Advanced QA Professional in Global Contract Manufacturing QA
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Søborg
Would you like to work in one of the most interesting, complex and dynamic areas in Novo Nordisk? Are you ready to engage, support and mobilise colleagues in an international business environment, to make a difference for people living with disease like diabetes and haemophilia? Then you could be our new colleague in GCM QA, Bagsværd offering you personal and professional development and training, if needed. Global Contract Manufacturing (GCM) QA is responsible for quality assurance and quality support for outsourced production activities worldwide.
The position
You will have the opportunity to make a difference for thousands of patients around the world by ensuring a high level of quality of the products of Novo Nordisk.
As QA Professional you will be responsible for quality assurance of contract manufacturing. You will have to offer QA support and GMP guidance to our partners and do the final release of tablets and packaging from CMO's to the further process in Novo Nordisk. Also, you will be responsible for ensuring that our products are manufactured according to cGMP and our marketing authorisations.
You will have numerous encounters daily with both internal and external business partners and you should expect a high level of complexity in your daily tasks. You will solve a wide variety of tasks and have a great opportunity to be challenged every day. The daily QA activities are typically carried out by the contract manufacturers themselves, but the handling of documentation from the contract manufacturers is a part of the job.
Since the manufacturers are located outside Denmark, you are expected to travel 5-10 days a year.
Qualifications
You hold an academic degree as Pharmacist, Engineer or similar and have at least 4 years of experience from a pharmaceutical organisation where you have gained a solid and up-to-date knowledge of quality and GMP requirements i.e. Deviations (DV), Corrective Actions and Preventive Actions (CAPA) handling, change control, complaints, Annual Product Review (APR) and validations.
The ideal candidate is Qualified Person (QP) delegate and/or has thorough knowledge of quality assurance of pharmaceutical manufactured products within tablets and packaging.
With your good cooperation and communication skills you are able to organise and drive tasks. You have a pragmatic approach to problem solving and strong interpersonal skills. You are detail-oriented with a strong quality mind set and are a team player but are also able to work independently. You thrive on working across departments in an international organisation. Great communication skills are a must, and you are expected to be fluent in Danish and English.
We are looking for an open-minded person with an outgoing attitude and natural networking skills. Additionally, we would enjoy welcoming a straightforward person with a good sense of humour to our department.
About the department
GCM QA is a dynamic department consisting of around 45 competent people and is characterised by a high level of professionalism, flexibility and cooperation. The primary role of our department is to deliver QA support and set direction for our Global Contract Manufacturer Organisations worldwide. The open position as experienced QA is in the GCM QA DP Operations team, which is responsible for aseptic production, tablets and packaging at the CMO´s. Working at Novo Nordisk
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Christophe Poirel Madsen on +45 3077 6827.
Deadline
8th of May 2023 You do not need to attach a cover letter to your application, but please include a few sentences about your motivation 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.
The position
You will have the opportunity to make a difference for thousands of patients around the world by ensuring a high level of quality of the products of Novo Nordisk.
As QA Professional you will be responsible for quality assurance of contract manufacturing. You will have to offer QA support and GMP guidance to our partners and do the final release of tablets and packaging from CMO's to the further process in Novo Nordisk. Also, you will be responsible for ensuring that our products are manufactured according to cGMP and our marketing authorisations.
You will have numerous encounters daily with both internal and external business partners and you should expect a high level of complexity in your daily tasks. You will solve a wide variety of tasks and have a great opportunity to be challenged every day. The daily QA activities are typically carried out by the contract manufacturers themselves, but the handling of documentation from the contract manufacturers is a part of the job.
Since the manufacturers are located outside Denmark, you are expected to travel 5-10 days a year.
Qualifications
You hold an academic degree as Pharmacist, Engineer or similar and have at least 4 years of experience from a pharmaceutical organisation where you have gained a solid and up-to-date knowledge of quality and GMP requirements i.e. Deviations (DV), Corrective Actions and Preventive Actions (CAPA) handling, change control, complaints, Annual Product Review (APR) and validations.
The ideal candidate is Qualified Person (QP) delegate and/or has thorough knowledge of quality assurance of pharmaceutical manufactured products within tablets and packaging.
With your good cooperation and communication skills you are able to organise and drive tasks. You have a pragmatic approach to problem solving and strong interpersonal skills. You are detail-oriented with a strong quality mind set and are a team player but are also able to work independently. You thrive on working across departments in an international organisation. Great communication skills are a must, and you are expected to be fluent in Danish and English.
We are looking for an open-minded person with an outgoing attitude and natural networking skills. Additionally, we would enjoy welcoming a straightforward person with a good sense of humour to our department.
About the department
GCM QA is a dynamic department consisting of around 45 competent people and is characterised by a high level of professionalism, flexibility and cooperation. The primary role of our department is to deliver QA support and set direction for our Global Contract Manufacturer Organisations worldwide. The open position as experienced QA is in the GCM QA DP Operations team, which is responsible for aseptic production, tablets and packaging at the CMO´s. Working at Novo Nordisk
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Christophe Poirel Madsen on +45 3077 6827.
Deadline
8th of May 2023 You do not need to attach a cover letter to your application, but please include a few sentences about your motivation 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.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 18.4.2023, 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
- Søborg
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