- The design, supervision and execution of the quality control studies of Biological Products.
- The design, supervision and execution of quality control studies including chromatography and HPLC . At least 3 years of experience with these techniques are required.
- The management of the assigned projects keeping the deadlines and establishing a direct communication with the client
- Technical document writing associated with the studies (protocols, reports, standard procedures, certificates of analysis, etc.)
- The direction and supervision of the experimental work of the technical staff in charge.
- The knowlegde of electrophoretic techniques, Western-Blot and ELISAs will be a plus.
- Degree in Biochemistry, Biotechnology, Chemistry or related
- Experience in HPLC methods, Quality Control of Proteins will be a plus.
- Good command of English
- Experience in working in GMP environments is a must.
- Availability to work a year around to cover maternity leave.
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Scientist Biopharma - España - Kymos Group
Descripción
We are an innovative and fast-growing CRO offering you the opportunity to develop your career in an excellent working environment. Kymos Group is a scientific-technical services company directed to companies of the chemical-pharmaceutical and veterinary sector.
KYMOS offers a wide range of analytical services in Medicinal Chemistry to optimize the research, the development and the quality control for innovative, generic and biological drug substances and drug products from the preclinical stage to market.
KYMOS also has an extensive experience in developing and validating bioanalytical methods and sample analysis in any biological matrix using the latest technology. Mass spectrometry and immunology laboratories are available to carry out small molecule and biologic projects.
KYMOS is also an international group, Kymos Group, with sites in Italy, PHARMAPROGRESS and in Germany, PROLYTIC.
We are looking for a Scientist for our Biopharma department.
Under the supervision of the Department Manager, the Scientist will be responsible for the following duties:
Requirements
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