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Environmental Health and Safety (EHS) Risk Management, Environment Health and Safety, Health and Safety Legislation, Health Safety (Inactive), Health Safety and Environment (HSE) Management Systems, Health Safety Regulations, Regulatory Compliance, Risk Prevention. En el centro de todo lo que hacemo

🛰️ Indra Space – Leading the Next Generation of Space Systems 🌌 At Indra Space, we are on a mission to redefine the European space industry by delivering high-performance small satellite solutions for LEO missions. Our ambition? To become a leading company in end-to-end satellite systems, driving innovation in: • Position, Navigation & Timing (PNT), • Secure Communications, • Earth Observation & ISR, • Space Domain Awareness (SDA) and Space Traffic Management (STM), • Science & space exploration As the Space Business Unit of Indra Group, we combine cutting-edge technology with a full value chain approach—from satellite design and integration to ground segment and operations. With the integration of Deimos and strategic participation in Hispasat and Hisdesat, we are scaling Europe’s space autonomy and contributing to flagship programs like IRIS², Galileo, EGNOS, and Copernicus. 💡 What will you do? • Define and lead the satellite power and data distribution architecture, including interface boards, umbilicals, power distribution units and conversion electronics., • Translate mission requirements into power and data distribution concepts, grounding strategies and EMC performance criteria., • Lead trade-off analyses between architectures such as point-to-point, backplane or direct connection approaches., • Generate and maintain electrical, grounding, EMC, harness requirements, EICDs, and subsystem interface specifications., • Develop power budgets, energy balance analysis and end-of-life sizing for different mission scenarios., • Ensure compliance with mission reliability, redundancy and derating standards., • Coordinate harness procurement and development with internal teams and external suppliers., • Support AIT activities including functional, thermal vacuum and load test campaigns., • Act as technical authority during project reviews (PDR, CDR, TRR, FRR)., • Collaborate with mechanical, thermal, software, V&V and systems teams to define system-level specifications., • Provide mentorship and technical guidance to junior engineers., • Prepare system specifications, design reports, test plans and other technical documentation., • Work closely with procurement to provide technical assessment of supplied items., • Stay up to date with advancements in avionics, satellite design and space technologies to support innovation. 🎯 What are we looking for? • A recognized engineering degree in Mechanical, Aerospace, Electrical, Electronic Engineering or related fields., • Minimum 5 years of experience in satellite electrical design and development, including flight projects., • Strong knowledge of spacecraft solar arrays, battery technologies and power electronics., • Experience with regulated and unregulated power buses and peak power tracking., • Familiarity with industry standards (ECSS, MIL-STD, NASA)., • Proficiency with system analysis tools such as MATLAB, Simulink or Altium., • Proven experience leading system design across the full lifecycle (concept to launch)., • Experience in aeronautical/aerospace electrical architecture., • Familiarity with AIT campaigns for satellites and/or launchers., • Experience with EGSE and satellite test environments in phases C/D., • Strong problem-solving skills and ability to coordinate across multidisciplinary engineering domains., • Excellent communication and leadership skills., • High-level English (spoken and written)., • Availability to work in a hybrid model in Madrid. Don’t worry if you don’t meet 100% of the requirements. Apply, learn about our proposal, and show us what you can bring! 🚀 What we offer • Work Your Way: Flexible hours so you can balance life and work effortlessly., • Open Culture: Direct communication and a friendly environment where your voice matters., • Innovation at Its Core: Be part of groundbreaking projects with global impact., • People First: A collaborative team that supports and celebrates your success., • Career Acceleration: Continuous feedback and annual reviews to help you grow., • Stability You Can Trust: Long-term projects in a leading company with a future vision., • Global Reach: Your work will influence major international initiatives., • Mobility Opportunities: Explore projects across Spain and beyond., • Lifelong Learning: Access Open University programs and 3,000+ Udemy for Business courses. ✨ Your next big opportunity is here. Ready to make an impact? Apply today!

