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Our client is a technology-driven organization that develops and distributes high-performance solutions for automotive, industrial and manufacturing environments. Operating globally, the company applies advanced materials science, surface-engineering technologies and automation to deliver precise, efficient and scalable products. Its culture is defined by operational agility, technical rigor and continuous improvement across its international supply-chain network. Mission The Purchase Specialist plays a critical role in ensuring material availability and supporting the stability of the company’s global supply chain. This position is responsible for executing tactical and strategic purchasing activities, maintaining reliable supplier performance, and securing competitive procurement conditions. The role contributes directly to operational efficiency by applying data-driven decision-making, collaborating with cross-functional teams, and supporting the adoption of digital procurement tools and automated workflows. Responsibilities Demand Planning Support and Forecast Alignment • Translate business signals, consumption patterns and production requirements into accurate purchasing needs., • Contribute to forecasting processes by coordinating with planning, production and logistics teams., • Maintain visibility of requirements through analytical platforms, dashboards and KPIs that enable timely decision-making. Strategic and Tactical Buying • Execute purchasing activities for raw materials, consumables, surface-treatment products and equipment in line with cost, quality and service objectives., • Support the development of sourcing strategies by providing market insights, supplier data and cost analyses., • Conduct negotiations on pricing, delivery terms, technical specifications and service levels to ensure sustainable value., • Maintain professional relationships with suppliers, ensuring alignment with quality, delivery reliability and continuous-improvement expectations. Operational Execution and Inventory Coordination • Manage purchase orders, confirmations, delivery schedules and updates within the ERP system., • Coordinate closely with production, warehouse and logistics teams to align purchasing actions with inventory targets and operational needs., • Monitor supplier performance, delivery accuracy and lead times, triggering corrective actions when required. Process Optimization, Digital Tools and Risk Mitigation • Support digital transformation initiatives in procurement, including ERP enhancements, automation tools and data-driven workflows., • Promote data accuracy and effective system utilization to improve decision speed and transparency., • Contribute to risk-mitigation activities such as supplier diversification, dual sourcing and compliance with internal governance and regulatory requirements. Required Qualifications • Minimum 3–5 years of experience in purchasing, procurement or supply planning within industrial, manufacturing or automotive environments., • Proven capability in commercial and technical negotiation., • Strong analytical foundation applied to demand translation, cost evaluation and inventory coordination., • Proficiency with ERP systems and purchasing platforms (e.g., SAP, Oracle, SRM tools)., • Solid understanding of supply-chain principles, supplier performance management and international logistics., • Experience collaborating with engineering, production, IT/digital and logistics teams. Preferred Experience • Exposure to digital procurement tools, automation solutions or advanced analytics., • Experience working with suppliers in materials science, manufacturing processes or engineered components., • Familiarity with continuous-improvement methodologies or quality-management frameworks.

Responsibilities: • Carry out process audits and approval of new suppliers for their incorporation into the group's panel., • Pilot the technical support to supplier with the technical departments of the group., • Carry out the homologation of the purchase components., • Pilot the action plan of the deviations detected in the homologation phase of the purchase components., • Define and maintain KPI's for monitoring the position., • Define the reception control plan for the purchase components., • Take active roles in the work of internal-external issues, risk& opportunity studies, D/FMEA studies etc., • Inform and educate to suppliers about all the requests and expectations which are introduced in hand manuals, agreements, instructions and so on. Follow-up suppliers' project documentations and take these documents convenient format and timely • Track the serial projects and supplier’s parts failure trends, take necessary actions to reduce these failure quantities and rates, • Manage suppliers’ 8D processes which are escalated, get suitable respond in each step of 8D and on time. Minimum Required Knowledge and Skills: • High School Degree • Using ability MS Office Programs, • Have at least 3 years experiences in quality departments, 1 year of experience as a SQE within productive companies, • Knowledge of ISO 9001 is required. ISO 14001 and ISO 22163 etc. systems are positively valued., • Knowledge of any of these production processes, plastic injection, aluminum casting, stamping, welding, gluing, fabric manufacturing processes, painting, machining, foaming, upholstering, cutting and sewing, press, folding, laser cutting, is valued positively., • Knowledge of Core Tools (APQP-PPAP, SPC, MSA, PFMEA, 8D), • Auditing knowledge is required, • Knowledge of: English, Spanish. We offer: • position, • for professional growth, • Salary aligned with the candidate's value, • Flexible working hours, • 30% home office

