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Clinical Quality Assurance & Training Lead – CROVELIS Localización: Madrid Experiencia: 5-7 años en Quality Assurance dentro de clinical research, pharma, biotech o healthcare, con experiencia en liderazgo de calidad o gestión de operaciones clínicas. La oportunidad En CROVELIS buscamos incorp

Whitewater Group is a leading provider of innovative and sustainable water treatment engineering systems operating in Ireland, the UK and across Europe in the Data Centre, Pharma, Power and Industrial sectors. We specialise in designing, installing, commissioning and maintaining water treatment solutions to meet our clients' specific needs. Our team is dedicated to delivering high‑quality, cost‑effective engineering solutions that prioritise safety, reliability and environmental sustainability. Compruebe a continuación si tiene lo necesario para esta oportunidad y, si es así, envíe su solicitud lo antes posible. Whitewater Group is headquartered in Naas, Co. Kildare and operates from European bases in Spain, Sweden, Finland and the UK, with plans for further offices in Germany, Denmark and Italy. The Group is experiencing significant growth driven by its focus on off‑site construction methods (OSM) for delivering turnkey projects, reducing on‑site construction time to a minimum. Job Outline The Commissioning Support Engineer will provide full documentation and administrative support to the Whitewater Group Commissioning Team across multiple water treatment and data‑centre projects. The role is focused on the preparation, control, organisation and continuous improvement of all commissioning‑related documents and workflows. Key responsibilities include: • Developing, formatting and maintaining commissioning documents including Sequences of Operation (SOOs), Level 2/3/4/5 test scripts, SAT documentation and other project‑specific commissioning deliverables., • Ensuring all documentation meets Whitewater Group standards, is consistent across projects and is delivered within required timelines., • Acting as the central point of control for project documentation: tracking required documents, version control, ensuring completeness and coordinating updates from the commissioning team., • Supporting Commissioning Engineers by preparing document packages for each project stage and ensuring the correct documentation is available for internal teams and external stakeholders., • Reviewing project information (P&IDs, IO lists, instrument lists, vendor documentation) to ensure alignment and accuracy across commissioning deliverables., • Collaborating closely with the Commissioning Lead and wider commissioning team to update and refine documents as system designs evolve., • Maintaining structured digital filing systems for all commissioning documentation and ensuring consistent document organisation across the company., • Contributing to continuous improvement of documentation templates, standards and internal processes to support team efficiency. Qualifications Our ideal candidate will be self‑motivated with a high level of energy, capable of working independently and within a team. This position demands a strong detail‑oriented work style, excellent oral and written communication skills and an accommodating proactive attitude. Additional qualifications required include: • Degree or equivalent qualification in Electrical or Automation Engineering., • Minimum five years’ experience in a similar role with design emphasis on the Data Centre, Industrial, Municipal and Pharma sectors an advantage., • Excellent technical writing and communication skills., • Fluent English speaker with strong speaking skills as the position will require presentations to clients., • Strong project management skills., • Experience working in a multi‑disciplinary team (process, electrical, automation engineering and commissioning)., • IT literate and proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook and MS Project)., • Proficiency in 2D/3D CAD and Revit is an advantage., • Proficiency in Procore an advantage., • Clear career development path within a growing and dynamic company. xqbhyrx, • Exposure to a variety of complex and high‑impact engineering projects across Ireland, the UK, Europe and America. Seniority level: Mid‑Senior level Employment type: Full‑time Job function: IT Services and IT Consulting and Engineering Services #J-18808-Ljbffr