Planet Pharma are currently partnered with a global pharma and we are actively seeking a Clinical Research Nurse in Albacete to join the business.Coordinate and conduct clinical research studies in compliance with protocols, GCP (Good Clinical Practice), and regulatory requirements.Recruit, screen,

Position: Clinical Research Associate Location: Azuqueca de Henares. Experience: 2 to 4 years in similar roles. Do you want to know more?👇 INSUD PHARMA operates throughout 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 branded pharmaceutical products, adding value to both human and animal health. INSUD PHARMA’s activity is structured 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 specialized R&D centers, 12 commercial offices, and over 35 pharmaceutical subsidiaries, serving 1,150 clients in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Are you ready to be a #Challenger? The challenge! • Collaborate with Clinical Development Leaders to execute assigned trials aligned with the product development plan., • Take ownership of trial execution, reporting, and evaluation, ensuring compliance with GCP and applicable regulations., • Support clinical trial activities according to ICH/EMA/FDA and other relevant guidelines., • Participate in the selection of CROs and external vendors; oversee contracted activities (cost, quality, timelines)., • Review key trial documentation (e.g., Protocol, ICF, monitoring oversight, study report)., • Work closely with sponsor teams, CROs, and site staff in multidisciplinary environments., • Oversee monitoring documentation (e.g., MVRs), SDV quality, and site readiness/compliance., • Oversee training of site staff on protocols, safety reporting, and GCP., • Oversee IP handling, storage, and accountability at sites., • Proactively identify risks and drive corrective and preventive actions (CAPA)., • Coordinate internal CHEMO activities linked to trial conduct (e.g., investigational product shipments)., • Partner with cross-functional teams (Pharm Dev, Regulatory, PV, Project Management) to support execution., • Contribute to GCP system maintenance through SOP development/review. What do you need? • University degree in a Life Sciences discipline (mandatory), • 2+ years in a similar CRA/clinical trial oversight role, • Experience in global clinical development and trial implementation (site selection/management, monitoring activities), • Remote and on-site monitoring exposure, including risk-based monitoring (RBM), • Strong understanding of ICH-GCP, FDA, EMA, and local regulatory requirements, • Skilled in identifying/documenting/escalating AEs/SAEs, • Experience preparing and reviewing study documentation, • Fluent English required, • Strong cross-functional collaboration in international settings, • Proactive, hands-on, “can-do” mindset with strong ownership, • Excellent organization, attention to detail, communication, and time management, • Comfortable with Microsoft Office for reporting/documentation, • Sound judgment, curiosity, and willingness to learn Our benefits! ⏰Flexible entry schedule from Monday to Friday (full-time, 40 hours). 📜Permanent contract 💸Attractive salary package. 🥼 Life and accident insurance. 🍽️ Company cafeteria (free). 🥼 Co-payment on voluntary health insurance. 💸Benefits & Savings Club. 📈Development plans, internal mobility policy. ⭐And many more! How will the selection process be? 🕵️ ➡️Stay alert to your phone and email! Most likely, the first thing we will do is contact you through one of these channels. ➡️Get ready! We will continue with an in-person/virtual interview depending on availability and as we agree; the process may include one or two interviews, and depending on the type of process, there may also be some sort of test. ➡️Wait for the result! We care that in each selection process you feel guided and know what to expect from us, so we will try to inform you about the status of the process at all times. 🔷Do you think this offer is not for you?🔷 Follow us on social media like LinkedIn/Instagram and stay tuned for any openings we post: the opportunity to become a new Insuder is waiting! #InsudPharma #Challenger #Insuder #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must be in harmony with the needs and demands of society, and therefore undertakes a commitment to equal opportunity and treatment between men and women, as set out in current regulations—Organic Law 3/2007—and we do not discriminate against anyone based on ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

