Join Xellia in Copenhagen as Scientist / Senior Scientist
Join Xellia in Copenhagen as Scientist / Senior Scientist
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1 Vacancy
Job Description
R&D
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
- . 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 youll join a collaborative and friendly team in a stable international company with a strong purpose. We offer a dynamic multinational working environment where youll 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 mob: or Associate Manager Jacob Krall 45 .
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 history in developing manufacturing and commercializing anti-infective products including Active Pharmaceutical Ingredients (APIs) as well as Finished Dosage Forms where the majority are injectable drug products.
Headquartered in Copenhagen Denmark Xellia has a global footprint with R&D manufacturing and commercial operations across Europe Asia the Middle East and North America. Xellia Pharmaceuticals is wholly owned by Novo Holdings A/S and employs a dedicated team of more than 1200 people.
Further information about Xellia can be found at:
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Required Experience:
Senior IC
Employment Type
Full-Time
