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If you are looking to collaborate with a growing international company and contribute your technical expertise to impactful internal projects, this is the right opportunity for you. OXON Epidemiology is a rapidly expanding international CRO seeking a mid-level SharePoint & Power Platform Developer to support and enhance its internal IT ecosystem. This role is designed for an external consultant, working on a flexible, hourly basis, collaborating closely with OXON’s IT and business teams. JOB DESCRIPTION The selected consultant will be responsible for designing, developing and maintaining internal SharePoint-based applications and workflows , supporting business processes across the organization. The role requires hands-on development using Microsoft SharePoint and Power Platform , with integration to databases and reporting tools. SharePoint & Power Platform Development: 2–3 years of experience working with Microsoft SharePoint (Online) Experience creating and customizing SharePoint sites, lists, libraries and permissions Strong hands-on experience with Power Apps for developing internal business applications Experience building and maintaining Power Automate workflows Experience integrating SharePoint and Power Apps with: SQL Server / Azure SQL Dataverse Experience consuming and exposing data through REST APIs Experience developing dashboards and reports using Power BI Solid knowledge of SharePoint Framework (SPFx) is a plus Programming & Technical Skills: Proficiency in JavaScript / TypeScript Good knowledge of HTML5, CSS3 Experience working with relational databases Familiarity with Azure services related to Microsoft 365 solutions Experience using version control systems (Git) Understanding of application lifecycle, testing and maintenance Additional Criteria: Strong communication skills, able to gather requirements and interact with non-technical stakeholders Good English level is an asset Ability to work independently with limited supervision Strong analytical and problem-solving skills Proactive attitude and willingness to learn Ability to manage multiple tasks and meet agreed deadlines WE OFFER: Flexible collaboration on an hourly consultancy basis Competitive hourly rate, aligned with experience Flexible working arrangements (remote/hybrid) Opportunity to collaborate with an international, growing organization Participation in real-world data and epidemiology projects with high impact OXON EPIDEMIOLOGY is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive, friendly and learning environment for all employees. We encourage applications from candidates of all backgrounds and do not discriminate based on race, gender, age, religion, disability, sexual orientation, or any other protected status. Join us in building a diverse, talented and happy team! COMPANY DESCRIPTION: OXON is a full service global scientific/operational service provider specialising in multi-country field, database and hybrid observational studies, and pragmatic trials, for safety, market access/HEOR and drug development. We are a preferred provider for several top 20 pharma companies. With offices in London, Madrid, and Kentucky, and strong links to the prestigious London School of Hygiene & Tropical Medicine, OXON applies world-class epidemiological and operational experience and innovative technologies to help clients worldwide obtain high-quality real-world data for improving patients' and public health. For more information, see:

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. Whitewater Group is headquartered in Bray, Co. Wicklow with a satellite office in Naas, Co. 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. Due to continued expansion, we now seek a Automation Engineer to work on various projects in Data Centre Sectors. Design and implementation of industrial automation systems (PLC, HMI, SCADA), with a special focus on Siemens technology (TIA Portal, Step7, WinCC). Development of control architectures, instrumentation integration and PLC programming. IO lists, control philosophy, logic diagrams, electrical drawings, data sheets, etc. Coordination and supervision of FAT and SAT tests, as well as support in the commissioning of installations. Technical leadership in multidisciplinary projects, from the design phase to the final delivery. Degree in Electrical, Electronic, Industrial Engineering or similar. Higher Level Training Cycle in Automation ~ More than 5 years of experience in industrial automation, preferably in the water sector, other industries being valid: Chemicals, food, pharma, logistics, automotive. ~ Advanced knowledge in the design of low-voltage electrical panels and international regulations (IEC, UL, NFPA). ~ Proficiency in industrial communication protocols (PROFINET, MODBUS TCP/RTU, Profibus, BACnet). ~ English level B2/C1 (essential for documentation and communication with international clients). ~Experience with redundant PLCs, Siemens S7-1500, ET200SP and HMI systems. Ability to lead technical teams and coordinate with other engineering disciplines. Social Benefits Hybrid Work and Flexible Hours

