Solvias is a world leader in contract research, development and manufacturing. The industries we serve include pharmaceuticals, biotech, medical devices and cosmetics. With our excellent infrastructure and unrivalled expertise, we develop, analyze and test a wide range of biological and chemical substances and products.Would you like to be a team member in the Business Unit Biopharma? We're looking for a dynamic professional personality as ReviewerJob Description
Review of raw data in the department of Small Molecules with focus on GC and HPLC methods (validation, development and routine orders)
Preparation and review of validation protocols and reports
Clarification of OOS, processing of deviations
Contributing to the continuous improvement of quality and the optimization of processes
Support knowledge transfer and employee training as part of the continuous improvement of our services
Requirements
Profound (several years) experience in the GMP regulated environment and a view of the overall context
Experience in the documentation and review of raw data
Expert in the application of chromatography data systems (ideally Chromeleon)
In-depth knowledge in the field of GC and HPLC method validation (ideally experience with statistical methods)
Ideally experience in QC analysis of chromatographic methods
Experience with LIMS desirable
Very good knowledge of Excel
Team-oriented and communicative personality
Very good knowledge of German and English
We offerWe offer attractive compensation packages and flexible work schedules. At Solvias we believe that every individual matters and can make an impact. Our employees are able to grow professionally and to evolve as people. We look forward to receiving your complete application documents.
If you have any questions, please contact: Ms. Regula Degen Email: regula.degen@solvias.comApply now
