Join Xellia in Copenhagen as Scientist / Senior Scientist

apartmentXellia Pharmaceuticals ApS placeKøbenhavn calendar_month 
We are looking for a new colleague to join the Analytical Development Laboratory, in the R&D Department of Xellia Pharmaceuticals ApS, to contribute to the crucial process development for the manufacture of life-saving antibiotics. We are looking for a Scientist/Senior Scientist to strengthen our team.
Xellia R&D is organized in different departments located in Oslo, Copenhagen, and Budapest with a total of about 50 employees. Currently, we have a vacant position in the Analytical Development Laboratory in Copenhagen. Your new team Analytical Development Laboratory is responsible for development and validation of analytical methods.
The department utilizes a variety of analytical techniques including TGA/DSC, HPLC/UHPLC, LC-MS/MS, 2D-LC-MS and GC-FID. Additionally, the department performs characterization of isolated impurities in connection with production and registration of existing and new Active Pharmaceutical Ingredients (APIs).
As a team member in Analytical Development Laboratory, you will have the responsibility for the analytical methods for our products and will be working closely with a highly skilled team of Scientists and technical personnel located in R&D, production, QC-labs and Regulatory Affairs.
Room for development and responsibility At Xellia, every single colleague counts. As a small company, we are good at making room for the individual. If you seek out development, knowledge or more responsibility, you will rarely get no, and it gives you the opportunity to dive into your area.
Because we know that the belief in talent combined with the desire to grow is the recipe for growth. Both for you and for us. Your role and responsibilities Develop, validate, and transfer HPLC/UHPLC and GC methods for new and existing products.
Design, plan, and evaluate experiments in collaboration with scientists and technicians. Evaluate, document, and report data in compliance with GMP. Investigate and characterize impurities in products. Contribute to analytical control packages covering release, stability, and in-process monitoring.
Support Regulatory Affairs and Quality during inspections and product filings. Profile and Skills M.Sc. or Ph.D. in Analytical Chemistry with relevant industry experience (biotech/pharma preferred). Strong expertise in HPLC/UHPLC, GC, and analytical method development/validation.
Experience with LC-MS, NMR, spectroscopic, and standard analytical techniques. Knowledge of Pharmacopeias, regulatory guidelines, and GMP framework. Strong collaboration skills and passion for laboratory work. Are we your new colleagues? At Xellia, you’ll join a collaborative and friendly team in a stable, international company with a strong purpose.
We offer a dynamic, multinational working environment where you’ll have the opportunity to learn, grow, and make a meaningful impact. Please apply with your application no later than September 30. We will be reviewing applications and interviewing candidates on an ongoing basis, so we encourage you to apply as soon as possible.
If you have any questions, please reach out to Senior Manager R&D Jon Efskind, jon.efskind@xellia.com, mob: +47 4840 2267, or Associate Manager Jacob Krall, jacob.krall@xellia.com, +45 4193 3773. We look forward to hearing from you. Xellia Pharmaceuticals is a specialty pharmaceutical company and a global leader in providing anti-infective treatments and other critical care therapies for serious and often life-threatening conditions.
Xellia has an extensive heritage in developing, manufacturing, and commercializing anti-infective products. Headquartered in Copenhagen, Denmark, and owned by Novo Holdings A/S, Xellia Pharmaceuticals has more than 1400 employees globally, including state-of-the-art manufacturing sites in China, Denmark, and Hungary.

Our strong market position is built on more than 120 years of pharmaceutical industry experience. Further information about Xellia can be found at: www.xellia.com Connect with us on LinkedIn Apply Læs mere 104 evalueringer på Jobindex 4 af 5 stjerner Ansættelsestype: Permanent Ugentlig arbejdstid: Full-time

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