Experienced QA for QC to Global Contract Manufacturing projects
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Are you keen on playing a crucial role in ensuring and overseeing Quality Control processes in our global network of Contract Manufacturer Organisations (CMOs)? Do you thrive in a job with lots of professional interfaces working with projects with many stakeholders?
Then this is a great opportunity to become a part of one of Novo Nordisk’s most attractive and interesting QA teams. We come to work (or work from home) with a smile on our faces and we go home with the knowledge that we have made a difference for Novo Nordisk, our customers, and our colleagues.
The position
In this position you will be QA responsible for the analytical method transfer from Novo Nordisk to CMOs. Your key task will be to ensure the quality of processes, analysis and methods related to testing of outsourced raw materials, intermediates, drug substances, and drug products. You will participate in various projects working with both internal and external business partners and you must expect a high level of complexity and independent decision making in your daily tasks.
The job includes QA review of several types of documents such as protocols and reports for method validation, change requests and deviations. The analyses performed are chemical, physical and general pharmacopeia methods including microbiology. Your role will also include oversight of external laboratories as part of assessments, audits and projects to ensure that the products delivered to Novo Nordisk are analysed in full compliance with the current practice and expectations from authorities.
Since the manufacturers are located outside Denmark you are expected to travel around 10 days a year as your experience and hands-on knowledge is sometimes needed in other parts of our global organisation.
If you are looking for a job which can foster the development of your professional and personal competences, this may be your opportunity.
Qualifications
You hold an academic degree as Pharmacist, Chemist, Engineer or similar and have at least 1 year of experience with QC method validation
In addition,
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 responsible for quality assurance and quality support to outsourced production activities worldwide.
GCM QA is a dynamic department consisting of 40 competent people divided into 4 teams with focus on either operations or projects. You will be a strong player in the project teams. The department 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 CMOs.
We focus on good social relations and prioritise to make room for fun at work. We have weekly quizzes, and we strive to have daily workout sessions to ensure on-going well-being in the team.
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 Pia Bech Vince on +45 3079 2171.
Deadline
Please send your application before 5th January 2023.
We will review applications and perform interviews on an ongoing basis, so you are encouraged to apply as soon as possible.
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.
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Then this is a great opportunity to become a part of one of Novo Nordisk’s most attractive and interesting QA teams. We come to work (or work from home) with a smile on our faces and we go home with the knowledge that we have made a difference for Novo Nordisk, our customers, and our colleagues.
The position
In this position you will be QA responsible for the analytical method transfer from Novo Nordisk to CMOs. Your key task will be to ensure the quality of processes, analysis and methods related to testing of outsourced raw materials, intermediates, drug substances, and drug products. You will participate in various projects working with both internal and external business partners and you must expect a high level of complexity and independent decision making in your daily tasks.
The job includes QA review of several types of documents such as protocols and reports for method validation, change requests and deviations. The analyses performed are chemical, physical and general pharmacopeia methods including microbiology. Your role will also include oversight of external laboratories as part of assessments, audits and projects to ensure that the products delivered to Novo Nordisk are analysed in full compliance with the current practice and expectations from authorities.
Since the manufacturers are located outside Denmark you are expected to travel around 10 days a year as your experience and hands-on knowledge is sometimes needed in other parts of our global organisation.
If you are looking for a job which can foster the development of your professional and personal competences, this may be your opportunity.
Qualifications
You hold an academic degree as Pharmacist, Chemist, Engineer or similar and have at least 1 year of experience with QC method validation
In addition,
- You have a solid and up-to date knowledge of quality and GMP requirements
- You take responsibility, work independently and make decisions that balance quality demands, authority expectations and business needs.
- You meet your deadlines, and you know how to prioritise between different tasks in an everchanging environment.
- You have the ability to work in an international set-up with external stakeholders with different interests and agendas
- You have great communication and collaboration skills 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 responsible for quality assurance and quality support to outsourced production activities worldwide.
GCM QA is a dynamic department consisting of 40 competent people divided into 4 teams with focus on either operations or projects. You will be a strong player in the project teams. The department 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 CMOs.
We focus on good social relations and prioritise to make room for fun at work. We have weekly quizzes, and we strive to have daily workout sessions to ensure on-going well-being in the team.
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 Pia Bech Vince on +45 3079 2171.
Deadline
Please send your application before 5th January 2023.
We will review applications and perform interviews on an ongoing basis, so you are encouraged to apply as soon as possible.
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.
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 Bagsværd.
Jobbet er oprettet på vores service den 18.10.2022, 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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