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La actividad de INSUD PHARMA se organiza en tres áreas de negocio sinérgicas: Industrial (Chemo), Branded (Exeltis) y Biotech (mAbxience), con más de 9.

Drasanvi es una empresa española experta en salud natural y nutrición desde 1993.Líder en el mercado del colágeno y una de las principales marcas de salud y belleza natural,.Drasanvi (España), EA Pharma (Francia), Stardea (Italia) y W Group (Estados Unidos), además de 4 marcas globales: Drasan

Posición: Técnico/a en Relaciones Laborales - Contrato Temporal Experiencia: al menos 3-4 años en el desarrollo de funciones comentadas INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación científica, desarrollo, fabr

Experiencia a partir de 5 años en departamento producción industrial preferiblemente en sectores regulados, como el de Medical Devices, Pharma, Laboratorios.

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

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. LETI Pharma promueve el desarrollo profesional y personal de todas las personas colaboradoras, asegurando la ig

This role will be key in driving commercial expansion within pharmaceutical, biotech, and CRO environments, supporting clinical trials and precision medicine strategies on a global scale. Identify, engage, and develop relationships with pharma, biotech, and CRO partners across Europe, the US, and ot

Perform clinical trial-related procedures including blood sampling and injections ECG performance (recording only; Qualified nurse with a minimum of 3 years post-registration experience Previous clinical trial experience strongly preferred Valid and current GCP certificate (R3) — candidates in pro

Want to know more? INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and

You’ve gained experience in a pharmaceutical Gx P environment (Engineering, Maintenance, Validations, Production, or Quality Assurance). You’re eager to learn, motivated, and passionate about Pharma Consulting. With offices in Barcelona, the UK, India, and China, we proudly support Pharmaceutica

Position: Finance Senior Analyst INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a broad range of active pharmaceutical ingredients (API), finished dosage fo

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. LETI Pharma promueve el

With offices in Barcelona, the UK, India, and China, we proudly support Pharmaceutical, Biotech, and Medical Device supply chains across the globe. Are you passionate about Pharma and Life Sciences? Do you thrive in dynamic team environments and enjoy traveling for impactful projects? If you're read

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. LETI Pharma promueve el desarrollo profesional y personal de todas las personas colaboradoras, asegurando la ig

Scope of the Role 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 line with corporate priorities across neurology, rare diseases, women's health, and specialty care. The position offers high cross-functional visibility and direct interaction with external partners, senior leadership, and internal decision forums reporting to Director, Business & Portfolio Development. Key Responsibilities: Opportunity identification & evaluation Perform structured scouting of external assets, platforms, technologies, and companies aligned with ITF's strategic priorities. Conduct commercial, scientific, regulatory, and competitive assessments to support go/no-go decisions. Build and refine financial models (NPV, r NPV, P& L impact, scenario analyses). Deal process management Lead the full lifecycle of BD processes: screening → non-confidential evaluation → due diligence → term sheet negotiation → contract execution. Coordinate internal cross-functional teams (Medical, Clinical, Regulatory, CMC, Supply Chain, Finance, Legal). Prepare materials for internal governance committees (NPC, Board, investment committees). Partner interface & relationship building Serve as the point of contact for external companies, advisors, and investors during evaluations and negotiations. Represent Italfarmaco at partnering conferences, scientific congresses, and industry events. Build and maintain a proactive external network to support deal sourcing. Strategic contributions Monitor industry trends, competitive landscapes, and potential shifts in therapeutic and regulatory environments. Provide insights that help shape ITF's long-term portfolio and BD sourcing roadmap. Operational excellence Ensure high-quality documentation, timelines, and project management across all BD processes. Guarantee confidentiality and rigorous data-handling standards throughout due diligence. Level-Specific Responsibilities: Drive workstreams within broader BD projects under the supervision of a Senior Manager or Director. Conduct first-pass commercial and competitive evaluations and prepare internal recommendation documents. Support financial modelling and cross-functional assessments. Assist in drafting and reviewing term sheets and contract language in coordination with Legal. Coordinate specific components of due diligence and maintain tracking tools, timelines, and documentation. Requirements: Experience Minimum 5+ years in pharma, biotech, consulting, licensing, or R& D strategy roles. Education & Qualifications Advanced degree (Life Sciences, Pharmacy, Medicine, Biotechnology). MBA strongly preferred; alternatively, a Ph D in Life Sciences is valued. Solid understanding of drug development, regulatory pathways, lifecycle management, and commercial dynamics. Skills & Competencies Strong analytical and strategic thinking, with ability to translate scientific and commercial information into actionable recommendations. Experience with term sheets, deal structures, licensing frameworks, and collaboration models. Ability to lead and coordinate cross-functional teams in fast-paced, multitasking environments. Excellent communication and relationship-building skills across external stakeholders and internal teams. High proficiency in business English; working knowledge of Italian or Spanish is an advantage. Strong project-management discipline, attention to detail, and ability to manage several evaluations simultaneously. Willingness to travel internationally (~20–30%).

