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Role: QA EBR Technician Location: León Experience: 1–3 years. Want to find out more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialist knowledge and expertise 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, adding value to human and animal health. INSUD PHARMA’s activities are organised into three synergistic business areas: Industrial (Chemo), Branded (Exeltis) and Biotechnology (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialised R&D centres, 12 sales offices and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Global Responsibility Comply with the GMP standards for medicinal and combination products for human use. Review, control and ensure compliance of Electronic Batch Records (EBR) and related manufacturing documentation in accordance with internal procedures, GMP rules and Authority and customers requirements, ensuring data integrity, traceability, accuracy and completeness of batch documentation prior to batch disposition and/or release activities. Specific Responsibilities · Develop standard operating procedures (general quality and departmental) related to batch record review, good documentation practices and electronic batch record management to ensure that all steps are properly defined and comply with internal and external regulations applicable in each case. · Review and approve internal SOPs related to EBR management, documentation review and GMP documentation practices. · Review Electronic Batch Records and associated manufacturing documentation to ensure completeness, accuracy, consistency and compliance with approved procedures and manufacturing instructions. · Verify that all critical process steps, controls, calculations, material reconciliations and manufacturing data are correctly documented in the EBR system and related records. · Ensure that all entries, corrections, comments and changes in the electronic records are properly documented and compliant with data integrity and GMP requirements. · Manage discrepancies identified during batch record review and coordinate with Production and other involved departments their investigation, correction and closure in accordance with internal procedures. · Support root cause analysis and trend analysis related to documentation errors, batch record discrepancies and recurring issues detected during EBR review. · Coordinate with Production, Engineering, Maintenance, Validation and other departments to ensure that any issue impacting batch documentation is properly assessed and resolved. · Review and verify that deviations, change controls or other quality events impacting the batch are properly linked, assessed and documented in the batch record package when applicable. · Ensure the proper management, traceability and archive of GMP documentation related to batch manufacturing records. · Support the implementation, maintenance and continuous improvement of electronic batch record systems and associated documentation workflows. · Participate in training activities related to Good Documentation Practices, GMP requirements and proper use/completion of Electronic Batch Records. · Support external audits and inspections according to the Annual Plan to assess compliance of batch documentation practices, data integrity requirements and the GMP system. · Participate in internal audits related to documentation practices, EBR processes and manufacturing records. · Support the Qualified Person and batch release activities through timely and accurate review of manufacturing documentation. · Support on quality investigations, batch documentation assessments and product quality issues related to manufacturing records. · Support to quality activities according to the appropriate training. Competencies/Career level Innovation, customer oriented, communication, team work, adaptability/flexibility, productivity, self-development, sense of urgency, initiative. Attention to detail, analytical mindset, compliance mindset, documentation rigor and organizational skills are especially valuable for this position. Requirements and personal skills · Education: Degree in Pharmacy or Chemistry or Sciences. · Languages: Intermediate or high level of English and bilingual in Spanish. · Experience (years/area): A minimum of 3 years' experience in similar position for a senior position. Experience in GMP documentation review, manufacturing records, batch record review or pharmaceutical production quality activities is highly valuable. · Specific Knowledge: Knowledge of GMP documentation systems, good documentation practices, batch record review processes, deviations/non-conformities, data integrity principles and quality systems in production plants. Experience with Electronic Batch Records (EBR) systems