Quality Assurance Professional
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Søborg
Do you dream of using your great quality mindset in a highly professional and engaged global environment? Do you have excellent collaboration skills and are you up for learning and working in one of the most exciting, dynamic, and complex areas in Novo Nordisk? If so, this position could be a unique opportunity for you to become our new colleague in Research & Development (R&D) - Good Laboratory Practice (GLP) Quality Assurance (QA) based in Søborg, Denmark. Apply now! The position We are looking for a new colleague to help us ensure GLP for non-clinical studies and compliance in clinical laboratories in both Denmark and the United States. We offer you an exciting, challenging, and important role where you become part of a skilled team that acts as quality sparring partners for our stakeholders. You will get great opportunities for both personal and professional development, with growing responsibility depending on your skills and interests. As a QA Professional in GLP Quality , your main task will be to: Ensure quality oversight/compliance verification of GLP at internal GLP studies, external Contract Research Organisations (CROs) , and clinical laboratory studies in Denmark and United States Conduct assessments of new non-clinical and clinical laboratories; monitor and review computerized systems used in Novo Nordisk GLP-regulated laboratories conducting GLP and GCP activities Ensure compliance support to our stakeholders Participate in ad-hoc tasks and projects in the department and participate in inspections by regulatory authorities Some travel activities are expected, approximately 20-30 days of travel days Qualifications
We are looking for someone that can set the right and balanced quality standards within GLP. For this position, we are open to evaluate more senior candidates that will be offered a Senior Quality Assurance role. To be successful in this position, you need to: Hold a master’s degree, in science, pharmacy, medicine, or similar Have experience preferably within GLP, quality assurance, non-clinical research, or industrial drug development Have good analytical skills, are systematic and independent Be fluent in English, both written and spoken As a person, you are self-driven, positive, and a team player. You are curious and thrive in a dynamic environment where collaboration and communication with many different stakeholders will be crucial for your success. You have strong communication, interpersonal skills, enjoy working across departments and in an international setting. About the department GLP QA is a department in R&D Quality which is part of Development in Novo Nordisk. We play a vital role in supporting non-clinical and clinical laboratory research activities. We work together with key stakeholders to ensure compliance. We are expanding our area to include support to our newly established Boston Global Development site in the United States. The Boston Global Development are conducting clinical development programmes and programmes based on advanced technologies. The site is uniquely positioned to draw upon greater Boston's innovative life sciences ecosystem. You will become part of a department with many interfaces in the organization, both in Denmark, United States, and with all our external CRO. The department consists of eight highly knowledgeable and skilled persons, covering the diverse area of GLP within the non-clinical studies and clinical laboratories. 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 to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. Contact For further information, please contact Department Manager, Ditte Vestergaard at +45 34481311. Deadline The deadline for applying is 26 March 2023. To ensure an efficient and fair recruitment process, please refrain from adding a photo to your CV. 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.
We are looking for someone that can set the right and balanced quality standards within GLP. For this position, we are open to evaluate more senior candidates that will be offered a Senior Quality Assurance role. To be successful in this position, you need to:
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 to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. Contact For further information, please contact Department Manager, Ditte Vestergaard at +45 34481311. Deadline The deadline for applying is 26 March 2023. To ensure an efficient and fair recruitment process, please refrain from adding a photo to your CV. 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.
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 9.2.2023, 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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