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In a nutshell Position: Pharmaceutical Development Manager - External Operations Location: Azuqueca de Henares Experience: More than 5 years in the development of the position and duties described Want to know more? 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. What are we looking for? 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. The challenge! 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. Specific responsibilities • 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; define annual objectives aligned with the company's strategy and foster a culture of innovation, engagement 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 (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. What do you need? • 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; 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 needed., • Passion for quality, patient safety, and making a difference in global health. Our benefits! ⏰Monday to Friday working hours, with flexible start times between 8:00 a.m. and 9:30 a.m. and finish times depending on start time, from 4:30 p.m. onwards. 📜Permanent contract. 💸Attractive salary package. 🥼 Life and accident insurance. 🥼 Co-payment for voluntary health insurance. 💸Benefits and Savings Club. 📈Development plans, internal mobility policy. ⭐And much more! COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must be in line with the needs and demands of society, and therefore is committed to equal opportunities and treatment between men and women, as set out in current legislation on the matter -Organic Law 3/2007, and we do not discriminate against anyone on the basis of ethnicity, religion, age, sex, nationality, marital status, emotional or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

At a glance 📌 Location: Azuqueca de Henares, Spain Work model: Hybrid Contract: Permanent Experience: Previous experience in pharmaceutical launches, project coordination, or cross-functional roles within the pharma industry Want to know more? 👇 At Xiromed, we are committed to making high-quality, affordable medicines accessible to patients across Europe. Operating in a dynamic and international environment, we work cross-functionally with internal teams and external partners to bring new products to market efficiently, reliably, and in line with the highest quality and regulatory standards. We are looking for a Launch Specialist to support the launch of Xiromed’s EU portfolio pipeline. This role will be responsible for planning, coordinating, and executing launch activities across multiple markets, ensuring that each launch is technically prepared, aligned with business goals, and delivered on time. You will play a key role in maximizing launch value and margin across our markets: Sweden, Denmark, Finland, Norway, Iceland, Germany, the Netherlands, the United Kingdom, Italy, and Poland. If you enjoy working in a fast-paced pharmaceutical environment, coordinating with multiple stakeholders, and driving product launches from planning to execution, this could be a great opportunity for you. What will you do? 🚀 • Lead new launch projects and strategic initiatives linked to new commercial opportunities., • Lead dose dispense projects across Europe and help define the best strategy for hospital and retail launches., • Coordinate cross-functional activities with Business Development, Supply, Logistics, Regulatory, Design, Commercial, IP, Pharmacovigilance, and QA/QC., • Work closely with commercial teams to ensure prioritization is up to date and business needs are clearly understood., • Help define the best launch strategy for each product, including pricing and market access considerations., • Identify risks, opportunities, and process improvement areas, while exploring new sectors and growth opportunities., • Collaborate with internal and external partners to coordinate launch activities and ensure all requirements are completed on time for product supply., • Lead portfolio optimization activities, including pack size optimization, COGs reduction, manufacturing improvements, and logistics improvements., • Maintain and regularly update the overall launch plan, reporting progress and status to relevant stakeholders., • Maintain databases in SAP, IBP, and CRM., • Ensure MMDD maintenance for serialization purposes., • Collaborate with all involved functions to ensure launches are produced according to information approved by Health Authorities., • For products with aRMMs, ensure distribution is completed effectively before launch., • Align with Logistics and QA to ensure appropriate transport conditions are in place and that required agreements and audits are completed. What are we looking for? 🤓 • Bachelor’s degree in Pharmacy, Chemistry, Biotechnology, Industrial Engineering, or a related field., • Experience in the pharmaceutical industry, ideally in product launches, project management, supply, regulatory, quality, or related cross-functional environments., • Strong understanding of launch planning and cross-functional coordination in a regulated environment., • Knowledge of GxP/GMP and pharmaceutical regulatory requirements., • Experience working with internal and external stakeholders across different markets., • Familiarity with pricing, market access, supply chain, logistics, and commercial launch strategy will be considered a strong plus., • Experience with SAP, IBP, CRM, and Excel., • Strong project management and coordination skills., • Ability to identify risks, solve problems, and manage multiple priorities at the same time., • Structured way of working, with strong attention to detail and execution., • Strong communication and stakeholder management skills., • Professional level of English, both written and spoken., • Ability to work effectively in an international and cross-functional environment. What do we offer? 👏 • 📜 Permanent contract, • ⏰ Flexible working hours, • 🌍 International exposure across multiple European markets, • 📚 Learning and development opportunities, • 🚀 A key role with high visibility and real business impact, • 💊 The opportunity to contribute to the launch of medicines that improve patients’ access to treatment What can you expect from the recruitment process? 🕵️ • Initial contact by phone or email, • First conversation with the Talent team, • 1–2 interviews with the hiring team/manager, • Ongoing communication throughout the process Not the right opportunity for you? 🔷 Follow Xiromed on LinkedIn to stay updated on future career opportunities. Equal Opportunities At Xiromed, we are committed to building an inclusive workplace where everyone is treated with respect and given equal opportunities. We welcome applications from all qualified candidates regardless of gender, gender identity or expression, age, ethnic or social background, nationality, religion, sexual orientation, disability, or any other protected characteristic.