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. The Senior SW Development Engineer, develop a role as as either full-stack or front-end or back-end , being involved in all stages and all areas of software development, including Test as well as architecture design, code review, and internal tool management. The programming language required for this project is Standard C++ They are responsible for developing and implementing front-end and/or back-end software applications, including back-end design, testing, and systems integration. Key Accountabilities • Performs software engineering activities including software requirements, architecture, design, implementation and test independently., • Lead software development activities within projects at technical or at project level., • Developing SW following company procedures. Able to complete somewhat ambiguous problems and defect fixing with its corresponding test., • Works across the-full stack, or focused in back-end or front-end, building scalable solutions that drive positive user experiences and measurable business impact, • Develops new software features and infrastructure elements in support of priority business and solution requirements., • Ensures application performance, uptime, risk mitigation, scalability, and high code/application quality, • Uses agile engineering practices and various software development technologies to rapidly develop creative and efficient solutions that enhance the organization’s technology stack, • Collaborates with other squad members to implement user stories, write tests, and continuously deliver new/improved product functionality., • Will design and build software that is simple and scalable. Will write maintainable code., • Will be able to Able to review and give feedback for technical and architecture documentation., • Will know your project in a low complexity level, enough to cover your work autonomously and the environment where it works with some detail., • Will work in a project with low or medium complexity, • Will able to work autonomoslly, however you know when you have to consult the experts on the issues that appear on the projects Education: Engineer, computer Science or other Technical degree, or equivalent work experience Experience: • Approximately 5-7 years of related experience, • Experience in Software Medical Devices development that follows ISO 13485 is a plus, • Proficient in all the languages and frameworks used in the project, • Proficient in Database Queries and Database Design Skills & Capabilities: The ideal candidate for this position will exhibit the following skills and competencies: • Understand the impact of a feature. You break this down into associated tasks. You deliver frequently and predictably., • Understand your dependencies and their limitations., • Highly organized and detail-oriented, with the ability to multi-task., • Proactivity, but still work well in a team oriented environment., • Strong communication skills with the ability to communicate complex technical concepts and align the organization on decisions., • Flexibility and adaptability to a fast changing environment, • Sound problem-solving skills with the ability to quickly process complex information and present it clearly and simply, • Utilizes team collaboration to create innovative solutions efficiently, • A meaningful project that will impact the quality of laboratory software medicine worldwide, • 3 days a week working from home, • Multicultural and friendly team, • Exciting opportunities for professional development., • Ongoing training, • Social benefits: Canteen, nursery check, continius training, Doctor at the office, retirement plan..., • All the benefits according to the chemical agreement Werfen appreciates and values diversity. We are an Equal Opportunity/Affirmative Action Employer M/F/D/V. Our Purpose: We contribute to the advancement of patient care around the world through innovative specialized diagnostics JOIN US!

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. This position is part of the Product Cybersecurity Department, an organizational unit within the company that focuses on ensuring the security of its products and services. This department is responsible for implementing, managing, and overseeing cybersecurity measures specific to the development, deployment, and ongoing support of the company's products The primary responsibility of the position involves designing, implementing, testing, and managing security measures to protect computer systems, networks, and data. The role requires a deep understanding of current and emerging cybersecurity threats, as well as the ability to develop, implement and test robust security solutions. Key Accountabilities • Perform threat modeling and design security measures on complex applications and web-based products, • Desing and implement advanced operating system hardening, • Design and implement basic networking protections such as VPNs and tunneling, • Design advanced hardening configuration of cloud solutions, • Design simple cryptography-based solutions for data privacy and integrity protection Networking/Key relationships A cybersecurity engineer interacts with different stakeholders including: • Software development to plan and execute security and privacy by design activities, • Quality assurance to plan and execute cybersecurity testing across the product life-cycle, • Service to respond to on-market cybersecurity events impacting the company's products Minimum Knowledge & Experience required for the position: The qualifications required by the position are: • Engineer, computer science or other technical degree, or equivalent work experience The required work experience by the position is at least 4 years in one of the different tracks: • Ethical hacking and penetration testing, • Product security by design, • Cloud Security operations The following work experience and qualifications are a plus: • Strong knowledge of secure coding practices and product security best practices, • Certifications such as Certified Ethical Hacker (CEH), • Solid knowledge on SW testing process and methodology, • Knowledge on relevant standards such as ISO 27001, • Knowledge of medical device regulations Skills & Capabilities: The skills and capabilities required by the position are: • Strong analytical and problem-solving skills to identify and address security challenges and vulnerabilities, • Effective communication skills to convey complex cybersecurity concepts to both technical and non-technical stakeholders, • Willingness to stay updated on the latest cybersecurity trends, threats, and technologies through continuous learning and professional development, • Ability to collaborate with cross-functional teams, share information, and work together to enhance overall cybersecurity posture What we offer: • A meaningful project that will impact the quality of laboratory software medicine worldwide, • 3 days a week working from home, • Multicultural and friendly team, • Exciting opportunities for professional development., • Ongoing training, • Social benefits: Canteen, nursery check, continius training, Doctor at the office, retirement plan..., • All the benefits according to the chemical agreement Werfen appreciates and values diversity. We are an Equal Opportunity/Affirmative Action Employer M/F/D/V. Our Purpose: We contribute to the advancement of patient care around the world through innovative specialized diagnostics JOIN US!

