HIPRA es una empresa farmacéutica y biotecnológica enfocada en la prevención y diagnóstico para salud animal y humana, con una amplia gama de vacunas altamente innovadoras y un avanzado servicio de diagnóstico. Tiene una sólida presencia internacional en más de 40 países con filiales propias, 11 centros de diagnóstico y 6 plantas de producción ubicadas estratégicamente en Europa (España) y América (Brasil). La investigación y el desarrollo constituyen el núcleo de su conocimiento. HIPRA dedica el 15% de su facturación anual a actividades de I+D que se concentran en la creación y aplicación de los últimos avances científicos para el desarrollo de vacunas innovadoras de la más alta calidad. Para darle un valor añadido a su experiencia en vacunación, la empresa también desarrolla dispositivos médicos y servicios de trazabilidad. The R&D Department at our HIPRA Campus in Aiguaviva (Girona) is actively seeking a highly skilled and driven R&D Researcher to join the Analytical Method Team for Human Health. We Are Looking For Candidates With PhD or postdoc in Biological or Chemical Sciences A minimum of 3 years of experience in biopharmaceutical analytical development, working with biologics (monoclonal antibodies, recombinant proteins, vaccines) Proven expertise in biochemical and immunological analytical methods such as ELISA, BLI/SPR, binding/affinity assays, potency assays, or antibody structural characterization and also with complementary physico-chemical techniques (HPLC/UPLC, CE-SDS, cIEF, MS, etc.). Demonstrated ability to design and execute analytical studies independently and translate findings into actionable conclusions. Proven ability to independently execute experimental protocols and meet project deadlines. Good communications skills, strong ability to work collaboratively within a multidisciplinary group and with external partners and ability to perform verbal and written scientific data presentations. Proficiency level of spoken and written English for daily task development At Hipra You Will Find Continuous learning. A rapidly expanding multinational company. A multicultural environment open to new ideas. Long term job positions. Main Responsibilities Lead the development and validation of biochemical and immunological analytical methods for the characterization of Drug Substance and Drug Product, including ELISA, BLI/SPR, potency assays, binding/affinity assessments and antibody structural or functional analysis. Contribute to method lifecycle management, comparability and stability studies. Drive collaboration with internal development teams (Process Development, Formulation, QC, QA) to align analytical strategies with project needs and coordinate analytical activities with CROs. Generate and review high-quality technical documentation—including method development reports, validation protocols/reports, and regulatory-compliant documents. Ensure scientific rigor and operational excellence, with strong experimental design, systematic troubleshooting, clear result interpretation, and full adherence to data integrity and good documentation practices. Provide technical guidance and mentorship within the team and actively contribute to problem solving and innovation in analytical development.
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