¿Te apasiona el laboratorio microbiológico y quieres formar parte de una planta de inyectables con altos estándares de calidad? Esta es tu oportunidad. Desde la División de Hi Talent de Grupo Crit seleccionamos analistas con experiencia en el área de microbiología para incorporarse al equipo de Control de Calidad de una multinacional farmacéutica. 📍 Ubicación: Azuqueca de Henares 📄 Contrato indefinido 🧪 Área: Control de Calidad – Microbiología 🔬 ¿Cuál será tu misión? • Realizar muestreo de agua para inyectables y agua purificada, vapor puro, nitrógeno y aire comprimido., • Monitorización ambiental en salas blancas, • Ensayos microbiológicos (bioburden, identificaciones, Media Fill, etc.), • Análisis, registro y reporte de resultados, • Soporte en auditorías e inspecciones regulatorias ✅ ¿Qué buscamos? • Formación en Análisis y Control de Calidad o similar (FP o Grado Superior), • Al menos 1 año de experiencia en laboratorio farmacéutico en microbiología, • Muy valorable experiencia en entornos de inyectables ⭐ ¿Qué ofrecemos? • Contrato indefinido desde el inicio, • Turnos rotativos de lunes a viernes (3 turnos, mañana, tarde y noche), • Salario competitivo + pluses, • Seguro de vida + opción a seguro médico, • Entorno técnico, estable y con aprendizaje continuo 👉 Si buscas un entorno donde crecer en microbiología dentro de la industria farmacéutica, ¡queremos conocerte!

1、外包劳工管理：管理外包劳工供应商（包括新供应商开发、定期加成率审查与谈判、考勤管理、账单审核与支付等）。 1、Outsourcing Labor Vendor Management：Manage outsourcing labor vendors (including new vendor sourcing, periodical markup review and negotiation, time & attendance management, bill review and processing, etc.). 2、人才招聘与入职管理：监督小时工及正式员工的招聘流程，确保新员工招聘、入职和培训的及时性，以满足公司的人才需求。 2、Talent Acquisition & Onboarding：Oversee the talent acquisition process for hourly and salaried hires, ensuring that recruiting, new hire onboarding, and orientation meet the company's staffing needs in a timely manner. 3、组织目标对齐：与仓库管理团队合作，确保人力资源战略和举措与组织目标保持一致。 3、HR Strategy Alignment：Partner with the warehouse leadership team to ensure HR initiatives are aligned with organizational goals and objectives. 4、绩效管理：参与绩效目标制定、绩效评估，管理绩效改进计划，并奖励优秀员工。 4、Performance Management：Take part in objectives setting, performance discussions, managing performance improvement, and recognizing high performance. 职位描述 1、学历要求：本科及以上学历。 1、Education：Bachelor’s degree required. 2、工作经验：具备仓库劳动力管理经验优先，熟悉外包劳工供应商管理，并具备谈判能力。 Work Experience：Prior experience in warehouse labor management is preferred; candidates should be familiar with managing outsourced labor suppliers and possess strong negotiation skills. 3、人力资源相关经验，有物流行业 HR 经验者优先。 3、HR-related experience (HR experience in logistics setting is highly preferred). 4、技能要求：具备良好的人际沟通、谈判能力、团队协作能力及供应商管理技能。 4、Strong interpersonal communication, negotiation, collaboration, and vendor management skills required. 5、熟练使用办公软件（如 Word、Excel、PPT 等）和相关管理工具。 5、Proficient in office software (e.g., Word, Excel, PPT) and relevant management tools. 6、语言要求，需具备英语和普通话的语言能力，能进行有效的沟通和协调。 6、Language requirements: Applicants must be proficient in English and Mandarin Chinese, and be able to communicate and coordinate effectively.