Position: Pharmacometrician Scientist Location: Azuqueca de Henares. Experience: 2 to 4 years in similar roles. Do you want to know more?👇 INSUD PHARMA operates throughout 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 branded pharmaceutical products, adding value to both human and animal health. INSUD PHARMA’s activity is structured 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 specialized R&D centers, 12 commercial offices, and over 35 pharmaceutical subsidiaries, serving 1,150 clients in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Are you ready to be a #Challenger? What are we looking for? 🔎 The challenge! • Provide technical and scientific support for NME and complex generic development projects, driving appropriate biopharmaceutical assessment and contributing to the selection of formulation prototypes., • Identify relationships between drug substance properties, dosage forms, drug release, and drug absorption., • Build mathematical models describing formulation effects on drug absorption (IVIVC and PBPK models)., • Develop predictive PK models based on in vitro dissolution data (IVIVC)., • In collaboration with other team members, develop PK/PD models to address questions related to complex generic products., • Contribute to the implementation of new tools and solutions to strengthen in vitro–in vivo relationships within the department., • Author, review, and contribute to scientific documentation and technical reports to support regulatory submissions (including scientific advice packages and responses to deficiency letters)., • Interact and collaborate scientifically with internal cross-functional project teams and external partners., • Maintain compliance with internal SOPs, regulatory guidelines (ICH, EMA, FDA), and GCP/GLP quality standards. What do you need? • University degree in Pharmacy, Bioinformatics, Biopharmaceutics, or other related sciences., • PhD in data modeling or related field is a plus., • Strong background in pharmacokinetics and IVIVC., • Knowledge of in vitro dissolution testing (biorelevant/biopredictive API and formulation testing)., • Hands-on experience with programming languages such as R or Python., • Experience with pharmacometric and PBPK platforms such as Phoenix, NONMEM, Simcyp, GastroPlus, PK-Sim, or equivalent tools., • High level of English (spoken and written)., • Intermediate level of Spanish. Our benefits! ⏰Flexible entry schedule from Monday to Friday (full-time, 40 hours). 📜Permanent contract 💸Attractive salary package. 🥼 Life and accident insurance. 🍽️ Company cafeteria (free). 🥼 Co-payment on voluntary health insurance. 💸Benefits & Savings Club. 📈Development plans, internal mobility policy. ⭐And many more! How will the selection process be? 🕵️ ➡️Stay alert to your phone and email! Most likely, the first thing we will do is contact you through one of these channels. ➡️Get ready! We will continue with an in-person/virtual interview depending on availability and as we agree; the process may include one or two interviews, and depending on the type of process, there may also be some sort of test. ➡️Wait for the result! We care that in each selection process you feel guided and know what to expect from us, so we will try to inform you about the status of the process at all times. 🔷Do you think this offer is not for you?🔷 Follow us on social media like LinkedIn/Instagram and stay tuned for any openings we post: the opportunity to become a new Insuder is waiting! #InsudPharma #Challenger #Insuder #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must be in harmony with the needs and demands of society, and therefore undertakes a commitment to equal opportunity and treatment between men and women, as set out in current regulations—Organic Law 3/2007—and we do not discriminate against anyone based on ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

🛰️ Indra Space – Leading the Next Generation of Space Systems 🌌 At Indra Space, we are on a mission to redefine the European space industry by delivering high‑performance small satellite solutions for LEO missions. Our ambition? To become a leading company in end‑to‑end satellite systems, driving innovation in: • Position, Navigation & Timing (PNT), • Secure Communications, • Earth Observation & ISR, • Space Domain Awareness (SDA) and Space Traffic Management (STM), • Science & space exploration As the Space Business Unit of Indra Group, we combine cutting‑edge technology with a full value‑chain approach—from satellite design and integration to ground segment and operations. With the integration of Deimos and strategic participation in Hispasat and Hisdesat, we are scaling Europe’s space autonomy and contributing to flagship programs like IRIS², Galileo, EGNOS, and Copernicus. 💡 What will you do? • Support mechanical assembly, integration and alignment of units and subsystems in satellite AIT campaigns., • Verify mechanical and thermal interfaces between equipment and structural elements., • Prepare and execute environmental test campaigns: vibration, thermal vacuum, shock, EMC., • Assist in the design, development and maintenance of Mechanical Ground Support Equipment (MGSE) and test fixtures., • Implement and document test procedures, validation reports and traceability for mechanical and thermal verification., • Collaborate with systems, electrical and test engineering teams to ensure correct mechanical configuration and test readiness., • Contribute to continuous improvement of AIT processes, tooling and documentation within the mechanical domain., • Ensure compliance with applicable space and defence standards (MIL‑STD, ECSS, IPC, ISO 9001)., • Interface with systems, design and production teams to ensure complete test coverage through qualification and delivery. 🎯 What are we looking for? • Degree in Aerospace Engineering, Industrial Engineering or equivalent., • More than 4 years of experience in relevant AIT mechanical roles., • Experience or training in mechanical and electrical integration of equipment and in executing functional and environmental tests., • Solid understanding of mechanical interfaces, structural assembly and thermal constraints during integration and testing., • Ability to work with electrical schematics, wiring diagrams, ICDs, test procedures and technical manuals., • Familiarity with controlled environments (ISO 8 / ISO 5), contamination control, ESD protection and grounding practices., • Experience in the specification, design or implementation of MGSE and/or EGSE., • English level B2 minimum., • Availability to work in a hybrid model in Madrid. Don’t worry if you don’t meet 100% of the requirements. Apply, learn about our proposal, and show us what you can bring! 🚀 What we offer • Work Your Way: Flexible hours so you can balance life and work effortlessly., • Open Culture: Direct communication and a friendly environment where your voice matters., • Innovation at Its Core: Be part of groundbreaking projects with global impact., • People First: A collaborative team that supports and celebrates your success., • Career Acceleration: Continuous feedback and annual reviews to help you grow., • Stability You Can Trust: Long‑term projects in a leading company with a future vision., • Global Reach: Your work will influence major international initiatives., • Mobility Opportunities: Explore projects across Spain and beyond., • Lifelong Learning: Access Open University programs and 3,000+ Udemy for Business courses. ✨ Your next big opportunity is here. Ready to make an impact? Apply today!

