Senior Aseptic Manufacturing Professional

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Gentofte

Are you motivated by the pulse in a production & project department? Do you want to be part of a strong team with high professionalism and challenging processes? Would you like to be a part of the project group responsible for implementing and qualifying our new isolator filling line in Biotech and Rare Disease (BRD) located at building HAC in Gentofte?
If yes, you could be one of the two new Senior Aseptic Manufacturing Professionals we are looking for. Apply today and join us!
The position
As Senior Aseptic Manufacturing Professional you will be a part of the department for Isolator Filling. The department is responsible for aseptic filling of biopharmaceutical products within the rare blood disorders and obesity areas using isolator technology.
You will be a part of the project HAC Future Fill, which is responsible for implementing two new Isolator filling lines in Gentofte.
Your main responsibilities will be focused on:
• Risk assessments within use of polymers and Single Use Systems
• Being responsible for preparing and executing various qualification and test activities e.g., VHP cycle validation, smoke studies, Process Characterization, Process Validation, and Aseptic Process Simulation, etc
• Driving the connection between qualification knowledge and -results to how our process flows are described
As many tasks are new, the design and description of the processes will be executed in close collaboration with fellow project members, specialists, pharma consultants, and our vendor of the isolator filling line. It is expected that you will take the lead of your own area of responsibility.

Qualifications
As the ideal candidate, you should have:
• An academic degree within natural science, which could be a master’s degree related to Pharmacy, Microbiology or other relevant areas
• At least, 6 years of experience in working with qualification activities in a production facility
• A profound knowledge of aseptic isolator filling is highly valued
• Experience with working in a highly regulated environment according to cGMP
• Full professional proficiency in English and Danish is expected
As a person you have a positive can-do approach to challenges, which you investigate through curiosity in close collaboration with your team. You perform your investigation in a structured way without losing focus on the importance of maintaining high quality throughout your work. About the department
Finished Products site Gentofte and Værløse is part of Biotech & Rare Disease (BRD). At our sites in Gentofte and Kirke Værløse, we are more than 750 colleagues responsible for transforming the API (Active Pharmaceutical Ingredient) into the finished products for people living with serious chronic diseases. We work with advanced processes such as formulation, filling, freeze-drying in a sterile environment, assembly, and packaging. We bring value to our patients by delivering high-quality products in accordance with Good Manufacturing Practice (GMP) in a timely and cost-effective manner as we constantly optimise our processes and invest in the latest technology. Working at BRD, Novo Nordisk
BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD, we are not only supplying Novo Nordisk products to people living with serious chronic diseases, but we also use our competences in biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk.
We are more than 3000 dedicated colleagues working at six production sites in Denmark and the United States. Here we cover the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. As more and more people need our products, we support Novo Nordisk's initiatives in new therapy areas. Every day, we work to streamline and expand our capacity through process innovation, automation, and the introduction of new technology.
Contact
For further information, please contact Associate Manager Henning Hansen at +45 30 79 63 21.

Deadline
25 February 2024
Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible.
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 Gentofte.

Jobbet er oprettet på vores service den 20.12.2023, 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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