IBERCACAO, PERTENECIENTE AL GRUPO LACASA, IMPORTANTE GRUPO DEL SECTOR GRAN CONSUMO-ALIMENTACION, SELECCIONA PARA SU PLANTA DE QUINTANAR DE LA ORDEN (TOLEDO).

At a glance 📌 Location: Azuqueca de Henares, Spain Work model: Hybrid Contract: Permanent Experience: Previous experience in pharmaceutical launches, project coordination, or cross-functional roles within the pharma industry Want to know more? 👇 At Xiromed, we are committed to making high-quality, affordable medicines accessible to patients across Europe. Operating in a dynamic and international environment, we work cross-functionally with internal teams and external partners to bring new products to market efficiently, reliably, and in line with the highest quality and regulatory standards. We are looking for a Launch Specialist to support the launch of Xiromed’s EU portfolio pipeline. This role will be responsible for planning, coordinating, and executing launch activities across multiple markets, ensuring that each launch is technically prepared, aligned with business goals, and delivered on time. You will play a key role in maximizing launch value and margin across our markets: Sweden, Denmark, Finland, Norway, Iceland, Germany, the Netherlands, the United Kingdom, Italy, and Poland. If you enjoy working in a fast-paced pharmaceutical environment, coordinating with multiple stakeholders, and driving product launches from planning to execution, this could be a great opportunity for you. What will you do? 🚀 • Lead new launch projects and strategic initiatives linked to new commercial opportunities., • Lead dose dispense projects across Europe and help define the best strategy for hospital and retail launches., • Coordinate cross-functional activities with Business Development, Supply, Logistics, Regulatory, Design, Commercial, IP, Pharmacovigilance, and QA/QC., • Work closely with commercial teams to ensure prioritization is up to date and business needs are clearly understood., • Help define the best launch strategy for each product, including pricing and market access considerations., • Identify risks, opportunities, and process improvement areas, while exploring new sectors and growth opportunities., • Collaborate with internal and external partners to coordinate launch activities and ensure all requirements are completed on time for product supply., • Lead portfolio optimization activities, including pack size optimization, COGs reduction, manufacturing improvements, and logistics improvements., • Maintain and regularly update the overall launch plan, reporting progress and status to relevant stakeholders., • Maintain databases in SAP, IBP, and CRM., • Ensure MMDD maintenance for serialization purposes., • Collaborate with all involved functions to ensure launches are produced according to information approved by Health Authorities., • For products with aRMMs, ensure distribution is completed effectively before launch., • Align with Logistics and QA to ensure appropriate transport conditions are in place and that required agreements and audits are completed. What are we looking for? 🤓 • Bachelor’s degree in Pharmacy, Chemistry, Biotechnology, Industrial Engineering, or a related field., • Experience in the pharmaceutical industry, ideally in product launches, project management, supply, regulatory, quality, or related cross-functional environments., • Strong understanding of launch planning and cross-functional coordination in a regulated environment., • Knowledge of GxP/GMP and pharmaceutical regulatory requirements., • Experience working with internal and external stakeholders across different markets., • Familiarity with pricing, market access, supply chain, logistics, and commercial launch strategy will be considered a strong plus., • Experience with SAP, IBP, CRM, and Excel., • Strong project management and coordination skills., • Ability to identify risks, solve problems, and manage multiple priorities at the same time., • Structured way of working, with strong attention to detail and execution., • Strong communication and stakeholder management skills., • Professional level of English, both written and spoken., • Ability to work effectively in an international and cross-functional environment. What do we offer? 👏 • 📜 Permanent contract, • ⏰ Flexible working hours, • 🌍 International exposure across multiple European markets, • 📚 Learning and development opportunities, • 🚀 A key role with high visibility and real business impact, • 💊 The opportunity to contribute to the launch of medicines that improve patients’ access to treatment What can you expect from the recruitment process? 🕵️ • Initial contact by phone or email, • First conversation with the Talent team, • 1–2 interviews with the hiring team/manager, • Ongoing communication throughout the process Not the right opportunity for you? 🔷 Follow Xiromed on LinkedIn to stay updated on future career opportunities. Equal Opportunities At Xiromed, we are committed to building an inclusive workplace where everyone is treated with respect and given equal opportunities. We welcome applications from all qualified candidates regardless of gender, gender identity or expression, age, ethnic or social background, nationality, religion, sexual orientation, disability, or any other protected characteristic.

