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.
Kymos is hiring a Scientist in our Bioanalysis department:
Position Description: We offer a position in the Bioanalysis Department as a Scientist responsible for the analysis of active ingredients and pharmaceutical specialties.
The Job main missions will be:
Design, develop, qualify and validate HPLC-UV analytical methods for compound determination in matrices (sample preparation, method set-up) coming from in vitro percutaneous absorption projects.Ensure coordination and good performance of laboratory technicians.Manage the projects directly with our clients.Knowledge of LC-MS/MS technique will be valuable.The work is conducted in compliance with GLP and GMP regulations.
Education: Bachelor's degree in Chemical Sciences (Analytical Orientation) with specialization in HPLC-UV.
A Ph.D. is highly valued.
Skills and experience: Service oriented mindset to deliver on time and with the appropriate level of quality, to research projects expectations/needs.
High experience in HPLC-UV techniques and basic knowledge of LC-MS/MS methods.
Anticipate issues and proactively identify workaround options, showing strong "results" orientation.
Work closely and interact constantly with technicians and clients.
Fluent in speaking, reading and writing professional English.
3/4 years' experience as Senior Scientist in a pharmaceutical environment and under GLP/GMP regulations.
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