¿Te apasiona Regulatory Affairs y quieres contribuir al desarrollo de nuevos tratamientos? En Crovelis, la CRO del grupo Insud Pharma, seguimos creciendo y buscamos incorporar un/a Senior Regulatory Affairs Specialist para unirse a nuestro equipo de Clinical Operations en Madrid. Si tienes experiencia gestionando ensayos clínicos internacionales, trabajando con CTIS, el European Clinical Trials Regulation (EU CTR 536/2014) y procesos regulatorios con la FDA, esta puede ser la oportunidad que estabas esperando. En pocas palabras Posición: Senior Regulatory Affairs Specialist Ubicación: Madrid, España Experiencia: +5 años en Regulatory Affairs dentro de ensayos clínicos ¿Cuál será tu misión? Serás una pieza clave en la estrategia regulatoria de estudios clínicos internacionales, coordinando todas las actividades regulatorias desde el start-up hasta el cierre del estudio y garantizando el cumplimiento de los requisitos regulatorios en Europa y Estados Unidos. Trabajarás de forma transversal con equipos de Clinical Operations, Medical Writing, Pharmacovigilance, Quality, sponsors y autoridades regulatorias, contribuyendo al éxito de proyectos con impacto real en el desarrollo de nuevos medicamentos. ¿Qué buscamos? Buscamos un perfil con experiencia demostrada en: Regulatory submissions mediante CTIS. Gestión del ciclo de vida regulatorio de ensayos clínicos. Preparación de submissions a la FDA (INDs y otras interacciones regulatorias). Resolución de Requests for Information (RFIs). Coordinación con autoridades regulatorias y comités éticos. Conocimiento sólido de ICH-GCP, normativa europea y regulación internacional. Valoraremos especialmente experiencia en entornos internacionales, CROs y proyectos multicéntricos. ¿Qué encontrarás en Crovelis? Formar parte de una CRO en pleno crecimiento dentro de un grupo farmacéutico internacional. Participar en proyectos clínicos estratégicos con alcance global. Colaborar con equipos multidisciplinares altamente especializados. Un entorno donde podrás seguir desarrollando tu carrera profesional y asumir nuevos retos. ¿Te interesa? Si buscas un proyecto con impacto internacional y quieres formar parte de un equipo que contribuye al desarrollo de nuevas terapias para los pacientes, nos encantará conocerte. Puedes enviar tu candidatura a través de LinkedIn o compartir esta publicación con alguien a quien pueda interesarle. #Crovelis #InsudPharma #ClinicalResearch #RegulatoryAffairs #ClinicalTrials #LifeSciences #HealthcareJobs #ClinicalOperations #Hiring #InsudTalent En Crovelis promovemos la igualdad de oportunidades y creemos en equipos diversos e inclusivos. Todas las candidaturas serán valoradas exclusivamente en función de su experiencia, competencias y potencial, sin distinción de género, edad, origen, orientación sexual, discapacidad o cualquier otra condición protegida por la legislación vigente.

Whitewater Group is a leading provider of innovative and sustainable water treatment engineering systems operating in Ireland, UK and across Europe in the Data Centre, Pharma, Power and Industrial sectors. We specialise in designing, installing, commissioning, and maintaining water treatment solutions to meet our clients' specific needs. Our team is dedicated to delivering high-quality, cost-effective engineering solutions that prioritize safety, reliability, and environmental sustainability. ¿Posee las habilidades y la experiencia adecuadas para este puesto? Siga leyendo para descubrirlo y envíe su solicitud. Whitewater Group is headquartered in Naas, County Kildare and operates from European bases in Spain, Sweden, Finland and the UK, with plans for further offices to open in Germany, Italy and Denmark. The Group is experiencing significant growth due to its focus on off-site construction methods (OSM) of delivering turnkey projects, meaning on-site construction time is kept to a minimum. The Opportunity Due to continued expansion, we are seeking a Procurement Specialist who will be responsible for managing technical purchasing activities while supporting logistics coordination and supplier expediting to ensure timely and cost-effective delivery of materials and equipment for industrial water treatment projects. This role plays a key part in ensuring project schedules are met, supplier performance is monitored, and procurement processes run efficiently in collaboration with Engineering and Project Management teams. Main Duties and Responsibilities Procurement • Manage end-to-end purchasing processes for project-related materials and equipment., • Prepare and issue RFQs, evaluate supplier quotations and negotiate commercial terms., • Issue purchase orders and ensure contractual compliance., • Identify, qualify and develop reliable suppliers., • Maintain procurement documentation and cost control tracking. This position will collaborate and provide support in logistics and expediting tasks • Liaise with freight forwarders and logistics partners., • Ensure compliance with Incoterms, customs regulations and transport requirements., • Support inventory coordination and material receipt processes., • Monitor supplier production schedules and delivery milestones., • Proactively follow up on purchase orders to prevent delays., • Provide regular status reports to Project Managers and internal stakeholders. Requirements • Bachelor’s degree in Engineering, Business, Supply Chain or related field., • Minimum 5 years of proven experience in procurement, logistics support and expediting within industrial or EPC project environments., • Experience in water treatment, process industry, energy or industrial plant projects is highly valued., • Strong knowledge of purchasing processes, supplier negotiations and international logistics., • Experience working with ERP systems and advanced Excel skills. xqbhyrx, • Fluent English (written and spoken). Spanish is a plus, • Competitive Salary for the right candidate, • Opportunity for career progression within a rapidly growing company, • Hybrid working model Health& Life Insurance and Pension Plan #J-18808-Ljbffr