INTERNATIONAL RECRUITMENT & HR EXPERTS ACROSS THE PLASTICS, PACKAGING, SPECIALITY CHEMICALS, LIFE SCIENCES, BIOPOLYMER, FOOD ADDITIVES & INGREDIENTS, ENERGY AND RECYCLING SECTORS SINCE 1975. HR Manager | Spain (Borox) | Part-Time 24–36 Hours per Week A leading international manufacturing organisation is seeking an experienced HR Manager to lead the people agenda at its Spanish production site. This is a strategically important role, acting as the key HR business partner to site leadership while connecting the Spanish operation with the wider European HR function. The successful candidate will play a central role in workforce planning, employee engagement, organisational development and operational HR performance, while ensuring corporate HR policies are effectively implemented at site level. Key Responsibilities: • Act as the primary HR partner to the Spanish site leadership team, • Support workforce planning, organisational development and people strategy, • Lead employee engagement and retention initiatives, • Ensure HR policies and procedures are implemented in line with corporate standards and Spanish legislation, • Manage the full employee lifecycle from recruitment through to termination, • Lead payroll coordination with third-party providers, • Oversee works council responsibilities and local compliance, • Create and manage annual training plans and development initiatives, • Collaborate with European HR leadership on regional projects, systems and initiatives, • Support HR process improvement and modernisation across the site Candidate Profile: We are seeking a collaborative, commercially aware and forward-thinking HR professional with experience operating in a manufacturing or industrial environment. Key requirements include: • Proven HR leadership or HR business partnering experience within manufacturing or industrial sectors, • Strong experience supporting operational leadership teams, • In-depth knowledge of Spanish labour legislation and employment frameworks, • Works council experience essential, • Experience within international or matrix organisations, • Fluent Spanish and strong English language skills, • Strong employee engagement, retention and organisational development capabilities This is an excellent opportunity for an HR professional looking to combine strategic business partnering with hands-on operational HR leadership within an international manufacturing environment. To apply please contact Jane Edwards jane.edwards@listgrove.com 0044 (0) 1789 207070 CONNECT WITH ME ON LINKEDIN. Please understand that due to the expected high number of applications, only shortlisted candidates will be contacted directly For EU roles: For reasons of better legibility, the simultaneous use of the language forms male, female and diverse (f/m/d) is avoided. All personal designations apply equally to all genders. For EU roles, candidates must be eligible to work and live in the European Union. Proof of eligibility will be required with your application Why select Listgrove? • Five Decades of Market Intelligence, • Unrivalled Industry Networks, • Recognised International brand, • HR Qualified Professionals To hear from our clients on how we have supported their search for talent and HR needs, please visit _