Join Our Team as a Manufacturing Engineer at Multi-Wing in la Roca del Vallès, Catalonia, Spain. Are you passionate about transforming engineering designs into real, manufacturable products? Do you enjoy working at the intersection of design, production, and data accuracy? At Multi-Wing, we’re looking for a Manufacturing Engineer to help bridge the gap between product design and production — ensuring our world-class airflow solutions are built with precision and efficiency. 🚀 What You’ll Do As part of our Engineering team, you’ll: • Create and maintain product codifications, Bills of Materials (BoMs), and routings in Microsoft Dynamics 365., • Ensure manufacturing data is always accurate, consistent, and aligned with approved drawings and standards., • Collaborate closely with Design, Planning, Production, and Quality to release new products into manufacturing., • Execute and document engineering changes (ECN/ECO), ensuring timely updates across systems., • Support data governance, monitor master-data quality, and drive continuous improvement in processes and standards. This role is perfect for someone who thrives on precision, loves structure, and enjoys turning complex product data into clear, reliable manufacturing information. 🔧 What We’re Looking For • Education: BSc/MSc in Mechanical, Industrial, or Management Engineering (or equivalent)., • (A technical diploma with hands-on experience in manufacturing will also be considered.), • Experience:, • Entry-level candidates with internships/traineeships in manufacturing are welcome., • 1–3 years of experience in manufacturing engineering or master-data management (BoMs, routings) is a plus., • Skills:, • Strong understanding of production cycles, BoMs, and technical drawings., • Accuracy-focused, analytical, and comfortable with data-driven problem solving., • Advanced Excel skills and experience with ERP systems (preferably Microsoft Dynamics 365)., • Solid communication and documentation habits in a cross-functional environment., • Languages:, • English and Spanish – working proficiency (B2+). 💡 Nice to Have • Exposure to Lean / Continuous Improvement principles., • Familiarity with ECN/ECO processes and master-data quality KPIs., • Knowledge of variant/configuration management and data validation tools (e.g., Power Query, SQL). 🌍 Why Join Multi-Wing? At Multi-Wing, we’re proud to design and manufacture customized axial fans that help shape a more energy-efficient world. Joining us means becoming part of a global engineering community that values innovation, precision, and teamwork. You’ll have the opportunity to grow your technical expertise, contribute to process excellence, and make a visible impact in a dynamic, international manufacturing environment. 👉 Ready to take the next step? Apply now and help us drive excellence from design to production.

Noucor, con sede en Palau de Plegamans, Barcelona, es una compañía químico-farmacéutica española con un negocio centrado en I+D, licencia, fabricación y suministro de productos farmacéuticos. En Noucor contamos con un amplio conocimiento y experiencia en ofrecer productos y soluciones de calidad en el ecosistema de la salud a nivel mundial. Nuestra cultura promueve la confianza y la transparencia y apuesta por un nuevo liderazgo flexible y motivador. Seguimos construyendo una organización en la que la experiencia de las personas es un medio de compromiso, atracción y desarrollo del talento, para las personas sean siempre nuestro foco y prioridad. En esta ocasión, buscamos una persona para hacer prácticas en el departamento de Quality Assurance. ¿Te apuntas? ¿Qué funciones harás? • Dar soporte en la gestión del sistema de Calidad y la documentación GMP (PNTS, CAPAs, OOS, Desviaciones, Reclamaciones, etc), • Recopilar la información a incluir en los PQRs generada por los diversos departamentos GMP relevantes., • Redactar los informes PQRs (Product Quality Review)., • Evaluar mediante la estadística el estado de control de los procesos. ¿Qué perfil buscamos? • Estás cursando un grado de Ciencias de la Salud, Farmacia, Biociencias, Química o similares., • Nivel alto de inglés (C1) ¿Qué ofrecemos? ⚙️Trabajarás dentro de un gran equipo de profesionales con muy buen ambiente laboral. 🚀Tendrás aprendizaje y desarrollo continuo. 📍Vacantes tanto en las oficinas de Palau como de Sant Fost de Campsentelles. 💼Convenio de 1 año de duración. 🕒6 horas en turno de mañana. 🌱Servicio de comedor y transporte subvencionado. 🧘🏻 ♀️Nos preocupamos por tu Bienestar – el Plan Wellness incluye fisioterapia, psicología online, eventos deportivos, entre otros. En Noucor creemos en el poder de los equipos diversos. Por eso, valoramos todas las candidaturas sin distinción de género, edad, origen, orientación sexual, identidad de género o cualquier otra condición. Si te interesa aportar tu granito de arena al ecosistema de la salud y al bienestar de las personas, esta es tu oportunidad, no lo dudes, ¡te estamos esperando!

