descripción del trabajo

pstrongMAIN DUTIES RESPONSIBILITIES /strong /pulliPrepare analytical batches to quantify drugs, anti-drugs antibodies or biomarkers in biological matrices by ligand binding assays (ELISA, MSD) according to international guidelines and internal procedures. /liliPerform the evaluation and treatment of results of analytical batches. /liliLabel proteins with biotin or Sulfo-tag. /liliSupport the Study Director in: (i) the resolution of problems, (ii) the preparation of SOPs and other study documentation. /liliCarry out maintenance and calibration/verification of laboratory equipment. /liliActively support Laboratory Management in evaluating and implementing new processes and equipment. /li /ulpbr/ppstrongREQUIRED PROFILE QUALIFICATIONS /strong /pulliPhD, MSc or BSc in biology or related subject. /liliMinimum 1-year experience in bioanalytical laboratories. /liliExperience working with ELISA, MSD or other Ligand Binding techniques.   /liliUnderstanding of international bioanalytical guidelines, and experience working under GLP/GCP regulations. /liliExperience working with LIMS systems and with cell culture and qPCR techniques will be valued. /liliExcellent level of English (Spanish – nice to have). /liliProficiency in MS-Office, especially Word and Excel. /li /ulpbr/ppstrongOTHER REQUIRED SKILLS /strong /pulliStrong communications and organization skills, and capacity to work in teams. /liliProactive and hands-on approach. /liliHigh level of motivation and enthusiastic personality. /li /ulpbr/ppstrongWHAT IS OFFERED /strong /pulliOpportunity to work and contribute to the success of an expanding CRO. /liliSolid scientific team with career growth opportunities. /liliCutting edge laboratory with the latest technology. /liliInternational and multicultural environment in company based in Barcelona. /liliDiligent, professional organization, with a human touch. /li /ulpbr/ppstrongCOMPANY DESCRIPTION /strong /ppAnapharm Bioanalytics is a customer-driven Contract Research Organization (CRO) specializing in small and large molecule bioanalysis. With over 30 years of expertise in method development, validation, and sample analysis, the company supports drug development for pharmaceutical and biotechnology industries globally. Anapharm leverages advanced LC-MS/MS and LBA technologies to deliver services such as PK studies, biomarker testing, and immunogenicity assays for preclinical and clinical phases. The organization maintains strict compliance with GLP and GCP standards, having successfully passed multiple regulatory inspections by authorities such as the FDA and EU Health Authorities. Through a global network of partners, Anapharm offers robust full-service solutions for drug development and regulatory approval. /p