will be highly valued. · Travels: Not required. · Personal skills: Good communication skills, proactivity, good working under pressure, team working, problem-solving, good organizational skills, persistence and high attention to detail. COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma Group recognises that business management must be aligned with the needs and demands of society, and therefore is committed to equal opportunities and equal treatment for men and women, as set out in the relevant legislation in force – Organic Law 3/2007 – and we do not discriminate against anyone on the grounds of ethnicity, religion, age, sex, nationality, marital status, emotional or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

Position: QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight Location: León (on-site) Experience: At least 3 years’ experience in similar roles within the Quality department in pharmaceutical industrial settings Want to find out more? 👇 LEONFARMA is part of INSUD PHARMA, a global leader in the pharmaceutical value chain and a benchmark in the research, development, manufacture and marketing of pharmaceutical products that contribute to human and animal health. Our purpose is to transform the industry through innovation, excellence and a commitment to sustainable development. Ready to be a #Challenger at LEONFARMA? 💪 What are we looking for? 🔎 We are looking for a QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight who is passionate about the industrialisation of new products. General Responsibility Ensure quality oversight of production-related activities in a GMP-regulated manufacturing environment, acting as a key quality partner for operations on the shop floor. The role is responsible for leading and coordinating investigations, change controls and CAPAs, ensuring appropriate risk assessment, impact evaluation and timely closure in compliance with quality and regulatory requirements. In addition, the position provides real-time QA support to production, reinforcing GMP compliance, issue resolution and continuous improvement across daily manufacturing operations. Specific Responsibilities • Lead and manage quality investigations related to deviations associated with production activities., • Perform and support root cause analysis, ensuring robust identification of underlying causes and appropriate documentation of findings., • Evaluate the impact of deviations on product quality, manufacturing processes and GMP/regulatory compliance., • Coordinate cross-functional investigation activities with Production, Engineering, Quality Control, Maintenance and other relevant departments., • Review, assess and approve change requests/change controls, ensuring proper justification, impact assessment and implementation in line with GMP requirements., • Ensure that change controls are adequately evaluated, approved, implemented and closed within established timelines., • Review and approve CAPA plans derived from investigations, audits and inspections, ensuring actions are appropriate and sustainable., • Monitor CAPA implementation and verify effectiveness prior to closure., • Provide routine QA floor oversight through regular presence in production areas, supporting real-time decision-making and compliance with approved procedures., • Support production teams during critical operations, helping resolve GMP issues promptly and reinforcing quality culture on the shop floor. Experience (area) Quality Assurance in GMP-regulated pharmaceutical or biotechnology manufacturing environments, with strong exposure to production-related quality activities. Personal skills • Adaptability to change and flexibility, • Speed without compromising on quality, • Leadership and teamwork, • Effective communication, • Compliance, integrity and sustainability, • Growth mindset, • Business focus Our benefits! 👏 📜 Permanent contract 🎯 Career progression and development within a growing international group 🏆 Ongoing training and an innovative working environment 🍏 Subsidised canteen and other employee benefits What will the recruitment process be like? 🕵️ Initial contact by phone or email with our Talent Acquisition team. 1 or 2 face-to-face interviews at our premises in León. Regular updates on the progress of the process. 🔷Do you think this role isn’t for you? 🔷 Follow us on LinkedIn and Instagram so you don’t miss out on future career opportunities! #Leonfarma #Challenger #InsudPharma #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES AT LEONFARMA, we believe in and act to promote genuine equality of opportunity. We do not discriminate on the basis of gender, ethnicity, religion, sexual orientation, disability or any other characteristic. We value diversity and talent. We’d love to meet you!