Technical Packaging Support – Granollers, Spain (12-Month Contract) Location: Granollers, Spain Contract Type: 12 months (with possibility of extension) Working Hours: Flexible – Monday to Thursday 9:00–18:00, Friday 9:00–15:00 Start Date: ASAP About Reckitt At Reckitt, we create products that make a real difference in people’s lives. From world-class Air Care, Surface, Laundry, and Pest Control products, our purpose is to Make a House Your Home. We are a high-energy, inclusive, and entrepreneurial team, shaping a culture that values curiosity, collaboration, and innovation. With trusted brands such as Air Wick, Cillit Bang, Calgon, and Mortein, joining Reckitt means contributing to products that people rely on every day, while growing your skills in a dynamic global company. The Role We are looking for a Technical Packaging Support professional to join our Granollers team. In this role, you’ll support the development, testing, and implementation of packaging solutions that ensure product quality, efficiency, and sustainability. You will work closely with cross-functional teams, suppliers, and production units to deliver packaging projects that meet technical and regulatory requirements. This role is ideal for someone who enjoys a hands-on, detail-oriented role and wants to contribute to innovative, high-quality packaging solutions in a fast-paced environment. Key Responsibilities • Collaborate with stakeholders to define and execute packaging projects on time and within scope., • Plan, conduct, and analyse packaging tests to ensure compliance with corporate standards., • Document packaging specifications and Bills of Materials (BOMs) in PLM systems and local databases., • Participate in innovation sessions, cost-saving programs, and continuous improvement initiatives., • Support supplier visits, quality investigations, and store checks., • Resolve packaging-related issues with production and quality teams., • Ensure compliance with legal, corporate, and ethical standards in packaging and supplier interactions., • Provide administrative support for sample management, storage, shipments, and document organization. What We’re Looking For Essential: • Degree in Engineering (Packaging, Mechanical, Chemical, or Materials preferred), • 1–2 years of experience in a similar role, • Fluent Spanish and intermediate English (B1–B2), • Proficiency in MS Office (Excel, Word, PowerPoint), • AutoCAD or packaging technology training Why Join Reckitt? • Flexible working hours and hybrid-friendly environment, • Competitive salary with medical insurance, • Free meals at the company canteen, • Discounts at wellness and sports centres, • Work in a high-growth, learning-focused project with a global impact Apply Now!!

