Research Scientist/Senior Scientist in Analytical Chemistry

We are looking for a new colleague that will contribute to our further success within analytical chemistry. Analytical Development department is responsible for development and validation of analytical methods. We perform isolation and characterization of impurities in connection to production and registration of existing and new Active Pharmaceutical Ingredients (APIs). We are 13 people in Analytical Development; one leader, six research scientists, two engineers and four laboratory technicians. The department is divided on two sites in Oslo and Copenhagen. The location for this position will be in either Oslo or in Copenhagen.

Working tasks:

Together with your colleagues your responsibilities will be:

·         Development and validation of HPLC/UHPLC- and GC-methods for both existing and new products.

·         Design/evaluate experiments and report results in cooperation with scientists, engineers and laboratory technicians.

·         Ensure traceability and documentation of results in accordance to GMP.

·         Participate in project work and be responsible for development of the complete package needed for analytical control of the product.

·         Investigate and characterize impurities in existing and new products.

·         Ensure tech transfer of the analytical procedures, which will require some abroad travelling.

·         Give support to Regulatory Affairs and Quality functions during inspections and in connection with product filings etc.

Our candidate:

·         Has a M.Sc. or Ph.D. in analytical chemistry and 2-5 years of experience from biotech/pharmaceutical industry or other relevant experience.

·         Is strong in method development in HPLC/UHPLC and GC.

·         Has good knowledge in validation of analytical methods.

·         Can work with LC-MS and spectroscopic techniques.

·         Has a wide experience in standard analytical techniques.

·         Has a good knowledge of Pharmacopeias and relevant Guidelines.

·         Has experience of work under the GMP regulatory framework.

·         Is fluent in English and preferable Norwegian/Danish.

·         Is a strong collaborator and has experience of project work.

·         Knowledge of using and interpreting data from NMR and/or NIR is appreciated.

Apply for the position using the following link (only  apply using this link):

https://career5.successfactors.eu/career?company=xelliapharma&career_ns=job_listing&navBarLevel=JOB_SEARCH&rcm_site_locale=en_GB&selected_lang=en_GB&career_job_req_id=5018