Qualification Professional
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Are you seeking new professional challenges within tablet-formulation and production? Do you also think that it is meaningful to make a difference for patients with diabetes?
Then here at Oral Finish Products (OFP) we have the right opportunity for you, read more and apply!
About The Department
In OFP we set ourselves the ambitious goal of being the first on the market with a tablet containing a GLP-1 based drug. A fantastic accomplishment that was just achieved as the product has gained approval in several markets worldwide including the USA and Europe. We are extremely proud that we finally offer patients with type 2 diabetes an alternative to the injectable preparations - an oral product in tablet form.
You will join the manufacturing development, which consists of about 70 colleagues split across 5 different teams. The department’s purpose is deliveries related to the latest clinical phases such as qualification of equipment, development and validation of production processes as well as pilot production in a GMP environment.
The department is also responsible for contributing with documentation to the authorities, when applying for registrations.
The position
In OFP we do our best for you as a new member to get the best possible start in your new job. The first days, you will spend with your new colleagues, where you together will go through an exciting introduction. The area manager will welcome you and a colleague from your own team will act as a mentor and walk you through your individual training plan. We know how important it is, and we are looking forward to meeting you.
On a daily basis you can expect to:
• be responsible for qualifications of process equipment for the tablet production such as mixers, tablet machines and In Process Control equipment
• solve practical and documental qualification tasks, such as writing change requests and instructions
• develop yourself in the role as equipment qualifier
• work according to lean principles and GMP regulations
Qualifications
We are looking for someone who keeps a good overview and like being where things are happening, honoring collaborations with various workgroups such as operators, technicians, chemists, production line leaders as well as external partners.
To succeed in this role you:
• hold a bachelor or master’s degree in a technical or scientific field
• have experience in the pharmaceutical industry
• have extensive knowledge of GMP-rules
• have experience with qualification and/or operation of facilities
• are proficient in English
Some knowledge of Danish, especially written, will be considered beneficial but it is not required.
If you don't have experience but posses the right education we might consider you as a Trainee; in this position you will work closely with an experienced prosfessional that will guide you through the fundamentals of the job for around a year.
On a personal level you prefer to work in a dynamic environment and manage to make decisions that does not compromise quality or work environment, taking responsibility for your tasks with a sense for details.
When you need help, you are not afraid to ask, and you are happy to share your own experiences. You believe that results are best achieved by strong teamwork and you never compromise on your quality of work.
Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.
Contact
For more information, please contact team leader Jimmie Slot Madsen on +45 3079 5992
Deadline
20 January 2023
Please note that interviews will be held continuously so we encourage you not to wait for the deadline to apply.
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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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Then here at Oral Finish Products (OFP) we have the right opportunity for you, read more and apply!
About The Department
In OFP we set ourselves the ambitious goal of being the first on the market with a tablet containing a GLP-1 based drug. A fantastic accomplishment that was just achieved as the product has gained approval in several markets worldwide including the USA and Europe. We are extremely proud that we finally offer patients with type 2 diabetes an alternative to the injectable preparations - an oral product in tablet form.
You will join the manufacturing development, which consists of about 70 colleagues split across 5 different teams. The department’s purpose is deliveries related to the latest clinical phases such as qualification of equipment, development and validation of production processes as well as pilot production in a GMP environment.
The department is also responsible for contributing with documentation to the authorities, when applying for registrations.
The position
In OFP we do our best for you as a new member to get the best possible start in your new job. The first days, you will spend with your new colleagues, where you together will go through an exciting introduction. The area manager will welcome you and a colleague from your own team will act as a mentor and walk you through your individual training plan. We know how important it is, and we are looking forward to meeting you.
On a daily basis you can expect to:
• be responsible for qualifications of process equipment for the tablet production such as mixers, tablet machines and In Process Control equipment
• solve practical and documental qualification tasks, such as writing change requests and instructions
• develop yourself in the role as equipment qualifier
• work according to lean principles and GMP regulations
Qualifications
We are looking for someone who keeps a good overview and like being where things are happening, honoring collaborations with various workgroups such as operators, technicians, chemists, production line leaders as well as external partners.
To succeed in this role you:
• hold a bachelor or master’s degree in a technical or scientific field
• have experience in the pharmaceutical industry
• have extensive knowledge of GMP-rules
• have experience with qualification and/or operation of facilities
• are proficient in English
Some knowledge of Danish, especially written, will be considered beneficial but it is not required.
If you don't have experience but posses the right education we might consider you as a Trainee; in this position you will work closely with an experienced prosfessional that will guide you through the fundamentals of the job for around a year.
On a personal level you prefer to work in a dynamic environment and manage to make decisions that does not compromise quality or work environment, taking responsibility for your tasks with a sense for details.
When you need help, you are not afraid to ask, and you are happy to share your own experiences. You believe that results are best achieved by strong teamwork and you never compromise on your quality of work.
Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.
Contact
For more information, please contact team leader Jimmie Slot Madsen on +45 3079 5992
Deadline
20 January 2023
Please note that interviews will be held continuously so we encourage you not to wait for the deadline to apply.
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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 Måløv.
Jobbet er oprettet på vores service den 28.11.2022, 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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