You will advise on contracts across EMEA operations, ensure legal compliance, manage risks, and collaborate with internal teams and external advisors to support our renewable energy projects. Draft, review, and negotiate agreements, providing clear legal guidance to operational and technical teams.

As Manager of Pharmaceutical Development – External Operations, you will lead, coordinate and supervise pharmaceutical development projects carried out at company 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. Specific responsibilities: • Provide strategic oversight of R&D projects developed oorganization 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; define annual objectives aligned with the company's strategy and foster a culture of innovation, involvement and continuous improvement., • 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, 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. Qualifications: • 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 semi-solid and solid oral forms (most solids); practical experience in scale-up, technology transfer and regulatory submissions (FDA/EMA and others) required., • Fluency in English (spoken/written); Spanish and/or other languages will be a significant advantage., • Proven leadership of multidisciplinary and multicultural teams; able to align diverse stakeholders in a highly dynamic and matrix environment., • Excellent project management, negotiation and interpersonal skills; proven track record in problem solving, innovation and meeting objectives on time and within budget., • Willingness to travel internationally to external sites and collaborating organisations as necessary.

🛰️ Indra Space – Leading the Next Generation of Space Systems 🌌 At Indra Space, we are on a mission to redefine the European space industry by delivering high-performance small satellite solutions for LEO missions. Our ambition? To become a leading company in end-to-end satellite systems, driving innovation in: • Position, Navigation & Timing (PNT), • Secure Communications, • Earth Observation & ISR, • Space Domain Awareness (SDA) and Space Traffic Management (STM), • Science & space exploration As the Space Business Unit of Indra Group, we combine cutting-edge technology with a full value chain approach—from satellite design and integration to ground segment and operations. With the integration of Deimos and strategic participation in Hispasat and Hisdesat, we are scaling Europe’s space autonomy and contributing to flagship programs like IRIS², Galileo, EGNOS, and Copernicus. 💡 What will you do? • Support the Assembly, Integration and Testing (AIT) activities of space systems., • Perform mechanical and electrical integration of units and subsystems., • Execute functional, RF, and environmental test campaigns (vibration, thermal vacuum, EMC, etc.)., • Implement and execute test procedures ensuring compliance with design requirements., • Verify interfaces and support the validation of the space system throughout satellite qualification., • Work with wiring diagrams, electrical schematics, ICDs, and technical manuals to guarantee consistency and traceability., • Operate within controlled environments (ISO 8 / ISO 5), following ESD, contamination control and safety procedures., • Collaborate with multidisciplinary teams within the AIT department during project execution. 🎯 What are we looking for? • Aerospace, Industrial Engineering MSc or equivalent., • 3–5 years of experience in relevant AIT or testing positions., • Experience or training in mechanical and electrical integration of equipment and subsystems, and in executing functional or environmental tests., • Ability to work with electrical schematics, wiring diagrams, test procedures, and ICDs., • Familiarity with controlled environments (ISO 8 / ISO 5), ESD, cleanliness, and grounding protocols., • Proven experience in the specification, design, or implementation of Electrical Ground Support Equipment (EGSE)., • English level B2 minimum., • Availability to work in a hybrid model in Madrid. Don’t worry if you don’t meet 100% of the requirements. Apply, learn about our proposal, and show us what you can bring! 🚀 What we offer • Work Your Way: Flexible hours so you can balance life and work effortlessly., • Open Culture: Direct communication and a friendly environment where your voice matters., • Innovation at Its Core: Be part of groundbreaking projects with global impact., • People First: A collaborative team that supports and celebrates your success., • Career Acceleration: Continuous feedback and annual reviews to help you grow., • Stability You Can Trust: Long-term projects in a leading company with a future vision., • Global Reach: Your work will influence major international initiatives., • Mobility Opportunities: Explore projects across Spain and beyond., • Lifelong Learning: Access Open University programs and 3,000+ Udemy for Business courses. ✨ Your next big opportunity is here. Ready to make an impact? Apply today!

