Quality Assurance Professional - Laboratory QA

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Hillerød

Are you motivated by regulatory requirements, setting compliance direction and advice your colleagues across the organization? Are you a solution-oriented person with a passion for Quality Assurance? Do you get inspired by using quality as an active driver of securing Device and Primary Packaging products during development are tested in a compliant environment? If yes, then you might be the person we are looking for in Devices & Delivery Solutions Quality in Hillerød, Denmark. Apply now for our Quality Assurance Professional job opportunity focused on Quality Oversight of Verification Laboratories.
The position In this position, we are looking for a candidate to provide quality oversight of test method, equipment, and laboratories for verification of Medical Device, Primary packaging and Drug Device Combination Products in the development portfolio of Devices & Delivery Solutions in Novo Nordisk. As Quality Assurance Professional, you play a very important role where you work with many different stakeholders both internally in Novo Nordisk, and with outsourced test partners. You will be responsible for setting the compliance direction within operations in laboratories as well as testing equipment, methods, and IT in digitalised and automated laboratory processes. Core responsibilities include:
  • Quality oversight of the laboratory processes.
  • Handling most situations independently, apply your subject matter knowledge and identify better practice and drive improvements to Quality Assurance processes.
  • QA on procedures and instructions related to the laboratory.
  • QA on validation of Test Methods, IT systems, Computerized Equipment and Measurement Equipment.
  • Playing an active role in sharing knowledge and learnings and thereby letting your colleagues learn and shine.
    • Qualifications To fulfil the role, you have:
  • Hold a master’s degree within engineering, Medicine and technology, pharmacy, chemistry or similar with a strong quality mindset.
  • Have experience from laboratory or QA activities, within the Pharmaceutical or Medical Device industry .
  • Fluent in both written and spoken English at a professional level.
    • In addition, some of your strengths include constructively engaging with stakeholders and navigating cross-organisational stakeholder landscapes. You have ability to quickly understand situations and dilemmas and are solution oriented in introducing innovation within procedural and regulatory constraints along with translating regulatory guidance into operational practice to support and guide our laboratories. Clear communication and use of facts to present your point of view when needed to ensure regulatory compliance or patient safety is highly required, as well as being able to notice when our processes can be improved and have the drive to make change happen. About the department Devices & Delivery Solutions Quality is accountable for covering all quality aspects in the development portfolio of primary packaging, mechanical devices, devices with embedded electronics and software, and software as a medical device, as well as projects investigating new paradigms for drug delivery. Further, we work on Quality Management System activities, quality oversight of our suppliers, and host inspections. We are an international team of 30 passionate Quality Assurance experts with diverse backgrounds of which the vast majority is based in Hillerød, Denmark - and a small part of the Device R&D located in USA. Along with the rest of the device development area, we have a high focus on patients and take pride in having a significant impact on the life of patients by ensuring high quality, safe, and effective products. 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 If you have any questions about the job, please do not hesitate to call Dean Kloe, Quality Senior Manager at +45 3075 8948. Deadline 14 January 2024. 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.


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    Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

    Arbejdsstedet er beliggende i Hillerød.

    Jobbet er oprettet på vores service den 21.12.2023, men kan have været deaktiveret og genaktiveret igen.

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