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International Sales Area Manager International Role | Medical Devices | Hybrid Work | Fast-Growing Team ___ is an innovative technological company dedicated to the development and commercialization of medical devices in the fields of neuro, spinal and cardiac surgery. Offices based in Cerdanyola del Valles (Barcelona).Their mission is to provide worldwide surgeon with innovative solutions. As Sales Area Manager, you will be responsible for driving business growth in assigned territories, managing distributor relationships, and supporting the adoption of their innovative products in hospitals across the globe. You will work closely with surgeons and distributors, combining sales drive with hands-on product application support. This is an exciting opportunity to join a small but highly dynamic team and where your work will have direct impact on our growth. Your Role & Responsibilities: • Build and maintain strong relationships with distributors, creating added value through business growth., • Manage the full sales cycle in your assigned territories: from identifying opportunities and negotiating contracts to closing deals., • Support distributors with joint hospital visits, sales model reviews, product trainings, and assistance during surgeries., • Travel occasionally to meet clients, attend congresses, and represent NEOS Surgery internationally., • Identify new sales channels, expand distributor databases, and support overall business development., • Stay ahead of industry trends: analyse competitors, benchmark the market, and share insights with the team., • Collaborate closely with Marketing, Clinical, R&D, Quality, and Regulatory departments., • Master our product portfolio and work hand-in-hand with our product specialist to resolve customer queries., • Co-create marketing tools and solutions tailored to specific customer needs. What We’re Looking For: • Degree in Life/Health Sciences, Economics, or Business Administration., • 2–4 years of professional experience, ideally in the medical device sector., • Strong ambition to develop a career in business development and sales., • Previous commercial/sales experience is a plus, but not essential., • Fluent English, • Willingness to travel internationally Why Join NEOS Surgery? • Be part of a young, dynamic, and ambitious team where entrepreneurship and initiative are valued., • Work in the fast-growing medical devices sector with an international presence in 20+ countries., • Experience a flexible and hybrid work environment, designed to empower high performance and personal growth., • Join a company on the rise, where you will have real impact and grow alongside the business.

Automation Engineer For our Grifols in Parets, we are looking for an Automation Engineer. This is a key hire for the successful implementation of a newly introduced equipment. We are seeking a professional with strong expertise and proven technical leadership skills. Main Requirements: • Minimum of 5 years of experience in industrial automation projects., • Advanced knowledge of Siemens TIA Portal and Siemens AWL Step7., • Hands-on experience with the commissioning of new machines/lines, troubleshooting, and process validation., • Desirable: knowledge of Rockwell and Zenon SCADA systems. Additional Skills (highly valued for this project): • Experience in the integration of equipment within GMP/pharma or other highly regulated environments., • Ability to prepare technical documentation and contribute to qualification processes (IQ/OQ)., • Strong team-player mindset to collaborate across engineering, maintenance, production, and quality teams., • Excellent problem-solving, analytical skills, and ability to liaise with external suppliers. This role will be essential in ensuring the successful start-up, optimization, and validation of the new machine, bringing expertise in both programming and systems integration. 📍 Location: Parets (Barcelona Area) Travelling may not be requiered at the begining but we need flexible travelling according the project is moving on -international-.