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

Pharmaceutical Development Manager - External Operations Experience: More than 5 years in the development of the position and duties described INSUD PHARMA operates across the entire pharmaceutical value chain, providing expertise and experience in scientific research, development, manufacturing, sales and marketing of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDFs) and branded pharmaceutical products, with added value for human and animal health. INSUD PHARMA's activity is organised into three synergistic business areas: Industrial (Chemo), Branded (Exeltis) and Biotech (mAbxience), with more than 9,000 professionals in over 50 countries, 20 state-of-the-art facilities, 15 specialised R&D centres, 12 commercial offices and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries around the world. INSUD PHARMA believes in innovation and sustainable development. We are recruiting a Pharmaceutical Development Manager – External Operations to join the R&D team at one of our plants located in Azuqueca de Henares. As Pharmaceutical Development Manager - External Operations, you will lead, coordinate and supervise pharmaceutical development projects carried out at Insud Pharma Group's sites outside Spain and with external partners. Your mission: to ensure the highest quality development and smooth technology transfer of solid oral and semi-solid dosage forms from external centres to our flagship plant in Spain, driving the success of the portfolio in multiple markets. Provide strategic oversight of R&D projects developed at Insud Pharma Group plants outside Spain and through external partners such as CDMOs worldwide, primarily in solid oral and semi-solid dosage forms. ~ Manage all formulation, analytical and process development activities, from pre-formulation to industrialisation, ensuring overall compliance with corporate objectives, regulatory requirements and project deadlines. ~ Supervise, guide and inspire a high-performance team; Review, approve and validate project documentation (development, analytical, regulatory, clinical) prepared by international and third-party teams, ensuring the most rigorous standards for regulatory submission and audit readiness. ~ Drive seamless technology transfer and product scaling, ensuring robust implementation in Spanish production (Liconsa), including plant preparation, process reproducibility, equipment qualification and comprehensive technical documentation. ~ Align projects and coordinate effectively with global cross-functional teams: Clinical Development, Production, Regulatory Affairs, Business Development, Supply Chain, Quality, among others. ~ Propose optimal resource allocation and lead change initiatives to enhance capacity, efficiency and adoption of best practices in internal and external networks. ~ Monitor KPIs for deadline compliance, document quality, process reproducibility and submission/approval rates; proactively address project risks and leverage new opportunities. ~ Present project status and strategic recommendations to senior management and global leadership, acting as a visible benchmark for external innovation, excellence, and patient-centred value. ~ Support business audits, budget planning, and talent development; play a key role in organisational and cultural integration. Higher degree in Pharmacy, Pharmaceutical Sciences, Chemistry or related field. ~≥5 years of experience in pharmaceutical development, with proven experience in managing international projects and with third parties (/CDMOs); experience in generic drug development highly valued. ~ Solid knowledge of formulation, analytical and process development—especially for solid and semi-solid oral forms; Fluency in English (spoken/written); Spanish and/or other languages will be a significant advantage. ~ Excellent project management, negotiation, and interpersonal skills; proven track record in problem solving, innovation, and meeting objectives on time and within budget. ~ Passion for quality, patient safety, and making a difference in global health. Monday to Friday working hours, with flexible start times between 8:00 a.m. Permanent contract.