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Immunoassay business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Within a medical device environment, work with the QARA Manager to ensure regulatory compliance and certification of software products. Key Accountabilities Be a key part of a team where you will: • Collaborate in maintaining the quality system documentation processes and procedures adopted by the company., • Investigate and resolve quality issues, implementing corrective and preventive actions to mitigate recurrence., • Coordinate and support the preparation of software technical documents appropriate for regulatory submissions., • Support the regulatory submissions for market authorization for medical device products., • Conduct internal assessments and audits to identify areas for improvement and ensure adherence to established procedures., • Facilitate the approval process for software releases., • Disseminating knowledge about the Quality System and regulatory requirements., • Review Promotional and advertising materials., • Oversee post-market surveillance activities related to medical device products., • Offer guidance and mentorship to QARA team members at lower levels Networking/Key relationships The main relationships within to the Werfen Group are: • QARA Manger, QA Leads, Validation Led, • Factory Lead and Solution Leaders, • Customer, • Application Lifecycle manager (ALM), • Notified Bodies and Competent Authorities for product regulatory compliance., • This position may also require also cooperating with other companies inside Werfen. Minimum Knowledge & Experience required for the position: • Engineer, computer Science or other Technical carrier, or equivalent work experience., • A minimum of 3 years experience in Quality Assurance or Regulatory related, preferably within the Healthcare sector, • Additional Skills/Knowledge:, • Knowledge and experience working with medical device international regulations and related standards (ISO 13485, ISO 14971,..)., • Knowledge and experience working in Medical device software life cycle process (IEC 62304), • Desirable:, • Knowledge and experience working in medical device regulatory submissions (MDR/IVDR,FDA..), • Internal auditor qualification for management systems or knowledge of auditing techniques Skills & Capabilities: The ideal candidate for this position will exhibit the following skills and competencies: • Good level of Technical and Conversional English., • Team player with ability to work independently., • Excellent and effective written and verbal communication skills., • Excellent interpersonal skills, good judgment and analytical skills., • Effective time management and organizational skills What we offer: • A meaningful project that will impact the quality of laboratory software medicine worldwide, • 3 days a week working from home, • Multicultural and friendly team, • Exciting opportunities for professional development., • Ongoing training, • Social benefits: Canteen, nursery check, English training..., • All the benefits according to the chemical agreement Our Purpose: We contribute to the advancement of patient care around the world through innovative specialized diagnostics JOIN US!

En esta ocasión, buscamos una persona para hacer prácticas en el departamento de Quality Assurance. Redactar los informes PQRs (Product Quality Review).

Technical Packaging Support – Granollers, Spain (12-Month Contract) Contract Type: 12 months (with possibility of extension) Working Hours: Flexible – Monday to Thursday 9:00–18:00, Friday 9:00–15:00 Start Date: ASAP From world-class Air Care, Surface, Laundry, and Pest Control products, our purpose is to Make a House Your Home. We are a high-energy, inclusive, and entrepreneurial team, shaping a culture that values curiosity, collaboration, and innovation. With trusted brands such as Air Wick, Cillit Bang, Calgon, and Mortein , joining Reckitt means contributing to products that people rely on every day, while growing your skills in a dynamic global company. We are looking for a Technical Packaging Support professional to join our Granollers team. In this role, you’ll support the development, testing, and implementation of packaging solutions that ensure product quality, efficiency, and sustainability. You will work closely with cross-functional teams, suppliers, and production units to deliver packaging projects that meet technical and regulatory requirements. This role is ideal for someone who enjoys a hands-on, detail-oriented role and wants to contribute to innovative, high-quality packaging solutions in a fast-paced environment. Collaborate with stakeholders to define and execute packaging projects on time and within scope. Plan, conduct, and analyse packaging tests to ensure compliance with corporate standards. Document packaging specifications and Bills of Materials (BOMs) in PLM systems and local databases. Support supplier visits, quality investigations, and store checks. Resolve packaging-related issues with production and quality teams. Ensure compliance with legal, corporate, and ethical standards in packaging and supplier interactions. Degree in Engineering (Packaging, Mechanical, Chemical, or Materials preferred) ~Fluent Spanish and intermediate English (B1–B2) ~ Proficiency in MS Office (Excel, Word, PowerPoint) ~ AutoCAD or packaging technology training Flexible working hours and hybrid-friendly environment Competitive salary with medical insurance Work in a high-growth, learning-focused project with a global impact

Technical Packaging Support – Granollers, Spain (12-Month Contract) Contract Type: 12 months (with possibility of extension) Working Hours: Flexible – Monday to Thursday 9:00–18:00, Friday 9:00–15:00 Start Date: ASAP From world-class Air Care, Surface, Laundry, and Pest Control products, our purpose is to Make a House Your Home. We are a high-energy, inclusive, and entrepreneurial team, shaping a culture that values curiosity, collaboration, and innovation. With trusted brands such as Air Wick, Cillit Bang, Calgon, and Mortein , joining Reckitt means contributing to products that people rely on every day, while growing your skills in a dynamic global company. We are looking for a Technical Packaging Support professional to join our Granollers team. In this role, you’ll support the development, testing, and implementation of packaging solutions that ensure product quality, efficiency, and sustainability. You will work closely with cross-functional teams, suppliers, and production units to deliver packaging projects that meet technical and regulatory requirements. This role is ideal for someone who enjoys a hands-on, detail-oriented role and wants to contribute to innovative, high-quality packaging solutions in a fast-paced environment. Collaborate with stakeholders to define and execute packaging projects on time and within scope. Plan, conduct, and analyse packaging tests to ensure compliance with corporate standards. Document packaging specifications and Bills of Materials (BOMs) in PLM systems and local databases. Support supplier visits, quality investigations, and store checks. Resolve packaging-related issues with production and quality teams. Ensure compliance with legal, corporate, and ethical standards in packaging and supplier interactions. Degree in Engineering (Packaging, Mechanical, Chemical, or Materials preferred) ~Fluent Spanish and intermediate English (B1–B2) ~ Proficiency in MS Office (Excel, Word, PowerPoint) ~ AutoCAD or packaging technology training Flexible working hours and hybrid-friendly environment Competitive salary with medical insurance Work in a high-growth, learning-focused project with a global impact

