Supporter for the Microbiological QC
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Are you a passionate and experienced academic looking for a rewarding career in the pharmaceutical industry? Do you have a keen eye for continuous improvement, collaboration, and process optimization? If so, then you might just be the next Supporter for the Microbiological QC to join our great team in Bagsværd! The position
As a Supporter for the Microbiological QC, you will be a part of our Analysis Process Team that is responsible for Environmental Monitoring (EM), Identification of Microorganisms (ID), analysis of Bio Indicator (BI) and Aseptic Process Simulation (APS). The team consists of 22 laboratory technicians and 3 supporters.
Once you join the team you will have a key role in ensuring that our methods and processes are compliant with Good Manufacturing Practice (GMP) requirements, and that our laboratory technicians are well-equipped and trained to conduct analyses. Your primary tasks will include: • Driving and contributing to optimisation of our processes and analytical methods
• Leading systematic improvements by utilization of LEAN principles and tools
• Ensuring compliance with GMP through Deviation Handling, Change Requests, Laboratory Investigations, Standard Operating Procedure (SOP)
• Close collaboration with other Supporters, QA, and laboratory technicians
• Participating in audits and inspections Moreover, you will be driving ongoing process optimization and leading systematic problem-solving initiatives contributing to the ongoing success of our team. You will get the opportunity to explore how other teams and departments function, both within and outside of Novo Nordisk and share gained knowledge with the Analysis Process Team. Qualifications
We are looking for someone who understands the complexity of working in the pharmaceutical field. Our ideal candidate can easily process data and is eager to learn and contribute to producing the finest solutions. Your experience includes: • MSc in Natural Sciences, Microbiology, Pharmacy or Engineering, with at least 3 years of experience from a supporting function in the pharmaceutical industry
• Knowledge of GMP, microbiology and LEAN
• Experience with EM, ID and BI analysis methods will be considered an advantage
• Expertise working as a Supporter in aseptic production or laboratory will be viewed as advantageous
• Professional proficiency in both English and Danish On a personal level, you are self-motivated and not afraid to take initiative and new responsibilities. You are a great communicator and enjoy establishing new relationships with colleagues. You are known for your good collaboration skills, and you comply with deadlines and possess a systematic approach to problem-solving. 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. 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 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
08 December 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.
As a Supporter for the Microbiological QC, you will be a part of our Analysis Process Team that is responsible for Environmental Monitoring (EM), Identification of Microorganisms (ID), analysis of Bio Indicator (BI) and Aseptic Process Simulation (APS). The team consists of 22 laboratory technicians and 3 supporters.
Once you join the team you will have a key role in ensuring that our methods and processes are compliant with Good Manufacturing Practice (GMP) requirements, and that our laboratory technicians are well-equipped and trained to conduct analyses. Your primary tasks will include: • Driving and contributing to optimisation of our processes and analytical methods
• Leading systematic improvements by utilization of LEAN principles and tools
• Ensuring compliance with GMP through Deviation Handling, Change Requests, Laboratory Investigations, Standard Operating Procedure (SOP)
• Close collaboration with other Supporters, QA, and laboratory technicians
• Participating in audits and inspections Moreover, you will be driving ongoing process optimization and leading systematic problem-solving initiatives contributing to the ongoing success of our team. You will get the opportunity to explore how other teams and departments function, both within and outside of Novo Nordisk and share gained knowledge with the Analysis Process Team. Qualifications
We are looking for someone who understands the complexity of working in the pharmaceutical field. Our ideal candidate can easily process data and is eager to learn and contribute to producing the finest solutions. Your experience includes: • MSc in Natural Sciences, Microbiology, Pharmacy or Engineering, with at least 3 years of experience from a supporting function in the pharmaceutical industry
• Knowledge of GMP, microbiology and LEAN
• Experience with EM, ID and BI analysis methods will be considered an advantage
• Expertise working as a Supporter in aseptic production or laboratory will be viewed as advantageous
• Professional proficiency in both English and Danish On a personal level, you are self-motivated and not afraid to take initiative and new responsibilities. You are a great communicator and enjoy establishing new relationships with colleagues. You are known for your good collaboration skills, and you comply with deadlines and possess a systematic approach to problem-solving. 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. 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 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
08 December 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 17.11.2023, 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.
- Øvrige
- Bagsværd
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