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. Whitewater Group is headquartered in Bray, Co. Wicklow with a satellite office in Naas, Co. 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. Due to continued expansion, we now seek a Automation Engineer to work on various projects in Data Centre Sectors. Design and implementation of industrial automation systems (PLC, HMI, SCADA), with a special focus on Siemens technology (TIA Portal, Step7, WinCC). Development of control architectures, instrumentation integration and PLC programming. IO lists, control philosophy, logic diagrams, electrical drawings, data sheets, etc. Coordination and supervision of FAT and SAT tests, as well as support in the commissioning of installations. Technical leadership in multidisciplinary projects, from the design phase to the final delivery. Degree in Electrical, Electronic, Industrial Engineering or similar. Higher Level Training Cycle in Automation ~ More than 5 years of experience in industrial automation, preferably in the water sector, other industries being valid: Chemicals, food, pharma, logistics, automotive. ~ Advanced knowledge in the design of low-voltage electrical panels and international regulations (IEC, UL, NFPA). ~ Proficiency in industrial communication protocols (PROFINET, MODBUS TCP/RTU, Profibus, BACnet). ~ English level B2/C1 (essential for documentation and communication with international clients). ~Experience with redundant PLCs, Siemens S7-1500, ET200SP and HMI systems. Ability to lead technical teams and coordinate with other engineering disciplines. Social Benefits Hybrid Work and Flexible Hours

Clinical Research Associate (CRA) Flexible (remote role) We are seeking an experienced Clinical Research Associate (CRA) to support monitoring and site management activities across multiple studies. The role involves close collaboration with study teams, sites, and cross-functional stakeholders, with a strong commitment to patient safety, data integrity, and product quality. Conduct on-site and remote monitoring activities , including visit preparation, follow-up, site contact, and report writing. Support site start-up activities , including EC/CA submissions, contract negotiation, and essential document collection. Schedule and conduct monitoring visits according to the study monitoring plan. Identify and report compliance issues, working with project management to ensure timely resolution. Ensure monitoring reports are finalized within 28 days of each site visit. Provide interim site management services, including remote monitoring, as required. Prior CRA experience (on-site and remote) within medical devices or pharma (ISO 14155:2020, ICH-GCP). Proactive, detail-oriented, and committed to patient safety and quality standards. ✨ This opportunity offers involvement in multiple excluively sponsor studies , exposure to a wide range of clinical operations, and the chance to work in a dynamic, high-quality environment.

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 solution

Confidencial (Prestigiosa Multinacional Europea).Gestionamos un proceso de selección para una.Multinacional Europea de primer nivel , con una sólida división de Salud y gran proyección internacional.Buscamos reforzar su estructura en España incorporando Talento directivo en Marketing para posic

INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación científica, desarrollo, fabricación, venta y comercialización de una amplia gama de principios activos farmacéuticos (API), formas farmacéuticas acabadas (FDF) y p

Scientist – Biopharma (Small & Large Molecules) Location:. A well‑established CRO operating within a GMP/GLP environment is expanding its biopharma team and seeking a Scientist to support technology transfer and validation activities across both small and large molecule products. Bachelor’s de

Insud Pharma is a recognised and respected company in the pharmaceutical and healthcare sector with more than 40 years of history and more than 7,000 employees in 50 countries specialising in the research, development, manufacture and marketing of active pharmaceutical ingredients and medicines for human and veterinary use. Chemo, industrial area of the Insud Pharma group, is a world leader in R& D and manufacturing of more than 100 value-added active pharmaceutical ingredients and more than 122 medicines with more than 200 different product presentations. Chemo produces its own active pharmaceutical ingredients (API) as well as finished pharmaceutical products (FDF) covering the main therapeutic groups (Cardiology, Gastroenterology, Central Nervous System, Anti-infectives, Respiratory, Women's Health, Endocrinology, Dermatology and Urology). General Responsibility Lead and oversee the Environmental, Health, Safety (EHS& S) strategy and operations across INSUD PHARMA's Pharma Fineshed Dosage Form (FDF) manufacturing sites (12 sites), ensuring compliance with legal requirements, corporate standards, and continuous improvement initiatives aligned with the company's strategic objectives. Specific Responsibilities Drive the reduction of safety incidents and accidents with focus on key risks (inflammables, electrical, etc.) Develop the new corporate EHS& S Master Plan 2024-2026. Define, standardize and ensure the development of corporate EHS& S policies, standards, and guidelines. Specify, harmonize and oversee the implementation of EHS& S technologies across pharmaceutical and chemical manufacturing sites. Conduct internal audits, manage corrective action plans and ensure ongoing compliance and continuous improvement. Identify, benchmark and promote best practices in safety, health, and environmental management. Lead Operational Excellence and Double Impact projects, integrating EHS& S improvements with operational and cost efficiencies. Foster a strong EHS& S culture, positioning EHS as a strategic business pillar. Manage relationships and proceedings with governmental authorities and trade union committees. Develop, monitor and report on key performance indicators (KPIs) and corporate dashboards for EHS& S performance. Oversee audits and certifications related to continuous improvement and sustainability standards (ISO14001, ISO45001, Ecovadis, PSCI). Ensure legal compliance in EHS& S and provide expert support to manufacturing locations. Requirements and personal skills Education: Degree in Engineering, Environmental Sciences, Industrial Safety or related fields. MBA will be an asset. Languages: Fluent English and Spanish. Other languages will be an asset. Experience (years/area): +10 years of proven experience in similar roles within the pharmaceutical or chemical industry. Have led HSE for a big Manufacturing site. Corporate roles and multi-site experience. Specific Knowledge: Advanced knowledge of ISO14001, ISO45001, Ecovadis and PSCI standards and certifications. Experience managing internal and external audits, KPI development and corporate dashboard tools. Travels: Available to travel once per week to the Sites in Spain (León) during the first year and then in addition once per quarter to international sites. Personal skills: Change Management Proactivity and initiative Ability to collaborate internally with production and maintenance and with with regulatory authorities and unions. Excellence organizational skills. COMMITMENT TO EQUAL OPPORTUNITIES Insud Pharma is aware that business management has to be in line with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current legislation on the subject - Organic Law 3/2007, and we do not discriminate against any person on grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

