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 15.12.2022, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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