Quality Assurance Professional
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Søborg
Are you passionate about quality and simplicity, and get motivated by solving issues and finding improvement solutions? Do you want to work closely with colleagues from all over the world in a company that is growing? Then bring your passion and skills and join our diverse & inclusive Quality department as our new QA colleague. The position
We are looking for a new Quality colleague to join our GS & RA Quality department in R&D Quality, located in Søborg. You will become part of a team consisting of 9 members who comes from several different countries.
The position is very versatile, and you get the opportunity to work with stakeholders all over the world.
Your core responsibilities will be to:
Provide quality advice and ensure quality oversight & compliance of Regulatory and Safety processes Review and QA approve Standard Operating Procedures (SOPs) ensuring that the external requirements are reflected Challenge SOP author on unnecessary complexity in process Handle and QA approve deviations, and guide during root cause analysis Handle and QA approve Change Requests - support in assessment of new changes, new requirements Be the Quality advisor and partner in improvement projects securing compliance with GxP regulatory requirements Facilitate workshops, and share knowledge within the department and across R&D Quality
You will be part of a dynamic area with many transformation initiatives, where you will participate in setting the right quality bar in the global organisation. Qualifications:
In this role we expect you to have an academic degree, e.g. a master’s degree, within Pharmacy, Engineering, Data Science, Natural science, Economics, Computer Science, among others.
Furthermore:
A strong command of written and spoken English Relevant experience/knowledge within quality, quality processes, or GxP knowledge Analytical skills and experience with analytical tools Experience with facilitating workshops, and presenting your work Experience producing clearly written documentation Business understanding and cross-organisational experience
As a person: You like to work independently and to take initiative Curious and interested in learning new things Structured, and self-driven You contribute to good collaboration Able communicate complex information in a simple way
We value a candidate with an eye for details, yet at the same time being able to set things in perspective and see the big picture. The perfect candidate will be known for their high-quality work, positive attitude, and ability to quickly obtain an overview of a given subject. About the department
R&D Quality is part of the Development organisation and plays a vital role in supporting the drug and device development process to ensure high quality as well as fit-for-purpose processes throughout the entire value chain. The open position is in the GS & RA Quality. This Quality department is responsible for Quality support and Quality Management System activities across all processes in Global Safety (GS) and Regulatory Affairs (RA) areas via global stakeholder interaction. The department consists of QAs for deviations, SOPs (standard operating procedures), change controls, quality monitoring, process reviews, and we are quality partners in transformational projects.
We work in a global setting with focus on delivering viable products that make a difference to patients and ultimately benefit society. We are busy and are on an exciting journey bringing quality on top of the agenda throughout the R&D organisation – and maybe you are the one to join us on this journey. Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambition help us change lives for the better for patients around the world. As their needs evolve, so does our challenge to find better and more innovative ways to improve their quality of life. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development. Contact For further information, please contact Lavinia G. M. Pedersen +45 30799636
Deadline:
The 4th of June 2023. We will review applications and conduct interviews on an ongoing basis. 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. 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.
We are looking for a new Quality colleague to join our GS & RA Quality department in R&D Quality, located in Søborg. You will become part of a team consisting of 9 members who comes from several different countries.
The position is very versatile, and you get the opportunity to work with stakeholders all over the world.
Your core responsibilities will be to:
In this role we expect you to have an academic degree, e.g. a master’s degree, within Pharmacy, Engineering, Data Science, Natural science, Economics, Computer Science, among others.
Furthermore:
A strong command of written and spoken English
R&D Quality is part of the Development organisation and plays a vital role in supporting the drug and device development process to ensure high quality as well as fit-for-purpose processes throughout the entire value chain. The open position is in the GS & RA Quality. This Quality department is responsible for Quality support and Quality Management System activities across all processes in Global Safety (GS) and Regulatory Affairs (RA) areas via global stakeholder interaction. The department consists of QAs for deviations, SOPs (standard operating procedures), change controls, quality monitoring, process reviews, and we are quality partners in transformational projects.
We work in a global setting with focus on delivering viable products that make a difference to patients and ultimately benefit society. We are busy and are on an exciting journey bringing quality on top of the agenda throughout the R&D organisation – and maybe you are the one to join us on this journey. Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambition help us change lives for the better for patients around the world. As their needs evolve, so does our challenge to find better and more innovative ways to improve their quality of life. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development. Contact For further information, please contact Lavinia G. M. Pedersen +45 30799636
Deadline:
The 4th of June 2023. We will review applications and conduct interviews on an ongoing basis. 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. 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 11.5.2023, 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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