In a nutshell Position: Pharmaceutical Development Manager - External Operations Location: Azuqueca de Henares Experience: More than 5 years in the development of the position and duties described Want to know more? 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. What are we looking for? 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. The challenge! 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. Specific responsibilities • 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; define annual objectives aligned with the company's strategy and foster a culture of innovation, engagement 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 (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. What do you need? • 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; 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 needed., • Passion for quality, patient safety, and making a difference in global health. Our benefits! ⏰Monday to Friday working hours, with flexible start times between 8:00 a.m. and 9:30 a.m. and finish times depending on start time, from 4:30 p.m. onwards. 📜Permanent contract. 💸Attractive salary package. 🥼 Life and accident insurance. 🥼 Co-payment for voluntary health insurance. 💸Benefits and Savings Club. 📈Development plans, internal mobility policy. ⭐And much more! COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must be in line with the needs and demands of society, and therefore is committed to equal opportunities and treatment between men and women, as set out in current legislation on the matter -Organic Law 3/2007, and we do not discriminate against anyone on the basis of ethnicity, religion, age, sex, nationality, marital status, emotional or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

At a glance 📌 Location: Azuqueca de Henares, Spain Work model: Hybrid Contract: Permanent Experience: Previous experience in pharmaceutical launches, project coordination, or cross-functional roles within the pharma industry Want to know more? 👇 At Xiromed, we are committed to making high-quality, affordable medicines accessible to patients across Europe. Operating in a dynamic and international environment, we work cross-functionally with internal teams and external partners to bring new products to market efficiently, reliably, and in line with the highest quality and regulatory standards. We are looking for a Launch Specialist to support the launch of Xiromed’s EU portfolio pipeline. This role will be responsible for planning, coordinating, and executing launch activities across multiple markets, ensuring that each launch is technically prepared, aligned with business goals, and delivered on time. You will play a key role in maximizing launch value and margin across our markets: Sweden, Denmark, Finland, Norway, Iceland, Germany, the Netherlands, the United Kingdom, Italy, and Poland. If you enjoy working in a fast-paced pharmaceutical environment, coordinating with multiple stakeholders, and driving product launches from planning to execution, this could be a great opportunity for you. What will you do? 🚀 • Lead new launch projects and strategic initiatives linked to new commercial opportunities., • Lead dose dispense projects across Europe and help define the best strategy for hospital and retail launches., • Coordinate cross-functional activities with Business Development, Supply, Logistics, Regulatory, Design, Commercial, IP, Pharmacovigilance, and QA/QC., • Work closely with commercial teams to ensure prioritization is up to date and business needs are clearly understood., • Help define the best launch strategy for each product, including pricing and market access considerations., • Identify risks, opportunities, and process improvement areas, while exploring new sectors and growth opportunities., • Collaborate with internal and external partners to coordinate launch activities and ensure all requirements are completed on time for product supply., • Lead portfolio optimization activities, including pack size optimization, COGs reduction, manufacturing improvements, and logistics improvements., • Maintain and regularly update the overall launch plan, reporting progress and status to relevant stakeholders., • Maintain databases in SAP, IBP, and CRM., • Ensure MMDD maintenance for serialization purposes., • Collaborate with all involved functions to ensure launches are produced according to information approved by Health Authorities., • For products with aRMMs, ensure distribution is completed effectively before launch., • Align with Logistics and QA to ensure appropriate transport conditions are in place and that required agreements and audits are completed. What are we looking for? 🤓 • Bachelor’s degree in Pharmacy, Chemistry, Biotechnology, Industrial Engineering, or a related field., • Experience in the pharmaceutical industry, ideally in product launches, project management, supply, regulatory, quality, or related cross-functional environments., • Strong understanding of launch planning and cross-functional coordination in a regulated environment., • Knowledge of GxP/GMP and pharmaceutical regulatory requirements., • Experience working with internal and external stakeholders across different markets., • Familiarity with pricing, market access, supply chain, logistics, and commercial launch strategy will be considered a strong plus., • Experience with SAP, IBP, CRM, and Excel., • Strong project management and coordination skills., • Ability to identify risks, solve problems, and manage multiple priorities at the same time., • Structured way of working, with strong attention to detail and execution., • Strong communication and stakeholder management skills., • Professional level of English, both written and spoken., • Ability to work effectively in an international and cross-functional environment. What do we offer? 👏 • 📜 Permanent contract, • ⏰ Flexible working hours, • 🌍 International exposure across multiple European markets, • 📚 Learning and development opportunities, • 🚀 A key role with high visibility and real business impact, • 💊 The opportunity to contribute to the launch of medicines that improve patients’ access to treatment What can you expect from the recruitment process? 🕵️ • Initial contact by phone or email, • First conversation with the Talent team, • 1–2 interviews with the hiring team/manager, • Ongoing communication throughout the process Not the right opportunity for you? 🔷 Follow Xiromed on LinkedIn to stay updated on future career opportunities. Equal Opportunities At Xiromed, we are committed to building an inclusive workplace where everyone is treated with respect and given equal opportunities. We welcome applications from all qualified candidates regardless of gender, gender identity or expression, age, ethnic or social background, nationality, religion, sexual orientation, disability, or any other protected characteristic.