Desde Claire Joster Recruitment estamos en búsqueda de un/a PRODUCTION SPECIALIST para unirse a una compañía farmacéutica internacional de referencia: Esteve Química. Esteve Química es una empresa líder en el sector farmacéutico en España, con fuerte presencia internacional. Su compromiso con la innovación, la investigación y las alianzas estratégicas la convierten en un referente en la fabricación de ingredientes activos farmacéuticos (APIs) y productos intermedios. Con sede central y centro de I+D en Barcelona, cuenta con plantas de producción en Celrà, Lliçà de Vall y Banyeres del Penedès. La posición está ubicada en la planta de producción de Lliçà de Vall. Tu misión será dar soporte técnico, documental y formativo al Responsable de Producción en aquellas tareas que así se requiera en la planta. Tus principales responsabilidades incluirán: • Proponer soluciones y mejoras industriales de los procesos en la planta de LDV., • Seguimiento y soporte en la puesta en marcha de los nuevos procesos de producción., • Soporte técnico-administrativo al Responsable de Producción., • Soporte en la ejecución de las campañas industriales, teniendo en cuenta la planificación establecida por el Responsable de Producción y los Industrial Process Leaders (IPL)., • Formación del personal de planta de producción en nuevos procesos y operativas. -Participar en la elaboración de HAZOP de los procesos. • Preparación de Quality Risk Assessment de los procesos, entre otros documentos., • Colaborar en los traspasos de procesos desde y hacia otros centros de trabajo nacionales e internacionales., • Dar soporte técnico en auditorías e inspecciones de clientes y autoridades., • Back-up del jefe de turno en su ausencia. -Detectar, proponer e implantar mejoras en los procesos químicos de producción. -Redactar Hojas de fabricación, Hojas de limpieza y toda aquella documentación que proceda. -Preparar controles de cambios. -Preparar desviaciones de proceso. -Preparación y cumplimentación de documentación técnica de instalaciones (Protocolos, Cualificaciones). • Detectar y proponer soluciones a las necesidades de producción en relación a la mejora de equipos/instalaciones, inversiones, formación, Prevención y Medio Ambiente, etc. Requisitos: • Licenciatura en Ciencia Químicas o Ingeniería Química., • Catalán y Castellano., • Inglés nivel B2 (según MRCE)., • Experiencia en puesto similar en planta de producción, preferiblemente en el sector químico-farmacéutico. Formación complementaria en: • Cursos Normativa GMPs para APIs., • Cursos de Prevención y Medioambiente., • Office usuarios. Se ofrece: • Contrato temporal, aproximadamente de 20 semanas., • Beneficios sociales: subsidio de comedor, seguro colectivo, pluses adicionales., • Horario de turno continuo: mañana-tarde-noche, de lunes a viernes., • Salario competitivo. ¿Te interesa o conoces a alguien que encaje? ¡No dudes en compartir o aplicar!

At Werfen, a global leader in in-vitro diagnostics, we are looking for a Technical Support Scientist to join our OEM Operations team. This role is ideal for a scientifically minded professional who enjoys designing experiments, analyzing data, and collaborating across functions in a highly regulated, quality-driven environment. About the Role As a Technical Support Scientist, you will perform a broad range of technical and analytical activities to ensure the optimal performance of our diagnostic products. You will provide specialized scientific and technical support to Production, R&D, and Quality Control teams, contributing to product improvement, troubleshooting, and the successful transfer of new products from development to manufacturing. Note: This position focuses on experiment design, data analysis, and interpretation. Hands-on laboratory testing will be executed by technicians, although strong laboratory knowledge is required. What You’ll Do • Design experiments and define appropriate analytical or experimental methods for specific projects., • Analyze, interpret, and draw conclusions from experimental and performance data., • Investigate deviations, identify potential issues, and propose corrective actions., • Prepare and present results and technical reports to senior staff., • Write and review laboratory procedures and documentation in compliance with GMP and ISO standards., • Support activities related to Non-Conformities (NCs), CAPAs, and continuous improvement projects., • Participate actively in Lean Six Sigma and 5S initiatives., • Bachelor’s degree in Biology, Biochemistry, Biotechnology, or a related scientific field., • (A higher degree or equivalent experience is an advantage.), • Experience in a laboratory environment, ideally within a regulated setting (GMP, ISO 13485, FDA)., • Strong knowledge of biological and chemical laboratory techniques and diagnostic products (IBDR)., • Familiarity with MS Office; SAP experience is a plus., • Fluent in Spanish or Catalan, with advanced English skills (written and spoken)., • Strong analytical mindset, attention to detail, and problem-solving skills. At Werfen, you’ll join a collaborative, innovation-driven culture where science meets purpose. You’ll work with talented colleagues across R&D, Quality, and Operations, contributing to products that have a real impact on patient care worldwide. Travel: Occasional short-term assignments to external labs may be required Ready to make an impact through science and technology? Apply now and become part of a global team advancing diagnostics and improving lives.