Perform clinical trial-related procedures including blood sampling and injections ECG performance (recording only; Qualified nurse with a minimum of 3 years post-registration experience Previous clinical trial experience strongly preferred Valid and current GCP certificate (R3) — candidates in pro

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

✨ Acerca de la empresa: Vincle, consultora tecnológica especializada en el proceso comercial con más de 30 años de experiencia en los sectores del Gran Consumo y Pharma con proyectos a nivel internacional. La innovación es uno de nuestros pilares fundamentales, por lo que nuestra plataforma y nuestro equipo están en constante evolución para estar a la vanguardia de la tecnología y los procesos que cubrirán las próximas necesidades que requiera el mercado. ¿ Quieres conocer más? Entra en nuestra web: . Sobre el Rol: Queremos hacer crecer nuestro equipo de desarrollo de producto con un/a Back End Developer - Spring & Microservices y así poder asumir más retos tecnológicos y guiar en el avance del producto. Te detallamos nuestro stack tecnológico: Java Spring Framework Micorservicios Cassandra Elasticsearch Docker Kubernetes Rabbit MQ SQL Mongo DB Azure cloud platform Git Responsabilidades: Será responsable del desarrollo de nuevas funcionalidades y/o personalizaciones en las diferentes plataformas con las que trabaja la compañía, a partir de los análisis técnicos realizados. Participará activamente en la toma de requerimientos y será responsable de realizar análisis técnicos y funcionales de nuevas funcionalidades, así como de dar soporte sobre las existentes. Ayudará y guiará al equipo de Developers en el uso de métodos, técnicas y herramientas adecuadas para el desarrollo del trabajo colectivo. Cualificaciones: Ingeniería Informática o similar. Habilidades Requeridas: Experiencia de más de 5 años en programación con Java Spring y mínimo 3 con microservicios. Git tiene que ser tu día a día. Tener experiencia en trabajar bajo metodologías Scrum. Experiencia con Docker y / o Kubernetes. Experiencia en base de datos no relacionales. Buenas prácticas de desarrollo (Clean code, Yagni, Kiss..). Patrones de diseño. Experiencia en el desarrollo impulsado por pruebas y los marcos de pruebas unitarias. Conocimiento sobre servicios basados en la nube (computación sin servidor, bus de mensajes, bases de datos, etc.) preferiblemente con Azure Cloud. Condiciones: Modelo híbrido oficina-remoto: 3 de oficina (Barcelona ciudad, Pozuelo de Alarcón-Madrid o Cádiz) y 2 días a la semana de teletrabajo. Flexibilidad horaria de entrada y salida. Contrato indefinido. Jornada intensiva viernes y en verano (Julio y Agosto). 23 días de vacaciones. Actividades de equipo y afterwork. Formación activa dentro de la empresa. A partir de los 6 meses retribución flexible de plan de seguro médico. Nuestros valores: Team players: Lo más importante son las personas. Juntos llegamos mucho más lejos. La comunicación y el trabajo en equipo nuestros pilares para conseguirlo. Make things happen: conseguimos llevar las ideas a la realidad. There is no limit: Nos marcamos metas ambiciosas, tenemos curiosidad y no tenemos miedo al fracaso. Si tienes techo, rómpelo! Passionate players: Trabajamos con actitud positiva y ponemos pasión en todo lo que hacemos. ¿ Quieres divertirte construyendo una plataforma que cambiará el modo de ver las ventas? Ven a un equipo donde se transmite el buen rollo y no nos asusta ningún reto! ¿ A qué estás esperando para unirte?

