Professional for Microbiological QC
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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, wanting to ensure our laboratory is compliant with Good Manufacturing Practice (GMP) requirements? If so, you could be our new Professional for Microbiological QC based in Bagsværd. Read on to find out more and apply today to join us for a life-changing career! The position You will be part of the Analysis Process Team where you will be responsible for ensuring high-quality support to the laboratory technicians in the team, securing that they are trained and well-equipped to conduct our analysis, and making sure the method and equipment comply with GMP requirements. Your primary tasks will include: Driving and contributing to ongoing optimization of our existing processes and analytical methods. Handling Deviations, Change Requests, Laboratory Investigations, Standard Operating Procedure (SOP) updates as well as leading systematic problem-solving. Exploring how other teams and departments work, both within and outside Novo Nordisk and bringing new knowledge to the team. Participating in audits and inspections. The Analysis Process Team, which you will be part of, is responsible for Environmental Monitoring (EM), Identification of Microorganisms (ID), analysis of Bio Indicator (BI) and Aseptic Process Simulation (APS). The team consists of 20 laboratory technicians and 3 supporters, where you will become the fourth. Qualifications Your experiences include: You hold an MSc in Natural Sciences, Microbiology, Pharmacy or Engineering, preferably with 5+ years of experience from a QC function in the pharmaceutical industry. Extensive knowledge of GMP, microbiology, and LEAN. Experience with EM, ID, and BI analysis methods will be considered an advantage. Expertise working as a professional in aseptic production will be viewed as a benefit. Professional proficiency in English and Danish (written and oral) is a prerequisite, as many instructions and documentations are written in Danish. As a professional, you are self-motivated and never afraid to take initiative or to take on responsibilities. You are a strong communicator; you find it natural to establish new relationships and are known for your good collaboration skills. It is second nature for you to comply with deadlines, have a systematic approach to problem-solving, and possess a flair for processing data. You are eager to learn and are energized by communicating with your colleagues, together producing the finest solutions. 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 60 employees divided into 4 teams. Our department has the overall responsibility for the microbiological analysis of finished insulin products and water samples coming from production. 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 analyses, Total Organic Carbon (TOC) and Chemical Water (CW). Our daily operations involve close dialogues with our closest stakeholders in the aseptic manufacturing areas, other QC laboratories, and Quality Assurance. Working at Novo Nordisk 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 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 Vladimir Radivojsa, Associate Manager at +45 34483633. Deadline 20 November 2023. Please note, applications will be reviewed, and interviews will be conducted on an ongoing basis. 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.
Information og data
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 15.6.2023, 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.
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