At Siegfried, we offer more than just a job — we provide a platform for you to thrive, grow, and shape your future. With locations across the globe, we empower our employees to build meaningful, international careers in a truly dynamic and collaborative environment. We believe in the power of multidisciplinary teamwork and encourage every individual to take ownership of their personal and professional development. At Siegfried, your ideas matter, your voice is heard, and your contribution drives real impact. Our culture of innovation, continuous learning, and shared success makes Siegfried not just a workplace — but a place where you can growth professionally. Your Role: • Technical and functional consultant for Data Intelligence, including the implementation of reporting and analytics solutions in the SAP BW/4HANA and SAP Analytics Cloud environments (SAP Datasphere and SAP Analytics Cloud Planning as a plus)., • Translate business needs and design scalable, compliant Data Intelligence solutions by implementing roadmaps, ensuring end-to-end consistency and auditability across all Siegfried sites., • Design and govern scalable Data Intelligence solutions with the focus on reporting and analytics based on standards to ensure quality, compliance, and consistency across Siegfried's business areas., • Support evaluation of the new reporting and analytics tools (SAP Business Data Cloud, SAP DataSphere, SAP Analytics Cloud for Excel, and others)within data intelligence area to ensure reusability, compliance, and fit-for-purpose solutions., • Coordination and management of external consulting resources in term of project and resource management, • Conduct internal trainings on data intelligence (reporting/analytics), promoting best practices and knowledge sharing. Your Profile: • Educational background in Information Technology or equivalent qualification., • At least 10 years of previous experience in a similar role., • Proven project and hando-on expertise in reporting and analytics, predominantly within the SAP environment., • Proven experience in delivering services related to data extraction, data modelling, and building highly appealing user interfaces, • Experience with Data Management solutions (e.g., MDG, ILM) or SAP Industry Solutions is an added advantage, • Experience with programming languages like ABAP, AMDP, and JavaScript is a plus, • Solution-oriented personality with strong communication skills., • Willingness to work on a broad range of topics around Data Intelligence, • Resilient team player with high flexibility., • Fluent in Spanish and English, both written and spoken.

About Werfen Werfen is a global leader in specialized diagnostics, operating directly in over 30 countries and reaching more than 100 territories worldwide through distributors. We develop, manufacture, and distribute integrated solutions — including systems, reagents, automation, and software — for use primarily in hospitals and clinical laboratories. At Werfen, we are driven by innovation, precision, and collaboration. Our people are at the heart of everything we do, committed to advancing patient care through excellence in science and technology. What You’ll Be Doing: As a Maintenance Technician, you will be responsible for repairing and installing manufacturing and R&D equipment, ensuring all systems operate efficiently and safely. You will perform preventive maintenance according to manufacturer specifications, inspect equipment performance, and diagnose and correct malfunctions or technical issues as needed. Key Responsibilities: • Perform preventative maintenance on the assigned equipment, • Repair all production equipment as needed, • Perform breakdown analysis, • Perform general housekeeping, • Upgrade production lines with new equipment/technology, • Work with outside contractors working on assigned line, • Comply with GMP, safety, and audit standards, • Work independently under limited supervision (self-management), • Documentation of the work orders, • Collaborate on the improvements and optimization of the machines Networking/Key relationships: This position requires cooperation with: • Filling & Packaging Department, • Bulk and Intermediate Manufacturing Departments, • Engineering Minimum Knowledge & Experience required for the position: • Education: • Required: CFGM in maintenance, Mechanics, electronic, electric, or similar. Valuable: Any additional degree higher than that required in the previous section • Experience: • Depending on the type of laboratory to which the technician is going to be placed, specific experience may be required in topics like maintenance, Mechanics, electronic, electric. • Additional Skills/Knowledge • Software: Fluency in Office Tools (Excel & Word), and valuable basic knowledge in SAP., • Language: Fluency in Spanish or Catalan. Basic knowledge of English (reading and, • speaking). Skills & Capabilities: The ideal candidate for this position will exhibit the following skills and competencies: • Ability to maintain, calibrate and use technical equipment with accuracy, • Flexibility in order to work with and provide support for a number of people, • Teamwork, • Attention to detail, • Oral and written communication skills, • Reflects company values through the quality of work and professional relationships.

