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

In a nutshell Aunque la experiencia profesional y las cualificaciones son clave para este puesto, asegúrese de comprobar si posee las habilidades interpersonales preferibles antes de solicitar, si se requieren. 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! xiphteb 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.

Position: Clinical Research Associate ¿Es este el siguiente paso en su carrera? Descubra si es el candidato adecuado leyendo la descripción completa a continuación. 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 Willingness to travel ~10% Languages Fluent English required Spanish (communicative level) is a plus; other languages are an asset Skills 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! xiphteb #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: Oligonucleotide Analytical Chemistry Senior ScientistINSUD 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. Habilidades, experiencia, cualificaciones... Si tiene el perfil adecuado para esta oportunidad, asegúrese de inscribirse hoy mismo. 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. We are recruiting a Oligonucleotide Analytical Chemistry Senior Scientist to join the R&D team at one of our plants located in Azuqueca de Henares. Scientist, Oligonucleotide Analytical Chemistry, you and your team will play an important role in the analysis and quality control of oligonucleotide therapeutics pipeline. Develop and deploy robust analytical methods to support in-house oligonucleotide synthesis, including novel chemistries and conjugates.Help design and manage key data pipelines.Collaborate internally and externally, representing Oligonucleotide Analytical Chemistry on project.Support analytical investigations, including root cause analysis, in collaboration with cross-functional teamsParticipate in hiring, mentoring and training of junior team members, ensuring knowledge transfer and capability development A MS degree with at least 8 years of relevant experience in analytical chemistry or a related discipline (or equivalent).Six or more years of experience using high-resolution LC/MS(-MS) methodology in a biotechnology, pharmaceutical, or academic setting.At least three years of experience utilizing modern mass spectrometry data analysis techniques, particularly as applied to biopolymers such as oligonucleotides, proteins, and/or glycans. A PhD in analytical chemistry or a related discipline with three or more years of experience.Experience with high-throughput LC/MS(-MS) data acquisition and analysis.Experience with the LC/MS(-MS) analysis of small molecules and/or biologics/oligos.Familiarity working in cross-functional matrix project team Monday to Friday working hours, with flexible start times between 8:00 a.m. Permanent contract.#Co-payment for voluntary health insurance. xcskxlj #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.

OHLA es un grupo global de infraestructuras con más de 110 años de trayectoria en constante evolución.Somos expertos en proyectos de Ingeniería Civil, singular, energías renovables, infraestructuras de transporte y servicio a las personas.Las miles de personas que integran la compañía son el

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As a Global Quality & Training Manager, you are responsible for designing, building, running, and optimizing a quality management and training unit as an integral part of CHG Global Operations, growing our specialists worldwide for the best results, efficient handling of processes, and driving quali

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Diseñar e implementar quality gates automatizados integrados en pipelines CI/CD.

As an AI Quality Analyst, you will evaluate a new personalization feature for Gemini. You will then use your analytical skills to assess the quality of the model's personalized responses, evaluating dimensions like Grounding, Integration, and Helpfulness. Exceptional Analytical Thinking: Demonstrate

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We’re Hiring: Quality Assurance (QA) Specialist.

Assessing Integration quality to ensure personal data is woven naturally into the response without robotic overnarrating. Experience in data annotation, AI quality evaluation, content moderation, or a related role is strongly preferred. As an AI Quality Analyst, you will evaluate a new personali

As an Operations Trainer & Quality Analyst, you play a critical role in improving agent performance and customer experience by connecting training, quality assurance, and operational insights. Conduct calibration sessions with stakeholders to ensure consistency in the application of quality standard

As a Global Quality & Training Manager, you are responsible for designing, building, running, and optimizing a quality management and training unit as an integral part of CHG Global Operations, growing our specialists worldwide for the best results, efficient handling of processes, and driving quali

As an Operations Trainer & Quality Analyst, you play a critical role in improving agent performance and customer experience by connecting training, quality assurance, and operational insights. Conduct calibration sessions with stakeholders to ensure consistency in the application of quality standard

Importante empresa especializada en fabricación de aparatos médicos se encuentra en búsqueda de un Quality Manager para la parte de Medical Devices.

As a Global Quality & Training Manager, you are responsible for designing, building, running, and optimizing a quality management and training unit as an integral part of CHG Global Operations, growing our specialists worldwide for the best results, efficient handling of processes, and driving quali

Importante empresa especializada en fabricación de aparatos médicos se encuentra en búsqueda de un Quality Manager para la parte de Medical Devices.

To this aim, you will design and develop ways of analyzing and visualizing relevant aspects of our datasets, with the final objective of ensuring their quality. As a Quality Analyst, you will be working in a very dynamic environment, which means that you must have a strong problem-solving ability, o

This role is xcskxlj ideal for someone who has had some exposure to quality assurance, has a strong attention to detail and a collaborative approach to maintaining high quality standards. My client are a pharmaceutical manufacturer seeking a QA Technician to support quality assurance activities with

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Edition and maintenance of Quality Agreements. SOPs and controlled documents related to Quality & R&D. Quality Assurance – Pharmaceutical Development.

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L'INTERNATIONAL QUALITY & IMPROVEMENT ENGINEER est chargé de :.

To supervise and coordinate Quality Assurance activities within assigned processes, ensuring full compliance with. Hlx are partnered with a fast-growing biologics CDMO who are growing their quality capabilities.