En pocas palabras Posición: Analista de Desarrollo Analítico i+D - Planta Farmacéutica Localización: Azuqueca de Henares. Experiencia: al menos 2 años en funciones similares. ¿Quieres saber más? INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación científica, desarrollo, fabricación, venta y comercialización de una amplia gama de principios activos farmacéuticos (API), formas farmacéuticas acabadas (FDF) y productos farmacéuticos de marca, con valor añadido para la salud humana y animal. La actividad de INSUD PHARMA se organiza en tres áreas de negocio sinérgicas: Industrial (Chemo), Branded (Exeltis) y Biotech (mAbxience), con más de 9.000 profesionales en más de 50 países, 20 instalaciones de última generación, 15 centros especializados de I+D, 12 oficinas comerciales y más de 35 filiales farmacéuticas, que atienden a 1.150 clientes en 96 países de todo el mundo. INSUD PHARMA cree en la innovación y el desarrollo sostenible. ¿Preparado para ser un #Challenger? ¿Qué buscamos? Incorporamos un/a Analista de Laboratorio en el área de I+D en nuestra planta ubicada en Azuqueca de Henares. ¡El reto! Análisis de materias primas y productos terminados según las Buenas Prácticas de Manufactura (GMP). Desarrollo y validación de métodos analíticos para asegurar la calidad y cumplimiento normativo. Formación y capacitación de otros analistas para garantizar altos estándares en el trabajo del laboratorio. Soporte analítico al grupo de Gálenicos, así como a los técnicos de Desarrollo Analítico y Estabilidad en I+D. Coordinación y supervisión de las tareas diarias del equipo de laboratorio para optimizar recursos y resultados. Asegurar la correcta documentación, trazabilidad y cumplimiento de normativas en todas las actividades analíticas. Participar en la mejora continua de procesos y en la resolución de incidencias técnicas. Supervisar y ejecutar análisis conforme a GMP. Gestionar la validación de métodos analíticos y asegurar su adecuada implementación. Garantizar la calidad, exactitud y trazabilidad de los análisis realizados. ¿Qué necesitas? Formación: Grado Superior en Análisis y Control de Calidad o similar. Experiencia (años/área): valorable al menos 1 año de experiencia en laboratorio farmacéutico Experiencia trabajando con HPLC, GC. Valorable manejo de Empower. Otras técnicas serán valorables Deseable: conocimientos de Software Ofimático a nivel usuario y nivel de inglés básico. Habilidades personales: buena capacidad de organización y resolución de problemas, trabajo en equipo, iniciativa y toma de decisiones. Habilidades técnicas: capacidad para trabajar en ambiente regulado ¡Nuestros beneficios! ⏰Horario rotativo de mañanas 06.00 a 14.00, tardes 14.00 a 22.00h y turno partido (flexible) Contrato indefinido Atractivo paquete salarial (salario fijo + plus rotación)

Ingeniería con importante nivel de innovación en sus proyectos, aplicando las más modernas tecnologías y en pleno proceso de expansión con clientes a nivel nacional e internacional, dedicada al diseño y fabricación llaves en mano de instalaciones para diferentes sectores industriales como el