Consultant Regulatory Affairs No deje pasar esta oportunidad, inscríbase rápidamente si su experiencia y habilidades coinciden con lo que se indica en la siguiente descripción. Location: Hybrid - Madrid Type: Full-time The QbD Group supports life sciences companies worldwide from idea to patient. QbD's team offers knowledge&tailored (software) solutionsin development, clinical, regulatory & compliance, production and distribution for companies active inATMP, Biotech, Medical Devices, In Vitro Diagnostics, Digital Health and Pharma. QbD has affiliates in 8 different countries and can count on the expertise of more than 500 life science professionals and growing. What’s in it for you? Make a real impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devices Grow within a community of experts:Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise. Build a meaningful career:As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences. A fair, competitive package: We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be valued. What you’ll be doing • Review and approve promotional and non-promotional materials for medicinal products, medical devices in accordance with applicable national and EU regulations, industry codes, and company procedures., • Provide regulatory advice regarding advertising, promotional claims, scientific communications, educational materials, and patient-facing content., • Assess compliance of marketing and communication materials before external use., • Collaborate closely with Medical Affairs, Marketing, Legal, Quality, and Regulatory Affairs teams., • Support the preparation, maintenance, and lifecycle management of marketing authorizations., • Contribute to regulatory submissions, variations, renewals, and compliance activities., • Monitor regulatory developments related to pharmaceutical advertising and promotional practices., • Support audits, inspections, and internal compliance initiatives where required., • Maintain documentation and records in accordance with internal quality systems. What you bring Qualifications & Experience • University degree in Pharmacy, Life Sciences, Medicine, or a related scientific discipline., • At least 3-5 years of experience in Regulatory Affairs within the pharmaceutical industry., • Proven experience in review and approval of promotional and non-promotional materials., • Strong knowledge of Spanish pharmaceutical advertising requirements and relevant EU legislation., • Experience working in a cross-functional and international environment., • Excellent written and verbal communication skills in Spanish and English., • Strong attention to detail and ability to manage multiple priorities. Preferred Qualifications • Knowledge of medical information, scientific communications, and compliance processes., • Experience supporting multiple pharmaceutical products and therapeutic areas. Who you are Our culture is driven by values If this sounds like you, you'll fit right in: • You’re resilient and tackle challenges with a positive mindset, • You’re curious and always up for learning something new, • You have a no non-sense approach honest, clear, respectful, • You’re innovative and bring ideas, not just opinions, • And above all, you’re serious about your work, but not too serious about yourself About us We support life sciences companies from idea to patient — offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 500+ experts across 8 countries, we help drive innovation in ATMP, biotech, medical devices, diagnostics, digital health, and pharma. We believe in JPEG: Joy. Partnership. Going the Extra Mile. Getting Things Done. xqbhyrx You won't just be taking a job — you'll be joining a community where people grow, laugh, build, and contribute to something bigger. #J-18808-Ljbffr