¿Te interesaría seguir desarrollándote como QA Validation & Qualification Specialist en una multinacional líder del sector farmacéutico, participando en la mejora continua de sus plantas productivas y colaborando con equipos técnicos multidisciplinares? Desde Oxigent Technologies seleccionamos un/a QA VALIDATION & QUALIFICATION SPECIALIST para incorporarse en una compañía multinacional, ubicada en San Sebastian de los Reyes, Madrid. ¿Cuáles serán tus funciones principales? Realización de validaciones de proceso y de limpieza: • Planificación, ejecución y documentación de estudios de validación para asegurar que los procesos productivos y los procedimientos de limpieza cumplen con los estándares internos y regulatorios. Evaluación de riesgos, definición de criterios de aceptación, seguimiento de resultados y elaboración de informes técnicos conforme a GMP. Aplicación y supervisión de prácticas asépticas: • Implementación y verificación del cumplimiento de las prácticas asépticas en entornos de producción estéril. Formación del personal, monitorización del comportamiento en áreas clasificadas, investigación de desviaciones y propuesta de acciones correctivas/preventivas (CAPA). Conocimiento y ejecución de actividades relacionadas con media fill: • Planificación, coordinación y supervisión de simulaciones de llenado aséptico (media fill) según la normativa vigente. Revisión de protocolos, control de las condiciones de ejecución, análisis de resultados y preparación de la documentación requerida para garantizar el estado de control del proceso. Cualificación de equipos de envasado (OQ y etapas relacionadas): • Participación en las fases de cualificación de equipos (DQ, IQ, OQ y soporte en PQ) para líneas de envasado estéril. Revisión de URS, elaboración y ejecución de protocolos, verificación del cumplimiento de especificaciones técnicas, análisis de desviaciones y generación de informes finales. Colaboración transversal con Producción, Calidad e Ingeniería: • Apoyo técnico en la implementación de mejoras de proceso, gestión de cambios, resolución de desviaciones y optimización del rendimiento de las líneas, asegurando siempre el cumplimiento de las GMP y los estándares regulatorios. Para ello, ¿qué vas a necesitar? • Formación: Ingeniería Industrial, Mecánica, Eléctrica o similar. • Mínimo 3 años gestionando proyectos similares, con conocimiento de clean utilities, normativa GMP y conocimiento de inyectables y estériles. • Nivel conversacional de Ingles (B2+) ¿Qué te ofrecemos? • Contratación indefinida a través de Oxigent. • Salario acorde a la experiencia aportada (entre 45.000 - 55.000 euros brutos anuales) • Horario flexible • Modelo presencial • Cheque Formación para desarrollarte en las áreas profesionales que más te interesen. • Seguro médico privado. • Retribución flexible aplicable a seguro médico, restaurante, transporte, guardería y formación. • Aplicación de acceso a gimnasios y actividades deportivas en toda España con descuentos. • ¡Y muchos otros beneficios! ¡Únete al equipo de Oxigent! Empresa comprometida con la sostenibilidad y la igualdad de oportunidades, donde el talento y la tecnología no entienden de género.

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)

La actividad de INSUD PHARMA se organiza en tres áreas de negocio sinérgicas: Industrial (Chemo), Branded (Exeltis) y Biotech (mAbxience), con más de 9.

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

In a nutshell Position: Commercial Controller Location: Madrid Experience: Minimum 4 years in similar roles Want to know more? INSUD PHARMA operates across the entire pharmaceutical value chain, bringing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health. INSUD PHARMA is continuously growing and is looking for a Commercial Controller to join its finance team and support decision-making that improves the company's financial performance. Ready to be a #Challenger? What are we looking for? Collaborate with commercial teams to provide financial reviews, variance analysis, and strategic insights that drive profitability and informed decision-making. Lead monthly revenue reporting and profitability tracking, ensuring accuracy and transparency across products, customers, and geographies. Deliver ad-hoc analysis for business cases, investments, pricing decisions, and product launches, supporting commercial strategy with robust financial modeling. Support the Sales & Operations Planning (S& OP) process by validating financial inputs, ensuring reliability of estimates, and tracking performance against targets. Manage month-end revenue closing and consolidation for internal and HQ reporting, leveraging advanced Excel and automation tools (Power Query, VBA, Power Pivot, Power Automate). Liaise with cross-functional teams to ensure ERP and Power BI data accuracy, troubleshoot issues, and support continuous improvement of financial systems. The challenge! Supervise, analyze, coordinate, report, automate, and collaborate to maximize financial efficiency and support INSUD PHARMA's commercial strategy. What do you need? Bachelor's degree in Finance, Business Administration, Accounting, or related field. Minimum 4 years' experience as a Business Controller or Commercial Controller, preferably in industrial or manufacturing environments. Proven expertise in profitability analysis, gross-to-net calculations, and working across multi-currency international markets. Strong knowledge of financial statements, budgeting, and forecasting processes. Postgraduate qualifications (MBA, Master's in Finance) and/or professional certifications (CFA, CPA, CIMA) highly valued. Advanced proficiency in Microsoft Excel and automation tools (Power Query, VBA, Power Pivot, Power Automate). Experience with SAP platforms (Business Objects, BPC, Analytics Cloud) and Power BI is a plus. Full professional proficiency in English; Spanish is a plus. Exceptional analytical skills, commercial acumen, and ability to work independently and collaboratively in multicultural, cross-functional teams. Our benefits! Permanent contract Flexible working hours Private health insurance Professional development and continuous training Growth opportunities within INSUD PHARMA How will the selection process be? ️ Initial contact by phone or email. 1 or 2 virtual or onsite interviews with HR and the finance team. Constant communication about the status of the process. Think this offer is not for you? Follow us on Linked In and Instagram for more job opportunities. Don't miss the chance to be part of INSUD PHARMA! #Insud Pharma #Challenger #Insuder #Insud Talent COMMITMENT TO EQUAL OPPORTUNITIES At INSUD PHARMA, we promote gender equality and guarantee an inclusive work environment free from discrimination based on ethnicity, religion, sexual orientation, disability, or any other personal or social condition.

