Location: Barcelona - Spain or Cambridge - UK (3 days in-office requirement) About AstraZeneca and AISI At AstraZeneca, technology and science meet to change what is possible for patients. We are building a connected, end-to-end Enterprise
Posted date Jun. 27, 2026 Contract type Full time Job ID R- Descubra si esta oportunidad es adecuada para usted leyendo toda la información que sigue a continuación. Why choose AstraZeneca Spain? AstraZeneca Spain is a
Principal Executive Search Consultant - Medical & Clinical Clinical Project Manager – Phase I PK/PD & Bioequivalence Studies (Generics) Location: Spain Employment Type: Full-time, Permanent About Us Im working with a forward thinking pharmaceuticals who are
Principal Executive Search Consultant - Medical & Clinical Clinical Project Manager – Phase I PK/PD & Bioequivalence Studies (Generics) Location: Spain Employment Type: Full-time, Permanent About Us Im working with a forward thinking pharmaceuticals who are
Principal Executive Search Consultant - Medical & Clinical Clinical Project Manager – Phase I PK/PD & Bioequivalence Studies (Generics) Location: Spain Employment Type: Full-time, Permanent About Us Im working with a forward thinking pharmaceuticals who are
Principal Executive Search Consultant - Medical & Clinical Clinical Project Manager – Phase I PK/PD & Bioequivalence Studies (Generics) Location: Spain Employment Type: Full-time, Permanent About Us Im working with a forward thinking pharmaceuticals who are
Role Location: Madrid, Spain or Milan, Italy - Hybrid Remuneration: Competitive salary and benefits Cpl Life Sciences is partnering with a leading international pharmaceutical organisation to recruit a CMO QA Manager. This is an exciting opportunity
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
Desde Quales, buscamos a un/una IT Compliance Junior, con al menos 1 año de experiencia, para una importante industria farmacéutica, en una de sus plantas en Azuqueca de Henares. Responsabilidad Global: Establecer el aseguramiento de la
Desde Quales, buscamos a un/una IT Compliance Junior, con al menos 1 año de experiencia, para una importante industria farmacéutica, en una de sus plantas en Azuqueca de Henares. Responsabilidad Global: Establecer el aseguramiento de la
Desde Quales, buscamos a un/una IT Compliance Junior, con al menos 1 año de experiencia, para una importante industria farmacéutica, en una de sus plantas en Azuqueca de Henares. Responsabilidad Global: Establecer el aseguramiento de la
Desde Quales, buscamos a un/una Si los siguientes requisitos del puesto y la experiencia coinciden con sus habilidades, por favor, asegúrese de enviar su solicitud sin demora. IT Compliance Junior, con al menos 1 año de
Overview La siguiente información tiene como objetivo proporcionar a los posibles candidatos una mejor comprensión de los requisitos para este puesto. The QbD Group supports life sciences companies worldwide from idea to patient. QbD’s team offers
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
Descripción del trabajo Experteer Overview In this role you drive global regulatory compliance and quality operations within GxP environments, partnering with cross-functional teams to enable compliant, scalable business practices. You’ll lead controlled document governance, training governance,