QbD Group seeks an Associate Consultant Drug Safety to join its hybrid Madrid team. ¿Le interesa este puesto? Puede encontrar toda la información relevante en la descripción a continuación. You will support pharmacovigilance activities for pharma, biotech and medical device clients, handling PV cases and regulatory submissions with a focus on quality and compliance. The role requires a strong background in life sciences, fluency in English and German, and a proactive, detail-oriented mindset. xqbhyrx The position offers a collaborative environment and growth opportunities within a global life sciences #J-18808-Ljbffr Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

Associate Consultant Drug Safety Sea uno de los primeros solicitantes, lea la descripción completa del puesto a continuación y luego envíe su candidatura para que sea considerada. Location: Hybrid - Madrid Type: Full-time The QbD Group supports life sciences companies worldwide from idea to patient. QbD’s team offersknowledge&tailored (software) solutionsin development, clinical, regulatory & compliance, production and distribution for companies active inATMP, Biotech, Medical Devices, In Vitro Diagnostics, Digital Health and Pharma. QbD has affiliates in 8 different countries and can count on the expertise of more than 500 life science professionals and growing. What’s in it for you? Make a real impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devices Grow within a community of experts:Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise. Build a meaningful career:As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences. A fair, competitive package: We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be valued. What you’ll be doing General Responsibilities: • The performance of tasks and duties of instrumental and highly predictable content in accordance with previously established instructions according to the rules, guidelines or ordinary procedures in regular use in the company, tasks for which they have the direct supervision of the immediate superior., • Every staff member of the Pharmacovigilance Department should be trained in each applicable SOP and WI according to general procedure, • Depending on the projects, specific training in applicable client’s SOPs is also mandatory. Specific responsibilities: • Cases management control, • Data entry and quality control of PV cases in post-marketing and clinical trials, or related to medicinal products, medical devices and cosmetics., • PV Assessment of any case of suspected adverse reaction., • Direct contact with HCP and patients/consumers., • Perform any follow up activities required., • Submission of cases to Eudravigilance, MHRA or any other Competent Authority., • Perform bibliographic searches in local scientific journals, international journals, MLM service and any other type of search., • Management of medical information and answer of queries., • Review and control of Safety Regulatory intelligence, • Review and control of Pharmacovigilance quality system, • Participation in specific events related to their area of work. What you bring Education: • Bachelor's degree in Life Sciences or related, • Master's degree in Pharmacovigilance, Pharmaceutical Industry or related. Desirable. Experience: Work experience as Trainee or Junior within pharmacovigilance and updated knowledge in Quality Assurance for the Pharmaceutical Industry is a plus. • Bibliographic search and database management. Desirable, • Knowledge of European Good Pharmacovigilance Practices (GVPs)., • Knowledge regarding Eudravigilance requirements for Marketing Authorization, • Holders (clients) and the processes with the Health Competent Authorities. Desirable Languages: • High level of English. Must., • Proficient level of German. Must. Other: • Good teamwork skills and high learning capacity is considered a plus., • Participative and proactive in work groups., • Attention to detail, • Skills and/or experience in the writing of scientific texts. Desirable, • Organization ability and task prioritization. Who you are Our culture is driven by values If this sounds like you, you’ll fit right in: • You’re resilient and tackle challenges with a positive mindset, • You’re curious and always up for learning something new, • You have a no non-sense approach honest, clear, respectful, • You’re innovative and bring ideas, not just opinions, • And above all, you’re serious about your work, but not too serious about yourself About us We support life sciences companies from idea to patient — offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 500+ experts across 8 countries, we help drive innovation in ATMP, biotech, medical devices, diagnostics, digital health, and pharma. We believe in JPEG: Joy. Partnership. Going the Extra Mile. Getting Things Done. xqbhyrx You won’t just be taking a job — you’ll be joining a community where people grow, laugh, build, and contribute to something bigger. #J-18808-Ljbffr

Optimaes Talent is recruiting a Global Commercial Director for a biopharmaceutical client focused on allergen immunotherapy and diagnostics.