Perform clinical trial-related procedures including blood sampling and injections ECG performance (recording only; Qualified nurse with a minimum of 3 years post-registration experience Previous clinical trial experience strongly preferred Valid and current GCP certificate (R3) — candidates in pro

Perform clinical trial-related procedures including blood sampling and injections ECG performance (recording only; Qualified nurse with a minimum of 3 years post-registration experience Previous clinical trial experience strongly preferred Valid and current GCP certificate (R3) — candidates in pro

From Temporing Barcelona we select a Talent Acquisition Specialist (Pharma) for an important company in the pharmaceutical sector located in Sant Joan Despí. Possibility of working in a leading company in the pharmaceutical sector.

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

Con sede central en Barcelona, y planta productiva y laboratorio de investigación en Madrid, contamos también con filiales en Alemania y Portugal. Su misión será garantizar la seguridad y salud de todas las personas en la organización, mediante la identificación, evaluación y control de riesg

Posición: Operarios/as de fabricación/formulación de inyectables - Zona estéril Localización: Azuqueca de Henares Experiencia: al menos 1 año en funciones similares.INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigaci�

This role will be key in driving commercial expansion within pharmaceutical, biotech, and CRO environments, supporting clinical trials and precision medicine strategies on a global scale. Identify, engage, and develop relationships with pharma, biotech, and CRO partners across Europe, the US, and ot

This role will be key in driving commercial expansion within pharmaceutical, biotech, and CRO environments, supporting clinical trials and precision medicine strategies on a global scale. Identify, engage, and develop relationships with pharma, biotech, and CRO partners across Europe, the US, and ot

Buscamos un/a Investigador/a de I+D con experiencia en Entomología y conocimiento profundo en biología de artrópodos.

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

Posición: Continuous Improvement Trainee Localización: Azuqueca de Henares.Experiencia: No es necesaria, tienes que haber terminado la carrera hace menos de 3 años y no haber hecho ningún contrato formativo para la obtención de la práctica profesional.INSUD PHARMA opera en toda la cadena de va

Únete a Naos como Vendedor Especializado en Cuidado de la Piel para Farmacias! Estamos buscando un delegado de farmacia para las zonas de Pontevedra, Ourense y sur de A Coruña.Trabajarás dos grandes marcas: Bioderma e Institut Esthederm.Tu misión principal será contribuir a los resultados de la

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 degree in Chemistry, Biochemistry, Biotechnology, or a related

La actividad de INSUD PHARMA se organiza en tres áreas de negocio sinérgicas: Industrial (Chemo), Branded (Exeltis) y Biotech (mAbxience), con más de 9.

Experiencia a partir de 5 años en departamento producción industrial preferiblemente en sectores regulados, como el de Medical Devices, Pharma, Laboratorios.

Want to know more? INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a broad range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and

Oxford Global Resources Consulting has an opening role for initial 6 months for an International Customer Service position in Barcelona Logistics and Export (International Sales).This role is a 6 months project with our client, top leading HQ Pharma Company located in Barcelona.Oxford Global Resourc

We are seeking experienced freelance Clinical Research Nurses to support an Acute Ischaemic Stroke study.

Sobre BWT En BWT Pharma & Biotech Ibérica, perteneciente al grupo internacional BWT – Best Water Technology, somos líderes en el diseño, fabricación e instalación de sistemas de tratamiento de aguas y clean utilities para la industria farmacéutica y biotecnológica. Cómo postular Si tienes

Position: Finance Senior Analyst INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a broad range of active pharmaceutical ingredients (API), finished dosage fo

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.

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