Quality Assurance Professional needed for an API facility in Kalundborg
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Kalundborg
Are you motivated by working with highly competent and helpful colleagues which, as a team, has the responsibility of ensuring API production of biological products in Kalundborg? Does working with haemophilia products which are crucial for patients sound interesting ? Then you are on the way to a unique job as QA for Biotech and Rare Disease API.
About the department
We are 50 employees in the department covering production of API in BRD in all of Denmark, with production sites in Hillerød, Kalundborg and Gentofte. The team you will be part of consists of 12 employees with primary base in Kalundborg. We are a dynamic and well-functioning department with a lot of interfaces in the organisation including productions, management, manufacturing development and other QA departments. We love academic challenges and work with a lot of individual responsibility together with a high engagement. Social responsibility is a priority in the department – it has to be fun and challenging to go to work.
The Job
In the job, you will need to use your talents to secure the delivery of our products and this requires us to do our utmost every day, to ensure that we meet the ever-increasing demands from customers and authorities.
Our main responsibility is to set the direction for quality and compliance due to internal and external requirements. We are offering an exciting and challenging role where you will become a part of a competent and solution-oriented team which works as a sparring partner and problem solver regarding quality issues in the production.
Your main responsibilities will be:
In this job you will truly get the opportunity to make an impact with your decisions, initiatives and engagement - we have a positive working environment and strive to solve challenges through an open and honest dialog.
Qualification
We expect you to have:
As a person you are outgoing, analytical, flexible, proactive and engaged about your assignments. You welcome new ideas and new ways of working and have great collaboration and communication skills. You meet all deadlines with a structured approach and maintain the overview – even in a busy environment where priorities can change quickly.
About Novo Nordisk
At Novo Nordisk, we use our competencies, dedication, and ambitions to help many people improve their lives. At the same time, we offer the opportunity to become part of a global workplace where you work with talented colleagues and where your passion and commitment are met with opportunities for personal and professional development.
Contact
If you want to know more about the job, contact Mie Rishede +45 3075 7859.
Deadline
27. November 2022, interviews will be held continuously.
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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About the department
We are 50 employees in the department covering production of API in BRD in all of Denmark, with production sites in Hillerød, Kalundborg and Gentofte. The team you will be part of consists of 12 employees with primary base in Kalundborg. We are a dynamic and well-functioning department with a lot of interfaces in the organisation including productions, management, manufacturing development and other QA departments. We love academic challenges and work with a lot of individual responsibility together with a high engagement. Social responsibility is a priority in the department – it has to be fun and challenging to go to work.
The Job
In the job, you will need to use your talents to secure the delivery of our products and this requires us to do our utmost every day, to ensure that we meet the ever-increasing demands from customers and authorities.
Our main responsibility is to set the direction for quality and compliance due to internal and external requirements. We are offering an exciting and challenging role where you will become a part of a competent and solution-oriented team which works as a sparring partner and problem solver 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 will truly get the opportunity to make an impact with your decisions, initiatives and engagement - we have a positive working environment and strive 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
- The ability to make decisions based on your GMP knowledge and experience
- Fluency in reading Danish and great oral communication skills in both English and Danish
As a person you are outgoing, analytical, flexible, proactive and engaged about your assignments. You welcome new ideas and new ways of working and have great collaboration and communication skills. You meet all deadlines with a structured approach and maintain the overview – even in a busy environment where priorities can change quickly.
About Novo Nordisk
At Novo Nordisk, we use our competencies, dedication, and ambitions to help many people improve their lives. At the same time, we offer the opportunity to become part of a global workplace where you work with talented colleagues and where your passion and commitment are met with opportunities for personal and professional development.
Contact
If you want to know more about the job, contact Mie Rishede +45 3075 7859.
Deadline
27. November 2022, interviews will be held continuously.
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 Kalundborg.
Jobbet er oprettet på vores service den 2.11.2022, 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.
- Øvrige
- Kalundborg
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