Research Scientist, Formulation and Quality Cont

Camurus provides innovative nanoscale drug delivery systems for the development of new and improved pharmaceuticals.Our advanced solutions range from long-acting injections to lipid nanocarriers designed for intravenous, transdermal and oral delivery.These are used in own drug development programs as well as in partnership with pharmaceutical and biotechnology companies worldwide. Headquartered at Ideon Science Park in Lund, Sweden, in the heart of Medicon Valley, Camurus maintains close ties with academic institutions, contract research organizations and pharmaceutical companies around the globe. We are looking to strengthen the organization with a Research Scientist: Formulation and Quality Control Job summary: Camurus is seeking a qualified and highly motivated formulation scientist with quality assurance responsibilities to work in our Pharmaceutical Development group in the research and development of new pharmaceutical products.The work is performed in in-house projects as well as in collaboration projects with partners.The work involves laboratory experiments, physico-chemical characterization of formulations, documentation of results, batch documentation and manufacturing for e.g.preclinical testing.Other assignments specifically relate to quality assurance responsibilities such as instrument responsibilities, development and review of SOPs and Methods, quality control of batch documentation, responsibility for chemicals and materials supply and coordination of stability programs and compilation of stability reports. We want you to have: A B.Sc.in chemistry/pharmacy, Biomedical Analyst, or similar university degree or at least 5 years professional experience within pharmaceutical R&D Broad experience of laboratory work, preferably within the pharmaceutical sector and with experience of quality assurance responsibilities Willingness to work in a fast-paced, dynamic and team-oriented environment Ability to perform challenging tasks independently or in collaboration with colleagues Good experience in writing reports and using Ms Office programs Excellent communication skills in English Positive attitude to new challenges It is considered as an advantage if you have experience of working in a GMP/GLP environment and/or have knowledge about regulatory guidelines such as ICH-guidelines.