QA Professional

Quality Assurance Professional 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 QA (Quality Assurance) for Biotech and Rare Disease API (Active Pharmaceutical Ingredient). 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 in the production. Your main responsibilities will be:

Reviewing e.g. batch documentation, trend reports, SOPs, deviations and validation documentations.

QA presence; being physically present in the production to observe performed processes and help solve issues in real time.

In this job you really will get the opportunity to make an impact with your decisions, initiatives and engagement - We have a positive working environment with a wish to solve challenges through an open and honest dialog. Qualification
We expect you to:

Have an academic degree within Ms. Pharmacy, veterinarian, microbiology or similar.

Has the ability to make decisions based on your GMP knowledge and experience.

be fluent in reading Danish and communication skills in both English and Danish.

Are keen to learn about various IT systems in optimizing processes and in daily work

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 60 employees in the department covering production of API in all of Denmark, with production sites in Hillerød, Kalundborg and Gentofte. The team you will be part of have primary base in Kalundborg. We are a dynamic and well-functioning department with a lot of interfaces in the organisation. We love academic challenges and work with a big individual responsibility together with a high engagement. Social responsibility is a priority in the department – it needs to be fun and challenging to go to work.

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 Mie Rishede +45 3075 7859.

Deadline 31. July 2023 – Applications will be evaluated continuously, and candidates may be called for interview before the deadline, so please apply as soon as you can. You do not need to attach a cover letter to your application, but please include a few lines about your motivation in your resume or CV. Additionally, please avoid the use of photos in your CV. This provides a better and more fair process. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. Quality Assurance Professional 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 QA (Quality Assurance) for Biotech and Rare Disease API (Active Pharmaceutical Ingredient). 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 in the production. Your main responsibilities will be:

Reviewing e.g. batch documentation, trend reports, SOPs, deviations and validation documentations.

QA presence; being physically present in the production to observe performed processes and help solve issues in real time.

In this job you really will get the opportunity to make an impact with your decisions, initiatives and engagement - We have a positive working environment with a wish to solve challenges through an open and honest dialog. Qualification
We expect you to:

Have an academic degree within Ms. Pharmacy, veterinarian, microbiology or similar.

Has the ability to make decisions based on your GMP knowledge and experience.

be fluent in reading Danish and communication skills in both English and Danish.

Are keen to learn about various IT systems in optimizing processes and in daily work

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 60 employees in the department covering production of API in all of Denmark, with production sites in Hillerød, Kalundborg and Gentofte. The team you will be part of have primary base in Kalundborg. We are a dynamic and well-functioning department with a lot of interfaces in the organisation. We love academic challenges and work with a big individual responsibility together with a high engagement. Social responsibility is a priority in the department – it needs to be fun and challenging to go to work.

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 Mie Rishede +45 3075 7859.

Deadline 31. July 2023 – Applications will be evaluated continuously, and candidates may be called for interview before the deadline, so please apply as soon as you can. You do not need to attach a cover letter to your application, but please include a few lines about your motivation in your resume or CV. Additionally, please avoid the use of photos in your CV. This provides a better and more fair process. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 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.