Technical Packaging Support – Granollers, Spain (12-Month Contract) Contract Type: 12 months (with possibility of extension) Working Hours: Flexible – Monday to Thursday 9:00–18:00, Friday 9:00–15:00 Start Date: ASAP From world-class Air Care, Surface, Laundry, and Pest Control products, our purpose is to Make a House Your Home. We are a high-energy, inclusive, and entrepreneurial team, shaping a culture that values curiosity, collaboration, and innovation. With trusted brands such as Air Wick, Cillit Bang, Calgon, and Mortein , joining Reckitt means contributing to products that people rely on every day, while growing your skills in a dynamic global company. We are looking for a Technical Packaging Support professional to join our Granollers team. In this role, you’ll support the development, testing, and implementation of packaging solutions that ensure product quality, efficiency, and sustainability. You will work closely with cross-functional teams, suppliers, and production units to deliver packaging projects that meet technical and regulatory requirements. This role is ideal for someone who enjoys a hands-on, detail-oriented role and wants to contribute to innovative, high-quality packaging solutions in a fast-paced environment. Collaborate with stakeholders to define and execute packaging projects on time and within scope. Plan, conduct, and analyse packaging tests to ensure compliance with corporate standards. Document packaging specifications and Bills of Materials (BOMs) in PLM systems and local databases. Support supplier visits, quality investigations, and store checks. Resolve packaging-related issues with production and quality teams. Ensure compliance with legal, corporate, and ethical standards in packaging and supplier interactions. Degree in Engineering (Packaging, Mechanical, Chemical, or Materials preferred) ~Fluent Spanish and intermediate English (B1–B2) ~ Proficiency in MS Office (Excel, Word, PowerPoint) ~ AutoCAD or packaging technology training Flexible working hours and hybrid-friendly environment Competitive salary with medical insurance Work in a high-growth, learning-focused project with a global impact

We are a Spanish manufacturing company specialised in PET blow-moulding machinery, located in Granollers area (near Barcelona). With customers worldwide, we are a reference in our sector thanks to our innovative solutions and an excellent team of professionals. As part of our growth, we are looking to incorporate a Mechanical Technician / Assembler & Fitter to join our team, reporting directly to the After-Sales Service Manager. We are seeking a skilled professional capable of performing precision mechanical assembly and fine adjustments for new machinery, as well as providing after-sales support. Main responsibilities • Mechanical assembly, installation, commissioning and maintenance of machines at customer sites., • Assembly and commissioning of machines in our manufacturing workshop., • Ensuring machine quality according to company standards., • Preparation of technical reports. Approximately 50% of the time will involve travelling. When not travelling, you will support the technical assembly team in the workshop. What We Offer • A solid and well-established company., • Permanent employment contract (with trial period)., • Workshop schedule: Monday to Friday, 6:00–14:00., • When working at customer sites, hours will adapt to customer requirements and additional compensation will be provided., • Job stability and long-term continuity., • Continuous training., • All travel expenses covered by the company., • Daily allowances for customer-site travel., • Company vehicles available for travel to customer facilities., • Formal training in Mechanical Engineering / Mechanics., • Minimum 4 years of experience as a mechanical assembler/fitter of industrial machinery., • Strong ability to interpret 2D technical drawings., • Valid driving licence (Spain)., • Availability to travel 50% (national and international)., • Sufficient English level to communicate with technical staff at international customer sites., • Preferably living near the Vallès Oriental area., • Base salary : €38,000 – €40,000 gross/year., • Including travel compensation (approx. 50% of the time), annual earnings may exceed €60,000 gross/year.