About Werfen Werfen is a global leader in specialized diagnostics, operating directly in over 30 countries and reaching more than 100 territories worldwide through distributors. We develop, manufacture, and distribute integrated solutions — including systems, reagents, automation, and software — for use primarily in hospitals and clinical laboratories. At Werfen, we are driven by innovation, precision, and collaboration. Our people are at the heart of everything we do, committed to advancing patient care through excellence in science and technology. What You’ll Be Doing: As a Manufacturing Lab Technician, you’ll support the execution of manufacturing processes while ensuring compliance with quality, safety, and environmental standards. You’ll prepare materials, reagents, and equipment, carry out laboratory procedures and tests, record production data, and perform routine maintenance of lab instruments. Key Responsibilities: • Conducts manufacturing processes and laboratory tests according to approved instructions., • Operates a variety of laboratory equipment, • Compiles manufacturing data, performs the required calculations and complete the corresponding manufacturing and testing records., • Maintains a clean, sanitary and well resourced work area in accordance with approved practices and the regulations in place., • Follow strict laboratory, quality, safety and environmental procedures according to regulations in place., • Under the supervision of his manager and with the support -if needed- of other colleagues, can collaborate in the transfer & set up of new processes and systems., • Participates in activities related to continuous improvement, 5S and Lean Six-Sigma Requirements: Education: Vocational training (Ciclo Formativo de Grado Medio or higher) in a science or health-related field. Experience: Previous work in laboratory environments is essential. Experience in cell culture, molecular biology, biochemistry, lab automation, or clinical analyzers will be a plus. Experience in chemical, biological, or health laboratories will be highly valued. Equivalent experience can be considered in place of formal education. Languages: Fluency in Spanish or Catalan and a basic level of English (reading and speaking). IT Skills: Confident user of Microsoft Office (Excel, Word). Basic knowledge of SAP will be considered an advantage. Skills & Competencies: • Strong ability to operate, calibrate, and maintain laboratory equipment accurately., • Attention to detail and precision in daily work., • Team-oriented and flexible, able to support colleagues across different areas., • Good communication skills, both written and verbal., • Commitment to quality, safety, and continuous improvement in all tasks.

The Siegfried Group is a global life science company with a network of 13 sites in Europe, the USA and Asia. Siegfried offers contract development and manufacturing of active pharmaceutical ingredients, intermediates, and drug products and has sales more than CHF 1.3 billion Swiss Franks. Siegfried Holding AG employs over 3,900 people and is listed on the SIX Swiss Exchange (SIX: SFZN). Are you a Senior Manager Business Applications (SAP Data Migration) looking for a new challenge in a dynamic CDMO Pharmaceutical Industry in our Barberà del Vallès site? Reporting to the Head Data Intelligence and SAP-Basis, you will be responsible for replacing the existing system to migrate data, selecting and evaluating data migration designs, governing scalable data migration architectures and standards across SAP programs. Your role: • Technical and functional lead for SAP data migration and master data projects, including architectural transition from R/3 (ECC 6.0) to the S/4HANA landscape., • Convert business needs and design scalable, compliant data migration solutions and roadmaps, ensuring end-to-end consistency and auditability across all Siegfried sites., • Design and govern scalable data migration architectures and standards to ensure quality, compliance, and consistency across SAP programs., • Select and evaluate data migration (e.g., SAP Data Services, LSMW) and master data tools to ensure reusability, compliance, and fit-for-purpose solutions., • Coordination and management of external consulting resources in term of project management, • Conduct internal trainings on data migration and master data, promoting best practices and knowledge sharing. Your profile: • Educational background in Information Technology or equivalent qualification., • Led at least one complex data migration project to SAP S/4HANA., • At least 7 years experience in delivering services related to data migration, transformation, and support for mergers, acquisitions, and divestitures, • Served as an enterprise architect or advisor, guiding customers in building IT roadmaps using SAP products and services., • Experience with Data Management solutions (e.g., MDG, ILM) or SAP Industry Solutions is an added advantage, • Experience with SQL is a plus., • Solution-oriented with strong communication skills., • Willingness to work on a broad range of topics in the area of SAP Master data ., • Resilient team player with high flexibility., • Fluent in Spanish and English, both written and spoken. Working at Siegfried Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs. Who we are In the Midst of People’s Lives – Across the Globe The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products.