En pocas palabras Posición: IT OT Operations Localización: Azuqueca de Henares, presencial Experiencia: 5-10 años (más experiencia será valorada) ¿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? 🔎 Como IT OT Operations, tendrás la responsabilidad global de toda la Tecnología Operacional (OT) en las plantas del grupo InsudPharma. Buscamos un profesional con visión innovadora y capacidad técnica para liderar proyectos enfocados en herramientas avanzadas de gestión industrial. Responsabilidades clave: • Contribuir al desarrollo, integración y gestión de Aveva y su ecosistema de software, incluyendo add-ons y soluciones para conectar Aveva con otras aplicaciones empresariales., • Impulsar la automatización de procesos industriales., • Implementar y mantener medidas de ciberseguridad en entornos OT., • Gestionar los activos tecnológicos industriales., • Realizar monitorización y control remoto de sistemas., • Integrar soluciones OT con IT, asegurando la conectividad y eficiencia entre plataformas., • Gestionar sensores y actuadores para una correcta recopilación y uso de datos del entorno físico, • Integrar los sistemas de control industrial (ICS), como SCADA y DCS, • Aplicar normativas de cumplimiento específicas del sector farma., • Garantizar la correcta operación en aplicaciones industriales, preferentemente en pharma. ¡El reto! 🚀 • Impulsar la evolución tecnológica de Aveva (SCADA) y desarrollar integraciones eficientes con otros sistemas como ERP, MES y soluciones específicas del sector., • Integrar la infraestructura OT a nivel global., • Realizar proyectos de automatización y digitalización en colaboración con otros departamentos., • Asegurar la adherencia a regulaciones y estándares de la industria farmacéutica., • Evaluar y reportar KPIs clave relacionados con operaciones OT. ¿Qué necesitas? • Formación: Ingeniería o profesional en Tecnología de la Información., • Experiencia: 5-10 años en OT, industrial y desarrollo/integración de Aveva (o sistemas SCADA similares; experiencia superior será considerada positivamente)., • Conocimientos específicos: Industrial Control Systems, SCADA (especialmente Aveva), DCS, sensores/actuadores, automatización, ciberseguridad, asset management, integración IT-OT, compliance farmacéutico., • Experiencia en desarrollo de add-ons/plugins y conexiones entre Aveva y otras plataformas (ERP, MES, etc.)., • Idiomas: Español e inglés fluido (otros idiomas serán valorados)., • Disponibilidad para viajes ocasionales (10% aprox.)., • Conocimiento del sector pharma o alimentación/bebidas. ¡Nuestros beneficios! ⏰Horario flexible de lunes a viernes con entrada de 08:00 a 09:30 y salida desde las 16:30 en adelante en función de la hora de entrada 📜Contrato indefinido 💸Atractivo paquete salarial según valía 🥼 Seguro de vida y accidentes 🍽️ Comedor de empresa (gratuito) 🥼 Copago en el seguro voluntario de salud 💸Club de Beneficios y Ahorro 📈Planes de desarrollo, política de movilidad interna ⭐¡Muchos más! ¿Cómo será el proceso de Selección? 🕵️ ➡️¡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. 🔷¿Crees que esta oferta no es para ti? 🔷 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.