En pocas palabras Posición: Técnico/a de Formulación Galénica de Inyectables - Contrato en prácticas Localización: Azuqueca de Henares ¿Quieres saber más INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación científica, desarrollo, fabricación, venta y comercialización de una amplia gama de principios activos farmacéuticos (API), formas farmacéuticas acabadas (FDF) y productos farmacéuticos de marca, con valor añadido para la salud humana y animal. La actividad de INSUD PHARMA se organiza en tres áreas de negocio sinérgicas: Industrial (Chemo), Branded (Exeltis) y Biotech (mAbxience), con más de 9.000 profesionales en más de 50 países, 20 instalaciones de última generación, 15 centros especializados de I+D, 12 oficinas comerciales y más de 35 filiales farmacéuticas, que atienden a 1.150 clientes en 96 países de todo el mundo. INSUD PHARMA cree en la innovación y el desarrollo sostenible. ¿Qué buscamos? Incorporamos un/a Técnico/a de Formulación Galénica de Inyectables - Contrato en prácticas para incorporarse en una de nuestras plantas ubicada en Azuqueca de Henares. Responsabilidad general Buscar y revisar bibliografía científica. Ejecutar actividades experimentales para el desarrollo y formulación de productos farmacéuticos inyectables estériles (soluciones, suspensiones, nanosuspensiones, formulaciones peptídicas, liofilizadas y 505b2). Generar y analizar datos de pruebas en cumplimiento con GMP. Apoyar en la selección y gestión de materias primas y consumibles con proveedores. Responsabilidades específicas Participar en el diseño, ejecución y supervisión de estudios de preformulación, formulación y desarrollo de procesos, así como optimización y escalado de proyectos. Realizar y documentar experimentos de desarrollo, selección de materiales y optimización de procesos de fabricación de inyectables. Apoyar la transferencia y validación de procesos a plantas GMP, colaborando estrechamente con producción y otros equipos. Contribuir a la implementación y mejora de procedimientos, plantillas y documentación interna de I+D. Resolver problemas técnicos, optimizar formulaciones y procesos, y colaborar en el análisis del desempeño técnico. Manejar equipos, realizar mantenimientos básicos, garantizar calibraciones y registrar adecuadamente los datos. Gestionar compras y relaciones con proveedores, incluyendo uso de SAP u otros sistemas en los proyectos. Redactar protocolos, informes y registros según normativas ICH y regulatorias. Participar en estudios de preformulación y formulación, incluyendo caracterización analítica básica. Buscar y analizar información relevante de bibliografía y patentes. Colaborar y mantener buenas relaciones con todos los equipos involucrados, asegurando el avance y finalización de los proyectos asignados. ¿Qué necesitas? Formación: Grado en Farmacia, Ingeniería Química, Biotecnología, Química o campo relacionado. Experiencia: valorable al menos 6 meses - 1 año de experiencia en el desempeño de las funciones descritas Idiomas: Buen nivel de inglés hablado y muy buen nivel de comunicación escrita. Se valorará el dominio del español. Estar en posesión de título de grado o máster desde hace no más de 3 años. No haber tenido anteriormente otro contrato de prácticas. Habilidades técnicas: . Conocimientos básicos sobre formas farmacéuticas y principios de formulación. . Familiaridad con técnicas y equipos de laboratorio. . Se valorará el conocimiento de las directrices GMP/GLP. Habilidades sociales: . Gran atención al detalle y capacidad para seguir instrucciones con precisión. . Buenas habilidades organizativas y de documentación. . Ganas de aprender y capacidad para trabajar eficazmente en equipo. . Actitud proactiva. ¡Nuestros beneficios! ⏰Jornada completa en horario flexible de entrada de 08:00 a 09:30h y salida en función de la hora de entrada desde las 16:30h &##128220;Contrato formativo para la obtención de la práctica profesional por 6 meses y posibilidad de ampliar hasta 12 &##128184;Salario según mercado &##129404; Seguro de vida y accidentes. &##129404; Copago en el seguro voluntario de salud. &##128184;Club de Beneficios y Ahorro. &##128200;Planes de desarrollo, política de movilidad interna. ⭐¡Muchos más! ¿Cómo será el proceso de Selección? &##128373;️ ➡️¡Estate atento/a al teléfono y al correo! Seguramente lo primero que haremos será contactarte por alguna de las dos vías. ➡️¡Prepárate bien! Continuaremos con una entrevista presencial/virtual según la disponibilidad y acordemos, en el proceso puede haber entre una y dos entrevistas y según el tipo de proceso puede haber también algún tipo de prueba. ➡️¡Espera el resultado! Nos preocupamos de que cada proceso de selección os sintáis guiados y sabiendo qué esperar de nosotros, por lo que procuraremos indicaros siempre el estado del proceso. &##128311;¿Crees que esta oferta no es para ti? &##128311; Síguenos en redes sociales como LinkedIn/Instagram y estate atento a cualquier oferta que vayamos sacando, ¡La oportunidad de ser un nuevo Insuder está a la espera!. #InsudPharma #Challenger #Insuder #InsudTalent COMPROMISO CON LA IGUALDAD DE OPORTUNIDADES El grupo InsudPharma es consciente que la gestión empresarial tiene que estar en consonancia con las necesidades y demandas de la sociedad, y por ello asume el compromiso de igualdad de oportunidades y trato entre hombres y mujeres, tal y como se recoge en la normativa vigente en la materia -Ley Orgánica 3/2007, y no discriminamos a ninguna persona por motivos de etnia, religión, edad, sexo, nacionalidad, estado civil, orientación afectiva o sexual, identidad o expresión de género, discapacidad, o cualquier otra circunstancia personal o social.

