Personas extraordinarias, confiadas por los clientes para diseñar y avanzar en el mundo. Wood está buscando profesional en administración, Ingeniería o afines, con experiencia superior a un año específica en proyectos de ingeniería dentro del sector
Join Rephine Barcelona: Leading Life Sciences Quality Worldwide At Rephine, we set the standard for quality assurance and GxP compliance in the Life Sciences industry. With offices in Barcelona, the UK, and China, India, we support
Join Rephine Barcelona: Leading Life Sciences Quality Worldwide At Rephine, we set the standard for quality assurance and GxP compliance in the Life Sciences industry. With offices in Barcelona, the UK, and China, India, we support
Join Rephine Barcelona: Leading Life Sciences Quality Worldwide At Rephine, we set the standard for quality assurance and GxP compliance in the Life Sciences industry. With offices in Barcelona, the UK, and China, India, we support
Join Rephine Barcelona: Leading Life Sciences Quality Worldwide At Rephine, we set the standard for quality assurance and GxP compliance in the Life Sciences industry. With offices in Barcelona, the UK, and China, India, we support
Join Rephine Barcelona: Leading Life Sciences Quality Worldwide At Rephine, we set the standard for quality assurance and GxP compliance in the Life Sciences industry. With offices in Barcelona, the UK, and China, India, we support
Join Rephine Barcelona: Leading Life Sciences Quality Worldwide At Rephine, we set the standard for quality assurance and GxP compliance in the Life Sciences industry. With offices in Barcelona, the UK, and China, India, we support
Bristol Myers Squibb is seeking a Senior Documentation Specialist to independently manage eDMS processes, publish regulatory documents, and collaborate with GSRD and external authors. The role involves mentoring, ensuring submission-ready formatting, and coordinating protocol and CSR documents
Bristol Myers Squibb is seeking a regulatory documentation lead to drive end-to-end workstreams for submissions and eDMS processes. You will coordinate internal teams and external authors, ensuring submission readiness across HA activities and complex protocol documents. This
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to
Wir sind Qualitice, eine GxP-Beratung mit Sitz in Barcelona. Unsere Kunden sind Pharma-, Biotech- und Medizintechnikunternehmen im deutschsprachigen Raum. Wir liefern das, was in regulierten Systemeinführungen wirklich zählt: belastbare Validierung, Projekte, die den Termin halten, und