Position: QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight Location: León (on-site) Experience: At least 3 years’ experience in similar roles within the Quality department in pharmaceutical industrial settings Want to find out more? LEONFARMA is part of INSUD PHARMA, a global leader in the pharmaceutical value chain and a benchmark in the research, development, manufacture and marketing of pharmaceutical products that contribute to human and animal health. Our purpose is to transform the industry through innovation, excellence and a commitment to sustainable development. Ready to be a #Challenger at LEONFARMA? What are we looking for? We are looking for a QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight who is passionate about the industrialisation of new products. General Responsibility Ensure quality oversight of production-related activities in a GMP-regulated manufacturing environment, acting as a key quality partner for operations on the shop floor. The role is responsible for leading and coordinating investigations, change controls and CAPAs, ensuring appropriate risk assessment, impact evaluation and timely closure in compliance with quality and regulatory requirements. In addition, the position provides real-time QA support to production, reinforcing GMP compliance, issue resolution and continuous improvement across daily manufacturing operations. Specific Responsibilities • Lead and manage quality investigations related to deviations associated with production activities. • Perform and support root cause analysis, ensuring robust identification of underlying causes and appropriate documentation of findings. • Evaluate the impact of deviations on product quality, manufacturing processes and GMP/regulatory compliance. • Coordinate cross-functional investigation activities with Production, Engineering, Quality Control, Maintenance and other relevant departments. • Review, assess and approve change requests/change controls, ensuring proper justification, impact assessment and implementation in line with GMP requirements. • Ensure that change controls are adequately evaluated, approved, implemented and closed within established timelines. • Review and approve CAPA plans derived from investigations, audits and inspections, ensuring actions are appropriate and sustainable. • Monitor CAPA implementation and verify effectiveness prior to closure. • Provide routine QA floor oversight through regular presence in production areas, supporting real-time decision-making and compliance with approved procedures. • Support production teams during critical operations, helping resolve GMP issues promptly and reinforcing quality culture on the shop floor. Experience (area) Quality Assurance in GMP-regulated pharmaceutical or biotechnology manufacturing environments, with strong exposure to production-related quality activities. Personal skills • Adaptability to change and flexibility • Speed without compromising on quality • Leadership and teamwork • Effective communication • Compliance, integrity and sustainability • Growth mindset • Business focus Our benefits! Permanent contract Career progression and development within a growing international group Ongoing training and an innovative working environment Subsidised canteen and other employee benefits What will the recruitment process be like? ️ Initial contact by phone or email with our Talent Acquisition team. 1 or 2 face-to-face interviews at our premises in León. Regular updates on the progress of the process. Do you think this role isn’t for you? Follow us on LinkedIn and Instagram so you don’t miss out on future career opportunities! #Leonfarma #Challenger #InsudPharma #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES AT LEONFARMA, we believe in and act to promote genuine equality of opportunity. We do not discriminate on the basis of gender, ethnicity, religion, sexual orientation, disability or any other characteristic. We value diversity and talent. We’d love to meet you!

🚀 Profesionales del sector seguros de Salud - Proyecto Comercial.¿Tienes experiencia en seguros de salud y quieres crecer profesionalmente? Buscamos talento comercial, tanto para desarrollar tu propia cartera como para liderar y hacer crecer equipos.🎯 A quién buscamosProfesionales con experiencia en el sector asegurador o comercial, orientados a resultados, con ganas de crecer y, si lo desean, liderar un proyecto propio.✅ Qué ofrecemosAltos incentivos sin límiteFlexibilidad y autonomía realFormación continua y certificaciones oficialesSoporte de marketing y herramientas digitalesCrecimiento profesional y estructuralPosibilidad de ofrecer soluciones complementarias: ahorro, inversión, protección y productos de partners top (Sanitas NN, ING, Abanca, Caser, Mutua Madrileña, NN Employee Benefits)

Role: QA EBR Technician Location: León Experience: 1–3 years. Puede obtener más detalles sobre la naturaleza de esta vacante y lo que se espera de los solicitantes leyendo la información a continuación. Want to find out more? INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialist knowledge and expertise 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, adding value to human and animal health. INSUD PHARMA’s activities are organised into three synergistic business areas: Industrial (Chemo), Branded (Exeltis) and Biotechnology (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialised R&D centres, 12 sales offices and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Global Responsibility Comply with the GMP standards for medicinal and combination products for human use. Review, control and ensure compliance of Electronic Batch Records (EBR) and related manufacturing documentation in