Tucai Group is considered one of the leading manufacturers of flexible connection hoses and valves for gas, water, and fuel applications, with globally recognized certifications. The mission of the Customer Service role is to serve our national and international customers in their sales and after-sales activities and experience. THE ROLE Key responsibilities: • Insert customer orders in the ERP systems and manage order confirmations to customers., • Receive and respond to customer enquiries, emails and phone calls. Send invoices and shipment related documents. Send rappel reports to customers. Send samples, commercial documents, catalogues, etc., • Receive customer claims and insert them in the internal app. Transfer and manage with involved departments all information from customers and send back information to customers regarding the status of related claims. Manage credit and replacements., • Carry out the internal processes to ship orders to customers: send internal order to logistic dpt. when goods are produced and ready to be shipped. Work as a team and coordinate with our international plants., • Create and maintain updated customer files in ERP system, keep customer data permanently updated (customer contacts, shipping address, price list). Follow internal procedure to open new customers (Financial approval process and risk assignment), • Insert sales forecast received from customers into ERP system., • Negotiate with customers in case of incidents or needs. WE ARE LOOKING FOR A CANDIDATE WITH: • Middle degree in technical, economics, or any related field., • A minimum of 5 years’ experience in Customer Service within an international company., • Experience with EDI and/or Microsoft 365 or similar. Good command of Ms.Office., • Fluent English is a must for daily communication. French or another European language is a plus., • Willing to travel occasionally., • The role is for a very committed person with high standards of quality, a dynamic personality and a strong customer orientation., • Due to limited public transportation options, applicants must have a car. WHAT CAN WE OFFER YOU? • Full-time and permanent contract, • Flexible hours (7:30/9:15 to 16:30/18:30), short days on Fridays and in August., • You can work from home 1 or 2 days per week depending on your tasks and schedule., • Food vaucher and flexible benefits., • Salary according to experience and profile.

About the company: At Noucor we work on providing solutions to improve people's quality of life and contribute to a more sustainable world. We're a Spanish pharmaceutical company based in Barcelona and our business is focused on R+D, licensing, manufacturing, and the supply of pharmaceutical products. We have an extensive knowledge and experience offering quality products and solutions in the health ecosystem. We have an innovative focus with an industrial vocation with a fine chemical plant dedicated to the development and production of active pharmaceutical ingredients, a pharmaceutical plant manufacturing solid and semi-solid forms and a plant exclusively focused on food supplements. With 500 employees, we are present in over 100 markets being Japan, Canada and the EU key markets. Our culture promotes diversity, equality and inclusion and is committed to a new flexible and motivating leadership. We keep on building an organization in which people's experience is a means of engagement, attraction and development of talent, to always make people our focus and priority. Join the Legal Team at Noucor! We’re looking for a Legal Counsel. Are you ambitious and ready to take on a new challenge in a highly complex and responsible environment? If so, keep reading! Your challenges: • Participate in the negotiation of various types of contracts typical of the pharmaceutical industry, including drafting and reviewing confidentiality agreements, service agreements, licensing agreements, co-development, manufacturing and supply agreements, etc., • Provide legal advice to different areas of the company, such as Business Development, Clinical Affairs, Procurement, Regulatory Affairs, Marketing, and others., • Carry out administrative tasks, such as attending notary appointments and filing documents in the repository. What are we looking for? • Education: A degree in Law., • Experience: At least two years of experience in the legal department of a pharmaceutical company or a law firm advising companies in the sector., • Language skills: Professional proficiency in English, both spoken and written, is essential., • Profile: Enthusiasm for working in a multinational and innovative company. Passion for legal matters in international projects. We Offer: 🤩 Work within a great team of professionals with a very good work environment. ⚙️ Innovative work environment focused on continuous improvement. 🚀 Continuous learning and development. 💼 Competitive benefits package and flexible schedule. 📍 Offices in Palau-solità i Plegamans. 💰 Competitive salary. If this sounds like you, don’t miss the chance to embark on this exciting opportunity!

