QC Equipment Scientist

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Hillerød

Do you want to develop your experience in quality control (QC) and validation further? Are you interested in working with laboratory equipment qualification for medical devices? Would you thrive in taking on a challenging role in a dynamic and innovative department? Then apply today as you might be the QC Equipment Scientist we are looking for to join our Device Manufacturing Development (DMD) team within Novo Nordisk. The position As QC Equipment Scientist, you will be responsible for validating and qualifying test equipment and overseeing the validation process. Additionally, you will be supporting the development of testing competencies to enhance device development by optimizing existing test and measurement processes. Together with your team, you will oversee the device testing and quality control processes for new and existing products. You will mainly be working with device QC release tests; dosage accuracy, dose force and tests of mechanical and physical properties of various electronic components and devices and device stability. Some of your main tasks include:
  • Equipment and Local Test Method responsible
  • Laboratory Support and Laboratory Investigations (LI’s)
  • Handling of Deviation, laboratory procedures as well as editing department documents, including Standard Operating Procedures (SOPs), validation documentation, and other equipment- and method-related documentation.
  • Taking ownership of equipment-related activities, ensuring compliance and maintenance of measuring equipment
  • Driving local improvement projects and sharing best practices across device-related areas.
    • We work with a range of advanced test equipment, and here you will have the opportunity to build your knowledge about state-of-the art test technology like cobots, as our aim is to be ahead of regulative standards and build our position in a growing market. Sustainably is high up on our agenda, which is why we strive to work paperless in our laboratories, hence LIMS and other digital platforms is a large part of our daily work. Qualifications To be successful in this role, we imagine you:
  • Hold at least a bachelor’s degree within engineering, medicine and technology, pharmacy, chemistry or any other relevant field
  • Possess a previous experience with QC and validation, ideally obtained from laboratory activities and have worked with quality processes
  • Demonstrate excellent cooperation, stakeholder management and organisation skills
  • Are fluent in English, both spoken and written
    • It would be considered as an advantage if you have a previous experience within the pharmaceutical or medical device industry, as well as has experienced with interpretation of relevant regulatory requirements and standards. As a person, you approach your work with an openminded and positive attitude, you thrive in making a difference and are eager to learn. You like to collaborate around exciting challenges, with a sense of urgency and strict quality standards. You are known as someone who can meet deadlines with a structured approach and keep the overview – even in a busy environment where priorities can change quickly. You enjoy working and delivering results independently and at the same time are a team player who shines together with your colleagues. About the department Who is the team waiting for you? Our team QC and Stability Laboratory is part of Device Manufacturing Development (DMD), where we are responsible for QC release test on new products before they are introduced to the market and device stability on Drug Device Combinations products. Your new colleagues will be 7 laboratory technicians and 5 scientists, all excited to welcome and share knowledge with you. We operate in a diverse landscape of stakeholders, balancing many concerns in a complex, international business environment, and we never compromise on the quality of our work. We share an informal tone, great work morale and tall ambitions to be the best at what we do. 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 Should you have questions about the position, you are welcome to call Tina Povlsen at +45 3079 1569 or by email [email protected] Deadline 17 March 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 5.3.2024, men kan have været deaktiveret og genaktiveret igen.

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