Roche Holding AG à Madrid recherche un Senior IT Validation Professional pour piloter l’évaluation, la conception, le développement et l’approbation des livrables de qualification et des plans de validation pour des systèmes informatisés GMP/GxP.Vous travaillerez en équipe pour garantir la

Ready to build scalable cloud data platforms that power analytics and business intelligence??.No deje pasar esta oportunidad, inscríbase rápidamente si su experiencia y habilidades coinciden con lo que se indica en la siguiente descripción.Join our expert team to work on a.You will apply your kno

Insud Pharma is seeking a Commercial & Financial Controller to join our Madrid team and oversee global, transversal Finance/Controlling activities across international entities.

Can you imagine building AI‑powered products that transform how business teams generate strategic insights? Join our expert team to work on a Pharmaceutical sector product, contributing to the development of an AI platform that transforms enterprise knowledge into intelligent decision support.

En Insud Pharma, buscamos incorporar un/a Study Coordinator para un ensayo clínico fase III en el área de salud de la mujer. The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and tre

Todo ello para nuestra marca Pfeiffer orientada hacia soluciones de alto vacío (sectores de pharma, equipamiento médico, laboratorios, etc.

ROVI Pharma Industrial Services busca un Técnico/a QA Compliance para su planta de Julián Camarillo, Madrid, para asegurar el cumplimiento de GMP y del sistema de Calidad de la compañía.

Alexion España busca un Regional Account Manager para Madrid, Castilla y León y Canarias, orientado a enfermedades raras y oncología.Para una comprensión completa de esta oportunidad y de lo que se requerirá para ser un candidato exitoso, siga leyendo.Desarrollarás relaciones con líderes de o

Experience in Pharma, Chemicals or Biochemical industries is also valued.

At Astek Iberia, we are looking for.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.A degree in Information Technology, Business Administration, Engineering, or a related fiel

Unolab Manufacturing, CDMO español con más de 20 años de experiencia en fabricación de productos sanitarios y medicamentos, busca un/a Business Development Manager para impulsar crecimiento y gestionar relaciones con clientes internacionales.Todo listo para enviar su solicitud? Por favor, lea la

Johnson & Johnson, a leader in healthcare, seeks a Post Doctoral Researcher in Data Analytics & Computational Sciences to design evaluation frameworks for GenAI tools used in pharmaceutical R&D.

Roche Holding AG, situé à Madrid, recherche un Senior Data Product Owner passionné pour piloter des solutions de données innovantes.Presente su candidatura después de leer los siguientes requisitos de habilidades y cualificaciones para este puesto.Vous serez responsable de la gestion des produi

IQVIA Pharma Review specializes in delivering high‑quality scientific content solutions that support pharma and biotech teams across the product lifecycle. With deep expertise in scientific review and approval, Pharma Review enables organizations to accelerate the review and approval of clear, acc

Insud Pharma is seeking a Junior Legal Counsel – Litigation to join its Legal Department in Madrid.

Etihad Airways is seeking a Cargo Sales Officer to drive sales growth in the pharma-focused cargo division. You will lead performance reviews, coach teams, and ensure safety and quality procedures are followed to deliver high-performance outcomes for pharmaceutical shipments.

INSUD PHARMA is accelerating the digital transformation of HR by leveraging automation, AI agents, and digital applications to improve operational efficiency and employee experience.

A leading healthcare agency in Madrid seeks an Account Director AOR to oversee multiple brands and lead strategic recommendations.Por favor, asegúrese de leer completamente el resumen y los requisitos de esta oportunidad de empleo que se detallan a continuación.This role requires an authoritative

Turner & Townsend in Madrid is seeking a Cost Manager to oversee cost planning, estimating, and reporting for complex real estate, infrastructure, and industrial projects, acting as day-to-day interface with clients.Por favor, verifique que tiene el nivel de experiencia y las cualificaciones adecuad

A leading digital solutions company in Spain is seeking a Market Research Project Manager to support global pharmaceutical research initiatives.