Role Summary We are looking for a motivated and detail-oriented professional to support the development of international sales for consumables within companies of the same group. The selected person will manage the full sales cycle — from preparing quotations to building lasting client relationships — ensuring high service quality and consistent results. Main Responsibilities • Prepare, manage and follow up on quotations and commercial offers., • Negotiate terms and agreements with international suppliers and clients., • Coordinate the complete sales and after-sales process., • Develop and implement commercial strategies focused on results., • Build and maintain long-term relationships with clients through excellent service., • Prepare presentations, proposals and tailor-made solutions for each opportunity., • Support international projects and monitor their progress., • Carry out occasional visits to international clients and suppliers. Requirements • High level of English, both spoken and written., • Proven experience in international sales, ideally within the consumables sector., • Strong negotiation, communication and organizational skills., • Ability to work independently and proactively in multicultural environments., • Knowledge of other languages (French, German, Italian, etc.)., • Experience managing international accounts within a corporate group., • Analytical mindset with strong attention to detail and results orientation. What We Offer • The opportunity to work on an international project within a growing organization., • Professional development in a collaborative and multicultural environment., • Autonomy to manage your projects and contribute new ideas., • A dynamic, supportive and result-driven team culture.

At its locations around the world, Siegfried offers employees exciting career opportunities in international settings. We cultivate multidisciplinary cooperation and encourage our staff to actively shape and influence their careers. This approach, coupled with our dynamic working environment, make Siegfried an attractive employer. Your role: • Comprehensive Product Management: Oversee the entire commercial lifecycle of the product, from its transfer by development to the present date, acting as the Single Point of Contact (SPOC)., • Risk Analysis and Quality Control: Create, update, and monitor the product-specific Quality Risk Analysis (QRA) and ensure compliance with quality standards., • Data Monitoring and Analysis: Evaluate critical and key variables through statistical analysis, track data trends, and review the Annual Product Quality Review (APQR) to make informed decisions regarding control status., • Inspection Readiness: Ensure all aspects related to the product process are prepared for audits and regulatory inspections., • Performance Monitoring and Improvement: Identify trends, detect issues, and lead the implementation of corrective and preventive actions (CAPAs) to enhance products., • Deviation Management and Improvement Projects: Investigate process deviations, lead optimization projects, and engage cross-functional teams in improvement initiatives., • In-Process Controls (IPC) Monitoring: Ensure the tracking of critical parameters in laboratories and guarantee that data is visible and communicated at the plant level., • Technical Change Assessment: Analyze the impact of process modifications, determine their feasibility, and manage the quotations associated with these changes., • Process and Product Validation: Ensure continuous validation status, alignment with the APQR, and implementation of control strategies based on Critical Quality Attributes (CQA), Critical Process Parameters (CPP), and Critical Material Attributes (CMA)., • Product Launch and Transfer: Facilitate product transfers by ensuring technical documentation and providing necessary support to the receiving plant., • Manufacturing Optimization and Excellence: Lead improvement projects to enhance the robustness and sustainability of pharmaceutical processes in collaboration with Operational Excellence (OPEX). Your profile: • University degree in a scientific field or related, or a higher vocational training degree in a scientific field with previous experience in a similar position., • High level of English., • Experience in a similar technical position and in the pharmaceutical sector., • Knowledge of data management and application of statistical techniques. Working at Siegfried Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs. In the Midst of People’s Lives – Across the Globe The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products.

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 5 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!

Desde ManpowerGroup Talent Solutions estamos buscando un.Experto en implementaciones desde cero de LIMS.Dentro del departamento de IT Quality and Compliance, tus funciones principales serán:.Implementar un sistema LIMS desde cero para gestionar integralmente los laboratorios de Control de Calidad e