A dynamic, supportive team committed to innovation and patient access Exposure to diverse therapeutic areas and cutting‑edge digital health technologies Competitive salary and benefits package Professional development in a rapidly evolving area of clinical operations About Planet Pharma:. Planet P

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissio

A leading pharmaceutical company in Barcelona is seeking a Head of Marketing with 8-12 years of pharmaceutical marketing experience, ideally in Specialty Care. The role involves defining the marketing strategy, leading brand initiatives, driving launches, and fostering team development.

Candidates should have over 15 years of supply chain experience, ideally in the health or cosmetic industry, along with a degree in relevant fields. The role requires strong leadership and a proactive approach to improving supply chain processes. A leading dermatology company is seeking a Global Hea

About the Role We are seeking a visionary and experienced supply chain leader to join Galderma as Global Head of ESO Supply Chain. You will oversee supply chain processes for the global supply relationship teams (SRTs), drive process improvements, and foster collaboration across affiliates, sites, a

A leading pharmaceutical company is seeking a Global Head of Demand Planning in Barcelona. This role demands at least 5-7 years of experience in demand planning within the pharmaceutical or consumer health sectors, excellent leadership abilities, and fluency in Spanish and English.

A growing pharmaceutical company in Madrid is seeking an experienced Operations Director to own production and packaging at an expanding site. The ideal candidate will have a strong background in pharma operations, change management, and be fluent in both Spanish and English.

Una empresa líder en analítica de datos busca un profesional experimentado para diseñar y implementar soluciones analíticas en el sector Pharma.

This pivotal role emphasizes leveraging data to identify commercial opportunities and translating insights into strategies with a focus on SaaS and pharma.

A leading pharmaceutical manufacturer in Spain is seeking a Head of Global Engineering. This strategic role will oversee engineering excellence across multiple manufacturing sites worldwide, requiring over 15 years of experience in API and Pharma engineering, along with proven abilities in managing

Additional degree in Clinical Pharmacology and/or Pharmacovigilance/Drug. Safety and/or Public Health and/or epidemiology, preferred* 12 years of global experience in Drug Development, Clinical Safety, or Pharmacovigilance in a global pharmaceutical company in a matrix organization is required*

Candidates must possess a relevant University Degree and at least 2 years of experience in validations or quality systems within the pharmaceutical industry.

A leading global dermatology company seeks a Global Executive Search Partner to manage the full executive search process.The ideal candidate will have experience in talent acquisition, a solid network in executive-level recruitment, and a strong ability to work collaboratively across international m

Una consultora de recursos humanos busca un/a HR Business Partner para una compañía farmacéutica en Barcelona.Con un contrato temporal por sustitución de maternidad y modalidad de trabajo flexible, este rol ofrece la oportunidad de formar parte de un entorno internacional y dinámico.Se requiere

Una agencia de comunicación en salud busca un Director/a de Cuentas para liderar la gestión de cuentas clave en el sector farmacéutico.El candidato ideal tendrá más de 4 años de experiencia en agencia y habilidades de liderazgo en entornos dinámicos.Dominio del inglés y capacidad para diseñ