Se requiere más de 6 años de experiencia en el sector pharma, en donde se valora la gestión de stakeholders y el trabajo en entornos ágiles.

En nuestra planta de producción de Julián Camarillo, buscamos un Ingeniero/a de mantenimiento de instalaciones para desempeñar las siguientes funciones:.Planificación de tareas de mantenimiento.Gestionar mantenimiento preventivo/correctivo/ predictivo.Soporte en Mantenimiento legal de planta.Tit

Can you imagine building the backend of an innovative Agentic AI solution?.Todo listo para enviar su solicitud? Por favor, lea la descripción al menos una vez antes de hacer clic en "Solicitar".Join our expert team to work on an AI-focused project, contributing to the development and evolution of a

Compartir toda la información relevante con el equipo de Alexion Pharma en el país.

Una empresa farmacéutica líder ubicada en Madrid busca un/a Project Manager para el Departamento de Nuevos Productos.A continuación se detalla todo lo que necesita saber sobre lo que implica esta oportunidad, así como lo que se espera de los solicitantes.El candidato ideal tendrá una licenciatu

At Roche you can show up as yourself, embraced for the unique qualities you bring.Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.This is how we

Si está considerando enviar una solicitud, asegúrese de pulsar el botón de solicitar de abajo después de leer la descripción completa.Te gustaría liderar proyectos estratégicos de.Departamento de Nuevos Productos.Gestión y planificación del proyecto:.Elaborar el Plan de Transferencia de Tec

The activities of INSUD PHARMA are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more tha

Ashfield Healthcare en Madrid busca un/a Client Solutions Manager para liderar programas PSP, impulsar ventas y desarrollar negocio en el ecosistema farmacéutico y sanitario.Por favor, asegúrese de leer atentamente los siguientes detalles antes de enviar cualquier solicitud.Se trabajará con un en

This strategic role encompasses developing sales plans, managing sales teams, and maintaining key customer relationships in the pharmaceutical logistics sector.

RED Global is seeking an experienced SAP EWM Project Manager to lead a major SAP EWM deployment in a pharmaceutical environment.

Senior Solution Architect – design business‑driven, standards‑based, future‑ready solutions to enable Roche’s omnichannel orchestration capabilities.Build and scale an integrated ecosystem leveraging Adobe Experience Platform (RT‑CDP, AJO, CJA), ensuring alignment with enterprise archite

Are you ready to drive Data Governance initiatives and collaborate with cross functional stakeholders in an international environment?.Está considerando presentar su candidatura para este trabajo? Compruebe todos los detalles en esta descripción del puesto y luego haga clic en "Solicitar".Join our

Tech Mahindra is seeking a Solution Architect for Pharma Technical Operations to guide strategic architecture across pharma/diagnostics with a focus on business processes, data architecture, and technology strategy. The role xcskxlj requires deep Pharma domain expertise, TOGAF certification, and str

ATIKA PHARMA busca delegados/as de ventas para promover sus productos en médicos, hospitales, farmacias y otros profesionales de la salud en la zona asignada.

Our Mace consultancy pharmaceutical and life sciences sector set out to make a difference in the industry. We’re currently looking for an experienced project controls engineer (German speaking) to join our growing pharma team.

Estamos buscando un/a Pharma Specialist Technician apasionado/a y comprometido/a!.

At Roche you can show up as yourself, embraced for the unique qualities you bring.Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.This is how we

LETI Pharma somos una compañía biofarmacéutica, independiente y de capital familiar. En LETI Pharma creemos en las personas, por eso promovemos un entorno laboral diverso e integrador, promoviendo la transparencia y la confianza mutua a través de la comunicación abierta. Asegurar una atención