About us: 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). We are looking for a QA TECHNICIAN for our plant, LICONSA Overview Assure compliance of GMP, regulatory and internal standards according to quality policies and applicable requirements within the organization. Actively participate in the CAPAs, CCs and complaints management, preparation of PQRs, supplier homologation and update in accordance to internal procedures, GMPs rules, Authorities and customers requirements. EU & US GMP compliance. Global Responsibility -Raw material suppliers homologation and sytem maintenance, risk assessment performance. Audits annual plan preparaton and support regarding the audit performance. The role is a contact person of the company regarding quality queries to be managed with raw material suppliers or external services. -Quality complaints from customers: register, investigation and response. Recurrence and tendency identification. -PQR preparation according to timelines included in the annual plan, internal procedures and TA in force. -CAPA and CC system: register, evaluation and follow up. Performance of the specific task assigned to. -Training: GMP basic training to new staff. Register and follow up. -SOPs: to prepare or update specific SOP related to the activitivities in charge of. -Collaborate in external audits from customers and Authorities and conduct shelf- inspections according to the annual plan. -Support to Customers and Authorities request for quality and technical issues. Competencies/Career level • Education: Degree in Pharmacy or Chemistry or Sciences., • Languages: Intermediate or high level of English required and bilingual in Spanish., • Experience (years/area): A minimum of 3 years’ experience in similar position., • Specific Knowledge: Knowledge of EU & US GMPs, quality systems (CAPAs, PQRs, audits support,suupplier managment, change controls, etc.) in pharmaceutical companies. SAP and Trackwise knowledge is valuable. 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.

INTEDYA es una compañía internacional, con presencia en 17 países, especializada en consultoría, auditoría, formación y soluciones tecnológicas en gestión de Calidad, Medioambiente, Compliance, Seguridad Alimentaria, Laboral y de la Información. En la actualidad contamos con una red mundial de más de 80 oficinas en Europa y América, y colaboramos con diversas organizaciones en busca de la excelencia empresarial y el desarrollo competitivo. INTEDYA en Expansión Global Dentro de nuestro ambicioso proyecto de expansión, INTEDYA busca incorporar perfiles emprendedores con trayectoria profesional en áreas directivas, comerciales y/o técnicas para ocupar la posición de Director/a Asociado/a. Esta posición clave involucra liderar y desarrollar un nuevo proyecto empresarial alineado con la filosofía y estrategia de la compañía. Perfil del Candidato/a Seleccionamos perfiles que combinen una mezcla de emprendimiento, experiencia directiva y conocimientos técnicos. Esencialmente, alguien que no solo tenga la visión y la capacidad para liderar, sino que también esté alineado con los valores y la filosofía de la empresa para ello se identifica el perfil ideal con: Profesionales en el punto decisivo de su carrera profesional en el que estén en disposición y capacidad de emprender su propio negocio dentro de la red empresarial de INTEDYA. Tener un conocimiento profundo del entorno económico y social de su zona de actividad. Disponer de experiencia previa en gestión de equipos y/o unidades de negocio y/o departamentos corporativos. Estar en capacidad y disposición de iniciar actividades de manera autónoma. Misión del Director/a será: Liderar un nuevo proyecto empresarial con el soporte integral de INTEDYA, incluyendo capacitación, metodología y recursos tecnológicos. Alcanzar objetivos de su negocio alineados con la estrategia global, implementando el exclusivo modelo empresarial de INTEDYA en su área geográfica. Gestionar la cuenta de resultados de su oficina, garantizando la dirección y liderazgo ético y profesional del equipo. ¿Qué Buscamos? Interés definitivo en emprender un negocio como representante franquiciado/a en el ámbito de Consultoría, Auditoría y Formación especializada. Recursos iniciales para iniciar la actividad empresarial. Personas que estén dispuestas a formarse y aprender, continuando su desarrollo profesional. Si se encuentra en un momento clave de su carrera, donde emprender representa el próximo gran desafío, y desea capitalizar sus experiencias en un proyecto ambicioso y retador, le invitamos a presentar su candidatura para dirigir una nueva oficina asociada de INTEDYA.

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