Senior Quality Advisor
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Søborg
Do you dream of using your great quality mind-set in a highly professional and engaged global environment? Would you like to work in an exciting environment with ample opportunities for personal development and frequent interaction with diverse stakeholders across Development and Research & Early Development. Then this could be an interesting opportunity for you! Apply today and join us as our new Senior Quality Advisor.
About the department
The open position is in Quality Management System (QMS) Operations department in R&D Quality, located in Søborg. In QMS Operations we are responsible for our QMS, we provide Quality support and assurance to our stakeholders.
We are also responsible for coordinating Quality Management Review (QMR) at senior management levels in order to get an overview of the current quality performance, ensure adequacy of the QMS, and ensure quality performance going forward.
Research and Development (R&D) Quality is part of Development organisation and we play a vital role in supporting the drug and device development process to ensure high quality as well as fit-for-purpose processes. In Novo Nordisk, we have an ambitious drug and device development program and we work in a global setting with focus on delivering viable products that make a difference to patients and ultimately benefit society.
The position
The main responsibilities will be:
Moreover, you will be part of a dynamic department and based on your experiences you are expected to be part of other cross functional activities and take ownership and responsibility to drive change and process improvements in the global organisation.
Qualifications
You have:
You take a positive and pragmatic approach to problem solving and you are eager to optimise and simplify processes around you. You are proactive, courageous, and detail-oriented without losing the big picture and quality-conscious as well as curious by nature. You are a great team player, and you thrive working across departments in an international organisation.
Working at Novo Nordisk
To work for Novo Nordisk, you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange we offer you to be a part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
Contact
For futher informations please contact Mona Khan on +4530795496 or [email protected].
Deadline
18 January 2023. We will be screening and interviewing on an ongoing basis.
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
The open position is in Quality Management System (QMS) Operations department in R&D Quality, located in Søborg. In QMS Operations we are responsible for our QMS, we provide Quality support and assurance to our stakeholders.
We are also responsible for coordinating Quality Management Review (QMR) at senior management levels in order to get an overview of the current quality performance, ensure adequacy of the QMS, and ensure quality performance going forward.
Research and Development (R&D) Quality is part of Development organisation and we play a vital role in supporting the drug and device development process to ensure high quality as well as fit-for-purpose processes. In Novo Nordisk, we have an ambitious drug and device development program and we work in a global setting with focus on delivering viable products that make a difference to patients and ultimately benefit society.
The position
The main responsibilities will be:
- Planning and executing QMR. Contribute to the QMR process by calling for, collecting, consolidating and reviewing all relevant input/data from stakeholders in Development and Research & Early Development
- Preparing draft presentation for the QMR meetings including analysis of data by the Tableau QMR data solution. Support, participate and ensure QMR meeting minutes are written
- Handling and approve the deviations from our Quality Management System (QMS) mainly within clinical processes. Facilitate solid actions are defined
- To be part of the Corporate process group for Deviation process chaired by NN Quality and strive for the most optimal process for the clinical deviations and continuous improvement
- Providing training and quality advice to stakeholders globally
Moreover, you will be part of a dynamic department and based on your experiences you are expected to be part of other cross functional activities and take ownership and responsibility to drive change and process improvements in the global organisation.
Qualifications
You have:
- An academic degree in pharmacy, medicine, science or similar
- Experience within quality processes, e.g deviations & CAPA
- Preferably good knowledge of GCP, MDR and other relevant regulations
- Ability to communicate to senior management as well as a broad number of internal stakeholders at all levels
- Excellent interpersonal and collaborative skills with strong communication and presentation skills in both written and spoken English is a prerequisite
- Excellent planning and coordination skills a necessity in relation to QMR
You take a positive and pragmatic approach to problem solving and you are eager to optimise and simplify processes around you. You are proactive, courageous, and detail-oriented without losing the big picture and quality-conscious as well as curious by nature. You are a great team player, and you thrive working across departments in an international organisation.
Working at Novo Nordisk
To work for Novo Nordisk, you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange we offer you to be a part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
Contact
For futher informations please contact Mona Khan on +4530795496 or [email protected].
Deadline
18 January 2023. We will be screening and interviewing on an ongoing basis.
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 Søborg.
Jobbet er oprettet på vores service den 23.12.2022, 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
- Søborg
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