QC Supporter for Device Laboratory – iAgora Europa – null

Descripción del puesto:Are you our new dedicated Quality Control Supporter with an interest in tests of medical devices? Do you enjoy working with LIMS, Stability Studies and Device tests? And do you want to become part of the important effort to ensure that people living with chronical diseases can always count on Novo Nordisk products to be safe and effective?Then you might be our new colleague in Device Manufacturing Development (DMD) in Hillerød.About the departmentPilot Operations is part of Device Manufacturing Development (DMD), where we test new products before they are introduced to the market. Our work is related to both production and testing of Novo Nordisk’s line of innovative pen dosage systems.You will join a team of 16 laboratory technicians. 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.The positionTogether with your team, you will be responsible for Device Testing and Quality Control processes for new and existing products. You will mainly be working with Device Stability, Device Release tests and Device Verification tests like; dosage accuracy, dose force and tests of mechanical and physical properties of various electronic components and devices. 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 we strive to be ahead of regulative standards and build our position in a growing market.We strive to work paperless in our laboratories, hence LIMS and other digital platforms is a large part of our daily work.You will be sharpening your collaborative and communication skills when you work with colleagues across and beyond a diverse organisation.QualificationsWe expect you to be a laboratory technician/tester or have a similar educational background that has enabled you to build experience within testing of mechanical and electronic devices. You have worked with Good Manufacturing Practice (GMP) processes before and have a solid experience with LIMS, in a regulated laboratory environment.You like to collaborate around exciting challenges, with a sense of urgency and strict quality standards. We expect you to be structured in your work, actively seek out the knowledge you need and work with a high level of responsibility. You can care for details without missing a deadline, and you take pride in the quality of your work.We expect you to be fluent in both Danish and English, both verbally and in writing.We expect you to have a relevant science education, experience in GMP in QC-laboratories, you have strong desire to learn and work with LIMS, in a regulated laboratory environment.You like to collaborate around exciting challenges, with a sense of urgency and strict quality standards. We expect you to be structured in your work, actively seek out the knowledge you need and work with a high level of responsibility. You can care for details without missing a deadline, and you take pride in the quality of your work.We expect you to be fluent in both Danish and English, both verbally and in writing.As QC supporter in Laboratory Operations your task will among other be: * Laboratory Support* Local Test Method responsible* Deviation handling* Laboratory Investigations (LI’s)* Review and verification of test methods (LIMS)* Handling of laboratory procedures and SOP’s.* Drive local improvement projects. Working at Novo NordiskIn Novo Nordisk, you will be met with trust and exciting professional challenges. You will have the opportunity to work with dedicated colleagues, who strive every day to deliver perfection to the many people living with chronical diseases using our devices. We are proud to make a difference and look forward to welcoming you here.You can learn more about working at Novo Nordisk here: http://wxx.xxxxxxxxxxx.xxx/xxxxxxx/xxxxxxx-xx-xxxx-xxxxxxx.xxxlContactShould you have questions about the position, you are welcome to call Tina Povlsen at +xx xxxx xxx9 in week 28+30 and by mail txxx@xxxxxxxxxxx.xxm in week 30-32.Deadline17-Aug-2021.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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