Senior QA Specialist for Global Contract Manufacturing
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Søborg
Do you want to be part of expanding our Drug Substance (DS) capacity by using Contract Manufacturing Organizations (CMOs)? Do you want to work in one of the most interesting and fast-growing areas in Novo Nordisk and eager to take your professional carrier to the next step?
Then, join us in shaping the future of Quality Assurance and making a global impact in pharmaceutical manufacturing!
The position
As a Senior QA Specialist, together with a highly skilled team, you will be responsible for building the Quality mind-set and Quality and Compliance culture at the CMOs and work with our colleagues in Line-of-Business to ensure highest quality at our CMOs production.
Main responsibilities will include:
• ensuring that Global Contract Manufacturing (GCM) DS QA are ready for inspection
• developing a set-up to evaluate findings at CMOs
• taking an active role in training in requirements across different QA areas
• participating in selection of new CMOs
As most of the CMOs are located outside Denmark there will be some traveling in this job. Qualifications
We are looking for a colleague with a well-developed Quality mind-set and an ability to set direction, engage and energize employees in the tasks and challenges at hand.
To succeed in this role, you:
• hold a masters ‘ degree within Pharmacy, Chemistry, Biotechnology Engineering, Science or similar
• are a skilled QA specialist with business understanding within CMOs
• preferably have several years of relevant experience working with raw materials or drug substance
• can drive and inspire others
• are fully proficient in English
As a person, you have a high level of energy and drive, are open-minded and positive attitude, want to make a difference and are eager to learn. You can understand and collaborate in an international environment with respect for cultural differences, as you will be operating in said environment, sometimes proving to be cultural and politically challenging.
Finally, you are diplomatic and have a mature appearance and style which demonstrates authority and good judgement.
About the department
GCM DS QA is part of the Quality organization in Product Supply, Novo Nordisk A/S. We are responsible for Quality Assurance of CMOs producing raw material and drug substance on behalf of Novo Nordisk. It’s our responsibility to ensure that CMOs are selected based on a thorough assessment, and supporting them in the project phase ready for Process Validation and in the operational phase.
The job is in Søborg, Denmark but from end 2024 we will move to Høje Tåstrup just next the train station.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
For further information, please contact Vice President Trine Kantsø +45 30794362.
Deadline
3 March 2024
We will review applications received on an ongoing basis, so do not hesitate to apply today.
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.
Then, join us in shaping the future of Quality Assurance and making a global impact in pharmaceutical manufacturing!
The position
As a Senior QA Specialist, together with a highly skilled team, you will be responsible for building the Quality mind-set and Quality and Compliance culture at the CMOs and work with our colleagues in Line-of-Business to ensure highest quality at our CMOs production.
Main responsibilities will include:
• ensuring that Global Contract Manufacturing (GCM) DS QA are ready for inspection
• developing a set-up to evaluate findings at CMOs
• taking an active role in training in requirements across different QA areas
• participating in selection of new CMOs
As most of the CMOs are located outside Denmark there will be some traveling in this job. Qualifications
We are looking for a colleague with a well-developed Quality mind-set and an ability to set direction, engage and energize employees in the tasks and challenges at hand.
To succeed in this role, you:
• hold a masters ‘ degree within Pharmacy, Chemistry, Biotechnology Engineering, Science or similar
• are a skilled QA specialist with business understanding within CMOs
• preferably have several years of relevant experience working with raw materials or drug substance
• can drive and inspire others
• are fully proficient in English
As a person, you have a high level of energy and drive, are open-minded and positive attitude, want to make a difference and are eager to learn. You can understand and collaborate in an international environment with respect for cultural differences, as you will be operating in said environment, sometimes proving to be cultural and politically challenging.
Finally, you are diplomatic and have a mature appearance and style which demonstrates authority and good judgement.
About the department
GCM DS QA is part of the Quality organization in Product Supply, Novo Nordisk A/S. We are responsible for Quality Assurance of CMOs producing raw material and drug substance on behalf of Novo Nordisk. It’s our responsibility to ensure that CMOs are selected based on a thorough assessment, and supporting them in the project phase ready for Process Validation and in the operational phase.
The job is in Søborg, Denmark but from end 2024 we will move to Høje Tåstrup just next the train station.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
For further information, please contact Vice President Trine Kantsø +45 30794362.
Deadline
3 March 2024
We will review applications received on an ongoing basis, so do not hesitate to apply today.
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.
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 20.2.2024, 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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