Senior QA Validation Professional
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Gentofte
Would you like to be part of QA projects? Do you thrive in having interactions with many stakeholders internally a well as with external vendors. Are you motivated by finding ways through the jungle of cGMP (Current Good Manufacturing Practice), optimization projects and securing delivery of vital medicine to patients? Would you like to be part of an excellent team where “together” and “having fun” are key essentials? Then you are on the way to a unique job as validation QA for Biotech and Rare Disease – aseptic production. Read more below and apply!
The position
Our main responsibility is to set direction for quality and compliance due to internal and external requirements. We are offering an exciting and challenging job where you will become part of a competent and solution-oriented team, which works as sparring and problem solvers regarding quality issues regarding primarily validation and qualifications. Both in the exciting production facility but also very much ensuring good quality for our two new filling lines which we are currently building.
Some of your main responsibilities will be:
• Setting direction regarding qualification requirements in ongoing and new projects
• Reviewing and approving validation and qualification documentations and change requests
• Interaction with external vendors in and outside of Denmark
In this role you really will get the opportunity to make an impact with your decisions, initiatives and engagement, given that we are also overseeing the implementation of two new lines in our facility.
We have a positive working environment with a wish to solve challenges through an open and honest dialog.
The job is located in Gentofte but some travel might be required.
Qualifications
We are looking for someone that has experience with GMP (Good Manufacturing Practice) and is outgoing and passionate about assignments.
In order to succeed in this role, you:
• Have a Master’s degree (preferably in Engineering, Pharmacy, Veterinarian or Microbiology)
• Have QA experience in a pharma environment
• Are keen to learn about various IT systems in optimizing processes and in daily work
• Are fluent in English and having some understanding of Danish will be preferrable
If you also have previous validation experience that will be an advantage.
On a personal note, you welcome new ideas and new ways of working and have good collaboration and communication skills. Your good at narrowing the problem down to the essentials and finding good solutions to problems – even in a busy environment where priorities can change quickly for the benefit of patients.
About the department
We are a dynamic and well-functioning department with many interfaces around the organization including production, management and other QA departments. We love professional challenges and work independently with great individual responsibility, while a high level of commitment and good socializing is in focus – it must be fun and challenging to go to work.
We are around 50 employees in the department, where you will be part of a team consisting of 8 highly skilled and competent colleagues. You will become part of an ambitious team with good humour in a casual atmosphere and where we take care of each other. We are open and honest and appreciate a colleague who takes responsibility and have a positive approach to new challenges.
About 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
If you want to know more about the job, contact Randi Muren +45 3075 0680
Deadline
21 November 2022
Please note that interviews will be held continuously.
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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The position
Our main responsibility is to set direction for quality and compliance due to internal and external requirements. We are offering an exciting and challenging job where you will become part of a competent and solution-oriented team, which works as sparring and problem solvers regarding quality issues regarding primarily validation and qualifications. Both in the exciting production facility but also very much ensuring good quality for our two new filling lines which we are currently building.
Some of your main responsibilities will be:
• Setting direction regarding qualification requirements in ongoing and new projects
• Reviewing and approving validation and qualification documentations and change requests
• Interaction with external vendors in and outside of Denmark
In this role you really will get the opportunity to make an impact with your decisions, initiatives and engagement, given that we are also overseeing the implementation of two new lines in our facility.
We have a positive working environment with a wish to solve challenges through an open and honest dialog.
The job is located in Gentofte but some travel might be required.
Qualifications
We are looking for someone that has experience with GMP (Good Manufacturing Practice) and is outgoing and passionate about assignments.
In order to succeed in this role, you:
• Have a Master’s degree (preferably in Engineering, Pharmacy, Veterinarian or Microbiology)
• Have QA experience in a pharma environment
• Are keen to learn about various IT systems in optimizing processes and in daily work
• Are fluent in English and having some understanding of Danish will be preferrable
If you also have previous validation experience that will be an advantage.
On a personal note, you welcome new ideas and new ways of working and have good collaboration and communication skills. Your good at narrowing the problem down to the essentials and finding good solutions to problems – even in a busy environment where priorities can change quickly for the benefit of patients.
About the department
We are a dynamic and well-functioning department with many interfaces around the organization including production, management and other QA departments. We love professional challenges and work independently with great individual responsibility, while a high level of commitment and good socializing is in focus – it must be fun and challenging to go to work.
We are around 50 employees in the department, where you will be part of a team consisting of 8 highly skilled and competent colleagues. You will become part of an ambitious team with good humour in a casual atmosphere and where we take care of each other. We are open and honest and appreciate a colleague who takes responsibility and have a positive approach to new challenges.
About 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
If you want to know more about the job, contact Randi Muren +45 3075 0680
Deadline
21 November 2022
Please note that interviews will be held continuously.
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 Gentofte.
Jobbet er oprettet på vores service den 28.10.2022, 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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- Gentofte
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Statistik over udbudte øvrige i Gentofte over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 3. november 2024 | 19 |
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| 4. oktober 2024 | 22 |