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. The Senior SW Development Engineer, develop a role as as either full-stack or front-end or back-end , being involved in all stages and all areas of software development, including Test as well as architecture design, code review, and internal tool management. The programming language required for this project is Standard C++ They are responsible for developing and implementing front-end and/or back-end software applications, including back-end design, testing, and systems integration. Performs software engineering activities including software requirements, architecture, design, implementation and test independently. Lead software development activities within projects at technical or at project level. Able to complete somewhat ambiguous problems and defect fixing with its corresponding test. Works across the-full stack, or focused in back-end or front-end, building scalable solutions that drive positive user experiences and measurable business impact Develops new software features and infrastructure elements in support of priority business and solution requirements. Ensures application performance, uptime, risk mitigation, scalability, and high code/application quality Uses agile engineering practices and various software development technologies to rapidly develop creative and efficient solutions that enhance the organization’s technology stack Collaborates with other squad members to implement user stories, write tests, and continuously deliver new/improved product functionality. Will design and build software that is simple and scalable. Will know your project in a low complexity level, enough to cover your work autonomously and the environment where it works with some detail. Will work in a project with low or medium complexity Will able to work autonomoslly, however you know when you have to consult the experts on the issues that appear on the projects Could act as a Scrum master of the project Engineer, computer Science or other Technical degree, or equivalent work experience Experience in Software Medical Devices development that follows ISO 13485 is a plus Proficient in all the languages and frameworks used in the project Proficient in Database Queries and Database Design Sound problem-solving skills with the ability to quickly process complex information and present it clearly and simply A meaningful project that will impact the quality of laboratory software medicine worldwide ~3 days a week working from home ~ Exciting opportunities for professional development. ~ Ongoing training ~ Social benefits: Canteen, nursery check, continius training, Doctor at the office, retirement plan... ~

Redactar los informes PQRs (Product Quality Review).

Empresa especializada en elaboración de productos dietéticos y dietoterápicos, busca incorporar un Responsable de QA y Regulatory con experiencia en laboratorios de suplementación, alimentación, medicamentos y/o bebidas.Su objetivo es liderar los subdepartamentos de QA y Regulatory para garanti

Redactar los informes PQRs (Product Quality Review).

Delegar funciones del Quality & Env Manager cuando sea necesario.

Redactar los informes PQRs (Product Quality Review). En esta ocasión, buscamos una persona para hacer prácticas en el departamento de Quality Assurance.

Empresa especializada en elaboración de productos dietéticos y dietoterápicos, busca incorporar un Responsable de QA y Regulatory con experiencia en laboratorios de suplementación, alimentación, medicamentos y/o bebidas.Su objetivo es liderar los subdepartamentos de QA y Regulatory para garanti

En esta ocasión, buscamos una persona para hacer prácticas en el departamento de Quality Assurance. Redactar los informes PQRs (Product Quality Review).

Desde Paul Marlex colaboramos con una compañía industrial ubicada cerca de Polinyà, dedicada a la fabricación y transformación de productos químicos, en la búsqueda de un/a Responsable de Calidad para reforzar su equipo.Tu misión Serás la persona referente del área de calidad, impulsando l

Desde Paul Marlex colaboramos con una compañía industrial ubicada cerca de Polinyà, dedicada a la fabricación y transformación de productos químicos, en la búsqueda de un/a Responsable de Calidad para reforzar su equipo.Tu misión Serás la persona referente del área de calidad, impulsando l

Quality Control en el Turno de Tarde.

Desde Paul Marlex colaboramos con una compañía industrial ubicada cerca de Polinyà, dedicada a la fabricación y transformación de productos químicos, en la búsqueda de un/a Responsable de Calidad para reforzar su equipo.Tu misión Serás la persona referente del área de calidad, impulsando l

Quality Control en el Turno de Tarde.

Desde Paul Marlex colaboramos con una compañía industrial ubicada cerca de Polinyà, dedicada a la fabricación y transformación de productos químicos, en la búsqueda de un/a Responsable de Calidad para reforzar su equipo.Tu misión Serás la persona referente del área de calidad, impulsando l

Quality Control en el Turno de Tarde.

Somos la firma global de talento: Selección, headhunting, formación y consultoría de Eurofirms Group.En Claire Joster creemos en el talento único de cada persona y sabemos que la diversidad aporta valor a los equipos, impulsando organizaciones más innovadoras, creativas y eficientes.Por eso, co

En esta ocasión, buscamos una persona para incorporarse en el departamento de Quality Control en el Turno de Tarde.