accordance with internal procedures, GMP rules and Authority and customers requirements, ensuring data integrity, traceability, accuracy and completeness of batch documentation prior to batch disposition and/or release activities. Specific Responsibilities · Develop standard operating procedures (general quality and departmental) related to batch record review, good documentation practices and electronic batch record management to ensure that all steps are properly defined and comply with internal and external regulations applicable in each case. · Review and approve internal SOPs related to EBR management, documentation review and GMP documentation practices. · Review Electronic Batch Records and associated manufacturing documentation to ensure completeness, accuracy, consistency and compliance with approved procedures and manufacturing instructions. · Verify that all critical process steps, controls, calculations, material reconciliations and manufacturing data are correctly documented in the EBR system and related records. · Ensure that all entries, corrections, comments and changes in the electronic records are properly documented and compliant with data integrity and GMP requirements. · Manage discrepancies identified during batch record review and coordinate with Production and other involved departments their investigation, correction and closure in accordance with internal procedures. · Support root cause analysis and trend analysis related to documentation errors, batch record discrepancies and recurring issues detected during EBR review. · Coordinate with Production, Engineering, Maintenance, Validation and other departments to ensure that any issue impacting batch documentation is properly assessed and resolved. · Review and verify that deviations, change controls or other quality events impacting the batch are properly linked, assessed and documented in the batch record package when applicable. · Ensure the proper management, traceability and archive of GMP documentation related to batch manufacturing records. · Support the implementation, maintenance and continuous improvement of electronic batch record systems and associated documentation workflows. · Participate in training activities related to Good Documentation Practices, GMP requirements and proper use/completion of Electronic Batch Records. · Support external audits and inspections according to the Annual Plan to assess compliance of batch documentation practices, data integrity requirements and the GMP system. · Participate in internal audits related to documentation practices, EBR processes and manufacturing records. · Support the Qualified Person and batch release activities through timely and accurate review of manufacturing documentation. · Support on quality investigations, batch documentation assessments and product quality issues related to manufacturing records. · Support to quality activities according to the appropriate training. Competencies/Career level Innovation, customer oriented, communication, team work, adaptability/flexibility, productivity, self-development, sense of urgency, initiative. Attention to detail, analytical mindset, compliance mindset, documentation rigor and organizational skills are especially valuable for this position. Requirements and personal skills · Education: Degree in Pharmacy or Chemistry or Sciences. · Languages: Intermediate or high level of English and bilingual in Spanish. · Experience (years/area): A minimum of 3 years' experience in similar position for a senior position. Experience in GMP documentation review, manufacturing records, batch record review or pharmaceutical production quality activities is highly valuable. · Specific Knowledge: Knowledge of GMP documentation systems, good documentation practices, batch record review processes, deviations/non-conformities, data integrity principles and quality systems in production plants. Experience with Electronic Batch Records (EBR) systems will be highly valued. · Travels: Not required. · Personal skills: Good communication skills, proactivity, good working under pressure, team working, problem-solving, good organizational skills, persistence and high attention to detail. xcskxlj COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma Group recognises that business management must be aligned with the needs and demands of society, and therefore is committed to equal opportunities and equal treatment for men and women, as set out in the relevant legislation in force – Organic Law 3/2007 – and we do not discriminate against anyone on the grounds of ethnicity, religion, age, sex, nationality, marital status, emotional or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

Profesionales del sector seguros de Salud - Proyecto Comercial. Todas las habilidades, cualificaciones y experiencia relevantes que necesitará un candidato seleccionado se enumeran en la siguiente descripción. ¿Tienes experiencia en seguros de salud y quieres crecer profesionalmente? Buscamos talento comercial , tanto para desarrollar tu propia cartera como para liderar y hacer crecer equipos . A quién buscamos Profesionales con experiencia en el sector asegurador o comercial, orientados a resultados, con ganas de crecer y, si lo desean, liderar un proyecto propio. Qué ofrecemos Altos incentivos sin límite Flexibilidad y autonomía real Formación continua y certificaciones oficiales Soporte de marketing y herramientas digitales xiphteb Crecimiento profesional y estructural Posibilidad de ofrecer soluciones complementarias: ahorro, inversión, protección y productos de partners top (Sanitas NN, ING, Abanca, Caser, Mutua Madrileña, NN Employee Benefits)

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