Solutia Life Sciences (recruitment division of Solutia) specializes in technical and middle management profiles in the pharmaceutical, biotech, and medical device sectors.
We are currently selecting a Scientist for Biologics Quality Control for a scientific-technical services company serving businesses in the chemical-pharmaceutical and veterinary sectors, located in Cerdanyola del Vallés.
The Scientist will be responsible for the following duties:
* The design, supervision and execution of quality control studies of Biological Products including chromatography and HPLC. At least 3 years of experience with these techniques is required.
* The management of the assigned projects keeping the deadlines and establishing a direct communication with the client
* Technical document management associated with the studies (standard procedures, certificates of analysis, deviations, OOS’s, CAPA’s, etc.)
* The direction and supervision of the experimental work of the technical staff in charge.
Here's what they offer:
* Competitive salary package commensurate with the qualifications and experience of the candidate.
* Full-time permanent contract
* Monday to Friday from 6am to 2pm
Compromiso con la Igualdad de Oportunidades:
En Solutia GHS garantizamos que todos nuestros procesos de selección se desarrollan en base a criterios objetivos, valorando únicamente las competencias, la experiencia y el talento de las personas candidatas.
Promovemos la igualdad de oportunidades y no toleramos ningún tipo de discriminación por razón de sexo, género, edad, origen, raza, religión, orientación sexual, identidad de género, discapacidad o cualquier otra circunstancia personal o social.
Asimismo, nuestra política retributiva se rige por el principio de equidad salarial ante el desempeño de las mismas funciones, reforzando nuestro compromiso con un entorno laboral diverso, inclusivo y respetuoso.
Requisitos:
* Degree in Biochemistry, Biotechnology, Chemistry or related
* Experience in HPLC methods.
* Experience in working in quality control in Pharmaceutical Company and GMP environments is a must.
* Knowlegde of electrophoretic techniques, Western-Blot and ELISAs and Quality Control of Proteins will be a plus.
* Good command of English.