Location: Warsaw & Madrid/Barcelona– hybrid work Type: Full-time What you’ll be doing CMC Activities Lead complex CMC projects and provide strategic advice on pharmaceutical development, manufacturing, testing, lifecycle management, and global regulatory requirements; Coordinate the preparation, review, and submission
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
If you’re interested in this role, please apply in English and include an English version of your Resume/CV. The Role: Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a
Job Overview Responsible for Drug Development Program Leadership services. Provides leadership and oversight for the successful delivery of complex pharmaceutical and biotechnology development programs across all stages of development. Leads integrated cross-functional teams and serves as a senior strategic
How Youll Make An Impact Provide technical consulting services that leverage Ecolab’s expertise in chromatography resin performance, downstream purification, and regulatory change management to help commercial teams understand customer needs and increase account revenue. Act as
Job Overview Responsible for Drug Development Program Leadership services. Provides leadership and oversight for the successful delivery of complex pharmaceutical and biotechnology development programs across all stages of development. Leads integrated cross-functional teams and serves as a senior strategic
We are looking for a Senior Software Engineer - AI Product development to join our Cortellis CMC team in Barcelona and help build the next generation of AI-powered solutions for the pharmaceutical industry. Es esencial asegurarse de que
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Oxford Global Resources is seeking a Global CMC Regulatory Affairs Manager Consultant to support as external contractor on behalf of Oxford a top leading pharma company to support headquarters in Barcelona through our consulting services division. Key
We’re looking for a Senior Software Engineer - AI Product development to join our Cortellis CMC team in Barcelona , where you’ll work on high-impact backend services that power global pharmaceutical innovation. In this role, you’ll take strong
Introduction to role: This role is based in Barcelona , with an on-site commitment of three days a week. Fluency in English is required. Asegúrese de que toda la información de su solicitud está actualizada y
Introduction To Role This role is based in ¿No sabe con seguridad qué habilidades necesitará para esta oportunidad? Simplemente lea la descripción completa a continuación para obtener una idea clara de los requisitos del candidato. This
About the profile About MIGx MIGx is a global consulting company with an exclusive focus on the healthcare and life science industries, with their particularly demanding requirements on quality and regulatory aspects. We have been managing
Regulatory Affairs Biosimilar Specialist LATAM Puede obtener más detalles sobre la naturaleza de esta vacante y lo que se espera de los solicitantes leyendo la información a continuación. In a nutshell Position: Regulatory Affairs Biosimilar Specialist
SpliceBio is a biotechnology company developing the next generation of genetic medicines through its proprietary Protein Splicing platform. Our mission is to unlock the potential of gene therapy by enabling the delivery of therapies beyond the
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Position: Regulatory Affairs Biosimilar Specialist LATAM Location: Madrid Experience: 5+ years in Regulatory Affairs within innovative biopharmaceuticals and/or biosimilars Want to know more? At Exeltis, we continue to grow and we are looking for a Regulatory
KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain (Cerdanyola del Vallés- Barcelona), Italy (Monsano-Ancona), Germany (Frankfurt), Denmark (Copenhagen) and a Liaison office in South Korea
LOCATION: SWITZERLAND OR SPAIN Habilidades, experiencia, cualificaciones. Si tiene el perfil adecuado para esta oportunidad, asegúrese de inscribirse hoy mismo. MAIN TASKS: Performance Management & KPIs Define and implement a comprehensive R&D performance framework, including KPIs,
# Director of Clinical Pharmacology and Quantitative PharmacologyBarcelona, , SpainApply NowFind out how well you match with this job Inscríbase rápido, consulte la descripción completa desplazándose hacia abajo para conocer todos los requisitos de este puesto.
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