QC Equipment Chemist
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Bagsværd
Would you like to work with complex problem solving, optimization and collaboration in an ambitious Good Manufacturing Practice (GMP) Environment? Do you love metrology, qualification, and maintenance of analytical equipment and wish to upgrade our laboratory with automated procedures and tools for the future? If so, then you could be our new QC Equipment Chemist in our microbiological quality control department located in Bagsværd.
The position
You will be part of a group of equipment responsible chemists and technicians with the overall responsibility of securing compliance so that the department equipment sees minimum down-time. Our equipment consists primarily of isolators, autoclaves, Matrix Assisted Laser Desorption/Ionization-Time-of-Flight (MALDI-TOF), LAL readers, utensil washers, incubators, microscopes, pH-meter, balances, pipettes, refrigerators, freezers, temperature monitoring system (FMS), etc. Your primary tasks will include: High-quality support to analytical teams, ensuring they can conduct the analysis necessary to release our finished products in due time. Approval of the required documentation of both planned and unplanned maintenance of analytical equipment. Setting and maintaining calibration requirements, handling deviations, change requests, and qualification approvals. Contribute to ongoing optimisation of our existing processes with being curious about how other teams and departments operate, both inside and outside of Novo Nordisk. In Novo Nordisk we are on a journey of digitalizing our QC laboratories by e.g., introducing automated processes and connecting laboratory equipment to Laboratory Information Management System (LIMS) to support a paperless future. You will have the opportunity to contribute to this journey by being observant about new, innovative solutions and secure successful implementation.
Qualifications
Your experiences include: An academic degree in Sciences, Engineering, Biotechnology, Pharma or similar, preferably with 3+ years of relevant experience from the pharmaceutical industry or other highly regulated industries. Knowledgeable about the criteria for maintaining analytical equipment and GMP equipment qualification. Setting and maintaining calibration criteria while working with metrology is advantageous, as well as change request, deviation, and technical writing experience. Strong command of English and Danish, as many instructions and documentations are written in Danish.
As a professional, you embrace new ideas and changes and are not afraid to take lead in bringing new solutions, processes, and improvements forward. You are a strong communicator and find it natural to establish new relationships across teams and departments. Finally, you have a quality mindset and a sharp eye for detail. About the department
The QC Microbiology is a department in Injectable Finished Products (IFP) Manufacturing Development and consist of approx. 60 employees organized in 4 teams. The department is responsible for a wide variety of microbiological analysis on Injectable Finished Products, covering release, ID, sterility, and validation samples. We are receiving samples from our world-wide production sites.
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
For further information please contact Jens Kruse, Senior Manager at +4530758644. Deadline
28 June 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.
The position
You will be part of a group of equipment responsible chemists and technicians with the overall responsibility of securing compliance so that the department equipment sees minimum down-time. Our equipment consists primarily of isolators, autoclaves, Matrix Assisted Laser Desorption/Ionization-Time-of-Flight (MALDI-TOF), LAL readers, utensil washers, incubators, microscopes, pH-meter, balances, pipettes, refrigerators, freezers, temperature monitoring system (FMS), etc. Your primary tasks will include:
Qualifications
Your experiences include:
As a professional, you embrace new ideas and changes and are not afraid to take lead in bringing new solutions, processes, and improvements forward. You are a strong communicator and find it natural to establish new relationships across teams and departments. Finally, you have a quality mindset and a sharp eye for detail. About the department
The QC Microbiology is a department in Injectable Finished Products (IFP) Manufacturing Development and consist of approx. 60 employees organized in 4 teams. The department is responsible for a wide variety of microbiological analysis on Injectable Finished Products, covering release, ID, sterility, and validation samples. We are receiving samples from our world-wide production sites.
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
For further information please contact Jens Kruse, Senior Manager at +4530758644. Deadline
28 June 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 9.6.2023, 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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