About the Role Join HP's EMEA Service Supply Chain team and gain hands-on experience in quality and operations management! As a Quality and Operations Analyst Intern, you'll work on real-world projects that improve repair and refurbishment processes for HP printing products across Europe

In this role, you’ll be pivotal in ensuring compliance with Good Manufacturing Practices (GMP) through the validation of facilities, equipment, and processes as well as through the preparation of Quality Systems. Participating in quality assurance projects as writing procedures and work instructio

Support supplier quality management, including audits, evaluations, and establishing quality agreements. Junior Quality Engineer/Quality Technician". Develop, implement, and maintain quality control processes for manufacturing and maintaining machines.

Girona | 🔄 Contrato 1 año | 🧬 Sector Farmacéutico.Grupo Synergie, estamos colaborando con una organización del sector farmacéutico y biotecnológico, ubicada en el área de Girona, en la búsqueda de un/a.Si te motiva trabajar en un entorno.Formarás parte del equipo de Calidad, dando sopo

Experiencia en QA, Quality Systems o QA Operations dentro del sector farma. Conocimientos sólidos en GMP y manejo de Quality Events (deviations, CAPAs, CCs). ALTENSpain #LifeSciences #QualityAssurance #GMP #QAJobs #Pharma.

Solutia Life Sciences (división de reclutamiento de Solutia) se especializa en perfiles técnicos y mandos intermedios en los sectores farmacéutico, biotecnológico y de dispositivos médicos.Desde Solutia Life Sciences buscamos un líder apasionado por la calidad y las personas para asumir el rol

You will be responsible for the quality system of the sales office in Barcelona as well as supporting the registrations for Spain. Furthermore, you are part of the EMEA Quality Assurance and Regulatory affairs team, for this region you will be responsible for collecting clinical data from surgeons t

Scientist for Biologics Quality Control. The design, supervision and execution of quality control studies of Biological Products including. Knowlegde of electrophoretic techniques, Western-Blot and ELISAs and Quality Control of Proteins will be a plus.

Liderar el equipo de Calidad del centro de producción, incluyendo Quality Management (QM), Quality Control (QC) y Regulatory Affairs. Quality Manager | Medical Devices.

At least 2 years of experience in software or ML quality assurance, including functional, performance, and automation testing. A Quantum Computing & AI software company based in Zaragoza are seeking to bolster their team with a Quality Control engineer. Assess system quality across diverse operating

This person will foster an organizational culture where quality is a shared value, anticipating risks and generating a positive impact, and will integrate the quality strategy with sustainability to reinforce our position as a benchmark in health, nutrition, and trust. Quality & Food Safety Director

Conocimientos sólidos en GMP y manejo de Quality Events (deviations, CAPAs, CCs). ALTENSpain #LifeSciences #QualityAssurance #GMP #QAJobs #Pharma. Asegurar el cumplimiento de requisitos GxP y estándares de Quality Compliance.

Quality Control, Quality Assurance & Continuous Improvement. The Director of Quality and Regulatory Affairs will play a central role in defining and executing the organization’s overall quality and regulatory roadmap. This position oversees the Quality Control, Quality Assurance, and Regulatory Af

Girona | 🔄 Contrato 1 año | 🧬 Sector Farmacéutico.Grupo Synergie, estamos colaborando con una organización del sector farmacéutico y biotecnológico, ubicada en el área de Girona, en la búsqueda de un/a.Si te motiva trabajar en un entorno.Formarás parte del equipo de Calidad, dando sopo

Desde HAYS Life Sciences nos encontramos en búsqueda de DOS perfiles técnicos para empresa de la industria farmacéutica en la zona del Vallès Oriental.OTCs (cosméticos / complementos alimenticios).GMP y gestión de la calidad en industria farmacéutica.TÉCNICO/A EN ASUNTOS REGULATORIOS:.Elabor

Solutia Life Sciences (división de reclutamiento de Solutia) se especializa en perfiles técnicos y mandos intermedios en los sectores farmacéutico, biotecnológico y de dispositivos médicos.Desde Solutia Life Sciences buscamos un líder apasionado por la calidad y las personas para asumir el rol

Guarantee the quality and operational reliability of AI solutions across multiple deployments. Establish and standardize quality control processes and reporting across all projects. Serve as a key point of contact for quality validation, ensuring final deliverables meet the highest technical and fun

Scientist for Biologics Quality Control. The design, supervision and execution of quality control studies of Biological Products including. Knowlegde of electrophoretic techniques, Western-Blot and ELISAs and Quality Control of Proteins will be a plus.