Academic Supporter for Microbiological QC laboratory

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Bagsværd

Are you passionate and experienced working with QC laboratory processes and applied microbiology? Are you dedicated to collaboration and high quality, and want to ensure our laboratory is compliant with GMP requirements? Then you may be our new colleague! About the department Injectable Finished Products (IFP) Quality Control (QC) Microbiology is part of IFP Manufacturing Development. The department is located in Bagsværd and consists of 50 employees divided into 4 teams. Our department has the overall responsibility for the microbiological analysis of finished insulin products and water samples coming from the productions. Analysis performed in the department includes environmental monitoring (EM), Test For Sterility (TFS), Bacterial Endotoxin Testing (LAL), Total Viable Count (TVC) and High Voltage Leak Detection (HVLD). Recently we have insourced two chemical analysis, Total Organic Carbon (TOC) and Chemical Water (CW). Our daily operations involve a close dialogue with our nearest stakeholders in the aseptic manufacturing areas, other QC laboratories and Quality Assurance. The position You will be part of the Analysis Process Team where you will be responsible for ensuring a high-quality support to the laboratory technicians in the team, ensuring that they are trained and well-equipped to conduct our analysis and ensuring that the method and equipment comply with GMP requirements. The Analysis Process Team which you will be part of are responsible for environmental monitoring (EM), identification of microorganisms, analysis of Bio indicator and Total Organic Carbon (TOC). The team consists of 18 laboratory technicians and 3 supporters, where you will be the fourth. All so we must ensure release of our finished products in due time to continue the steady supply of medicines to our patients. This includes handling of Deviations, Change Requests, Laboratory Investigations, SOP updates as well as leading systematic problem solving and participating in audits and inspections. Moreover, you will be expected to contribute to ongoing optimisation of our existing analytical methods. This also entails being curious about how other teams and departments work, both within and outside Novo Nordisk and bringing new knowledge to the team. Qualifications You hold a MSc in Natural Sciences, Microbiology, Pharmacy or Engineering, preferably with 2+ years of experience from a QC function in the pharmaceutical industry. You are strong in GMP, microbiology and LEAN. Moreover, experience with some of the mentioned analysis will be considered an advantage. If you have experience from a position as an academic in aseptic production you might also be an interesting candidate. Professional proficiency English (written and oral) and Danish (written and oral) is a prerequisite. As a person, you are self-motivated and never afraid to take initiative or to take on responsibilities. You are a strong communicator, and you find it natural to establish new relationships and you are known for your good collaboration skills. It is also natural for you to comply with deadlines, have a systematic approach to problem solving and flair for processing data. You are curious to understand and gain energy by interacting with your colleagues and together finding the best solutions. Working at Novo Nordisk At Novo Nordisk we recognise 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 the communities we operate in. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. We are happy to discuss flexible working, depending on the role and subject to business needs. Contact For further information please contact Associate Manager Vladimir Radivojsa at +45 34483633. Deadline 10th of April 2023 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 Bagsværd.

Jobbet er oprettet på vores service den 13.12.2022, men kan have været deaktiveret og genaktiveret igen.

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