¿Te apasiona el laboratorio microbiológico y quieres formar parte de una planta de inyectables con altos estándares de calidad? Esta es tu oportunidad. Desde la División de Hi Talent de Grupo Crit seleccionamos analistas con experiencia en el área de microbiología para incorporarse al equipo de Control de Calidad de una multinacional farmacéutica. 📍 Ubicación: Azuqueca de Henares 📄 Contrato indefinido 🧪 Área: Control de Calidad – Microbiología 🔬 ¿Cuál será tu misión? • Realizar muestreo de agua para inyectables y agua purificada, vapor puro, nitrógeno y aire comprimido., • Monitorización ambiental en salas blancas, • Ensayos microbiológicos (bioburden, identificaciones, Media Fill, etc.), • Análisis, registro y reporte de resultados, • Soporte en auditorías e inspecciones regulatorias ✅ ¿Qué buscamos? • Formación en Análisis y Control de Calidad o similar (FP o Grado Superior), • Al menos 1 año de experiencia en laboratorio farmacéutico en microbiología, • Muy valorable experiencia en entornos de inyectables ⭐ ¿Qué ofrecemos? • Contrato indefinido desde el inicio, • Turnos rotativos de lunes a viernes (3 turnos, mañana, tarde y noche), • Salario competitivo + pluses, • Seguro de vida + opción a seguro médico, • Entorno técnico, estable y con aprendizaje continuo 👉 Si buscas un entorno donde crecer en microbiología dentro de la industria farmacéutica, ¡queremos conocerte!

Desde la División de Hi Talent de Grupo Crit seleccionamos analistas con experiencia en el área de microbiología para incorporarse al equipo de Control de Calidad de una multinacional farmacéutica. Te apasiona el laboratorio microbiológico y quieres formar parte de una planta de inyectables con

Te apasiona el laboratorio microbiológico y quieres formar parte de una planta de inyectables con altos estándares de calidad? Esta es tu oportunidad.Desde la División de Hi Talent de Grupo Crit seleccionamos analistas con experiencia en el área de microbiología para incorporarse al equipo de C

Te apasiona el laboratorio microbiológico y quieres formar parte de una planta de inyectables con altos estándares de calidad? Esta es tu oportunidad. Desde la División de Hi Talent de Grupo Crit seleccionamos analistas con experiencia en el área de microbiología para incorporarse al equipo de

Actual Talent is the talent acquisition consultancy that offers Specialised Search, RPO and Talent Solutions. We do this through talent acquisition and development solutions that focus on people, diversity and inclusion, innovation, and cutting-edge technology.

Actualmente se busca un/a "Gerocultor/a" para incorporar a la residencia de SENIORS ubicada en Guadalajara, en la localidad de Cabanillas del Campo. Estamos buscando un/a "Gerocultor/a" para incorpora a la red de residencias de personas mayores SENIORS, una organización dentro del Grupo Clariane.

Te apasiona la hospitalidad y el servicio al cliente? Estamos buscando un/a Recepcionista para un nuestros hotel en Toledo. Descuentos en servicios y alojamiento del hotel. Manejar el sistema de gestión hotelera (PMS) y realizar cobros o cierres de caja cuando sea necesario.

Gestiona estrategias de desarrollo, retención y adquisición de talento, alineando la estrategia con los objetivos del negocio.

La persona seleccionada se responsabilizará del ciclo contable completo y dará soporte en la elaboración y presentación de las principales obligaciones fiscales Funciones - Gestión del ciclo contable completo de una cartera de clientes - Registro y contabilización de facturas, movimientos ba