Únete a nuestro equipo como Agente de Telemarketing.Te apasiona la comunicación y el trato con el cliente? ¿Te gustaría formar parte de un proyecto con una de las compañías farmacéuticas más reconocidas del sector? Buscamos un/a agente de Telemarketing para dar soporte a un laboratorio l�

Our mission is to improve global health by optimizing how medicines are manufactured so that pharma and biotech companies can provide patients worldwide with the right medicine at the right time and price. The Junior EBR Consultant will inspire our customers through technology, using his/her growing

A leading pharmaceutical company in Girona, Spain is seeking a Head of Legal to lead the legal department and oversee its operations.The role requires at least 10-15 years of experience in legal roles within the pharmaceutical sector, strong skills in corporate law, and the ability to provide strate

The ideal candidate has over 10 years of experience in the pharmaceutical sector, with proven leadership skills and a robust understanding of GxP compliance.

A technology consulting firm in Spain is seeking an experienced backend software engineer to build a centralized testing platform for the pharmaceutical sector.

A global dermatology leader is seeking a Global Executive Search Partner focused on identifying executive talent across international markets.The role entails managing the entire executive search process, engaging with high-level candidates, and providing advice to hiring managers.Ideal candidates w

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissio

Ideal candidates should have 8-10 years of brand management experience in the pharmaceutical industry, excellent communication skills, and fluency in both Spanish and English. A leading pharmaceutical company is seeking a Senior Brand Manager for its Consumer Health segment in Barcelona, Spain.

A leading dermatology company in Barcelona seeks a Global Talent Acquisition Lead to design and implement talent acquisition strategies for manufacturing operations.The role demands collaboration with business leaders to ensure a high-performing workforce and champion Diversity, Equity, and Inclusio

With offices in Barcelona, the UK, and China, we provide unparalleled support to global Pharmaceutical, Biotech, and Medical Device supply chains. To stand out, please send a motivation letter explaining why you are interested in Rephine, which QMS systems or software you have implemented, and your

A leading pharmaceutical company in Barcelona is seeking a Strategy Senior Manager to support strategic decision-making and drive execution of key initiatives. The ideal candidate will have a scientific degree combined with a Master’s in Business and experience in Strategic Consulting or the Pharm

A leading pharmaceutical company located in Barcelona is seeking an AI Solutions Senior Architect to lead the design and integration of generative AI solutions across its digital ecosystem.

Acerca de Exceltic Exceltic es una empresa de ingeniería y consultoría tecnológica con más de 600 profesionales, presencia en 5 continentes y proyectos en sectores como energía, pharma, defensa, automoción, ferroviario, telecomunicaciones y banca. En Exceltic estamos buscando un/a Data Analyst

Solid academic background or professional experience in Data Science, Machine Learning, Statistics, or a related quantitative field Strong experience working with time series data from sensors or monitoring devices Advanced Python proficiency and experience with common data science libraries Applied

Ideal candidates should have over 15 years of experience in supply chain management, preferably in the health or pharmaceutical industry, along with a strong academic background and leadership qualifications.

Global Talent Acquisition Lead – Manufacturing & Industrial Operations page is loaded## Global Talent Acquisition Lead – Manufacturing & Industrial Operationslocations:.Posted Todayjob requisition id:.JR016928Galderma is the emerging pure-play dermatology category leader, present in approximatel

Un importante laboratorio farmacéutico en Barcelona busca un Regulatory Affairs Manager para liderar las actividades regulatorias y garantizar el cumplimiento normativo.El candidato ideal debe tener más de 5 años de experiencia en asuntos regulatorios, conocimiento profundo de normativas nacional

Managing the compliance network across EMEAC and coordinating activities, including working closely with each Country Compliance Officer and, where no CCO exists in a country, the relevant Compliance Liaison in such country or, in the case of Europe Middle Markets (EMM), the EMM Compliance Liaison.

Educational qualification : Bachelors degree in Marketing Business Pharmacy or Life Sciences (Masters preferred). Minimum work experience : Minimum 8-10 years of experience in brand management within the pharmaceutical / consumer health industry (on OTC medicine).

A global pharmaceutical company based in Barcelona, Spain, is seeking an Associate Director IT Solution Architect to lead the architecture of a next-generation Statistical Compute Environment.

Una consultora de selección busca un/a Director/a de desarrollo de negocio en el sector farma para una importante empresa internacional.El candidato ideal tendrá pasión por las ventas y la capacidad de desarrollar una cartera de clientes.Las responsabilidades incluyen la prospección comercial y