How You’ll Make an Impact: The Director, Clinical Development – EMEAI serves as the senior regional Clinical Development leader and primary clinical liaison for the EMEAI region. This role supports global clinical development programs across primarily
We’re building the future of medical dermatology by focusing on unmet patient needs and giving people the space to think independently, take ownership and make an impact that matters. Our purpose is simple: to transform patients’
A leading consulting firm is seeking a Global CMC Regulatory Affairs Manager Consultant to support a top pharmaceutical company in Barcelona. ¿Listo para inscribirse? Antes de hacerlo, asegúrese de leer todos los detalles pertenecientes a este trabajo
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization
Job Title: Senior Director, Regulatory Affairs Strategy - Cell and Gene Therapy Available locations: Barcelona, Spain Amsterdam, Netherlands Introduction to role: Are you ready to set the global regulatory vision for pioneering cell and gene therapies and
Regulatory Consultant - CMC (CMC with small molecule products) Envíe su CV y cualquier información adicional requerida después de haber leído esta descripción, haciendo clic en el botón de solicitud. Syneos Health® is a leading fully-integrated life sciences
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization
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
Experteer Overview Para ser considerado para una entrevista, por favor, asegúrese de que su solicitud se ajusta plenamente a las especificaciones del puesto que se encuentran a continuación. In this role you will provide expert technical
Authoring of CMC sections (Drug Product and/or Drug Substance) for new registration applications in CTD format, in alignment with global regulatory strategies and current regulatory guidelines. Authoring and reviewing CMC documentation to support variations and commitments resulting from interactions
Almirall SA in Sant Feliu de Llobregat seeks an experienced Associate Director, Regulatory Affairs to lead global regulatory strategies and submissions for our dermatology portfolio. Obtenga más información sobre las tareas generales relacionadas con esta oportunidad a
Italfarmaco is seeking an experienced candidate in Alcobendas, Spain to author and review CMC sections for drug registration applications. ¿Todo listo para enviar su solicitud? Asegúrese de comprender todas las responsabilidades y tareas asociadas a este puesto
Almirall SA in Sant Feliu de Llobregat seeks an experienced Associate Director, Regulatory Affairs to lead global regulatory strategies and submissions for our dermatology portfolio. You will collaborate with Clinical, CMC, Safety and Market Access teams, coordinate CTAs,
The Company Si desea saber un poco más sobre esta oportunidad, o está considerando presentar su candidatura, por favor, lea la siguiente información del puesto. STALICLA is an international, clinical-stage neuropsychiatry company developing precision treatments for
The Corporate Business & Portfolio Development (B&PD) function is a core enabler of Italfarmaco’s strategic expansion. The role contributes directly to the identification, evaluation, and execution of external innovation opportunities, including licensing, partnerships, and acquisitions, in
# 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.
# ASSOCIATE DIRECTOR, REGULATORY AFFAIRSApplyremote type: R&D & Medical Affairslocations: SANT FELIU DE LLOBREGATtime type: Full timeposted on: Posted 2 Days Agojob requisition id: We’re building the future of medical dermatology by focusing on unmet patient
Position: Regulatory Affairs Biosimilar Specialist LATAM ¿Interesado en saber más sobre este trabajo? Desplácese hacia abajo y descubra qué habilidades, experiencia y cualificaciones académicas se necesitan. Location: Madrid Experience: 5+ years in Regulatory Affairs within innovative
# ASSOCIATE DIRECTOR, REGULATORY AFFAIRSPresenta candidaturaremote type: R&D & Medical Affairslocations: SANT FELIU DE LLOBREGATtime type: Full timeposted on: Offerta pubblicata 2 giorni fajob requisition id: Stiamo costruendo il futuro della dermatologia medica concentrandoci sui bisogni