Account Manager - Medical Device International Role | Medical Devices | Hybrid Work | Fast-Growing Team ___ is an innovative technological company dedicated to the development and commercialization of medical devices in the fields of neuro, spinal and cardiac surgery. Offices based in Cerdanyola del Valles (Barcelona).Their mission is to provide worldwide surgeon with innovative solutions. As Account Manager, you will be responsible for driving business growth in assigned territories, managing distributor relationships, and supporting the adoption of their innovative products in hospitals across the globe. You will work closely with surgeons and distributors, combining sales drive with hands-on product application support. This is an exciting opportunity to join a small but highly dynamic team and where your work will have direct impact on our growth. Your Role & Responsibilities: • Build and maintain strong relationships with distributors, creating added value through business growth., • Manage the full sales cycle in your assigned territories: from identifying opportunities and negotiating contracts to closing deals., • Support distributors with joint hospital visits, sales model reviews, product trainings, and assistance during surgeries., • Travel occasionally to meet clients, attend congresses, and represent NEOS Surgery internationally., • Identify new sales channels, expand distributor databases, and support overall business development., • Stay ahead of industry trends: analyse competitors, benchmark the market, and share insights with the team., • Collaborate closely with Marketing, Clinical, R&D, Quality, and Regulatory departments., • Master our product portfolio and work hand-in-hand with our product specialist to resolve customer queries., • Co-create marketing tools and solutions tailored to specific customer needs. What We’re Looking For: • Degree in Life/Health Sciences, Economics, or Business Administration., • 2–4 years of professional experience, ideally in the medical device sector., • Strong ambition to develop a career in business development and sales., • Previous commercial/sales experience is a plus, but not essential., • Fluent English, • Willingness to travel internationally Why Join NEOS Surgery? • Be part of a young, dynamic, and ambitious team where entrepreneurship and initiative are valued., • Work in the fast-growing medical devices sector with an international presence in 20+ countries., • Experience a flexible and hybrid work environment, designed to empower high performance and personal growth., • Join a company on the rise, where you will have real impact and grow alongside the business.

Sales Area Manager - Medical Device International Role | Medical Devices | Hybrid Work | Fast-Growing Team NEOS Surgery is an innovative technological company dedicated to the development and commercialization of medical devices in the fields of neuro, spinal and cardiac surgery. Offices based in Cerdanyola del Valles (Barcelona).Their mission is to provide worldwide surgeon with innovative solutions. As Sales Area Manager, you will be responsible for driving business growth in assigned territories, managing distributor relationships, and supporting the adoption of their innovative products in hospitals across the globe. You will work closely with surgeons and distributors, combining sales drive with hands-on product application support. This is an exciting opportunity to join a small but highly dynamic team and where your work will have direct impact on our growth. Your Role & Responsibilities: • Build and maintain strong relationships with distributors, creating added value through business growth., • Manage the full sales cycle in your assigned territories: from identifying opportunities and negotiating contracts to closing deals., • Support distributors with joint hospital visits, sales model reviews, product trainings, and assistance during surgeries., • Travel occasionally to meet clients, attend congresses, and represent NEOS Surgery internationally., • Identify new sales channels, expand distributor databases, and support overall business development., • Stay ahead of industry trends: analyse competitors, benchmark the market, and share insights with the team., • Collaborate closely with Marketing, Clinical, R&D, Quality, and Regulatory departments., • Master our product portfolio and work hand-in-hand with our product specialist to resolve customer queries., • Degree in Life/Health Sciences, Economics, or Business Administration., • 2–4 years of professional experience, ideally in the medical device sector., • Strong ambition to develop a career in business development and sales., • Previous commercial/sales experience is a plus, but not essential., • Fluent English, • Be part of a young, dynamic, and ambitious team where entrepreneurship and initiative are valued., • Work in the fast-growing medical devices sector with an international presence in 20+ countries., • Experience a flexible and hybrid work environment, designed to empower high performance and personal growth., • Join a company on the rise, where you will have real impact and grow alongside the business.

At its locations around the world, Siegfried offers employees exciting career opportunities in international settings. We cultivate multidisciplinary cooperation and encourage our staff to actively shape and influence their careers. This approach, coupled with our dynamic working environment, make Siegfried an attractive employer. Your role: • Comprehensive Product Management: Oversee the entire commercial lifecycle of the product, from its transfer by development to the present date, acting as the Single Point of Contact (SPOC)., • Risk Analysis and Quality Control: Create, update, and monitor the product-specific Quality Risk Analysis (QRA) and ensure compliance with quality standards., • Data Monitoring and Analysis: Evaluate critical and key variables through statistical analysis, track data trends, and review the Annual Product Quality Review (APQR) to make informed decisions regarding control status., • Inspection Readiness: Ensure all aspects related to the product process are prepared for audits and regulatory inspections., • Performance Monitoring and Improvement: Identify trends, detect issues, and lead the implementation of corrective and preventive actions (CAPAs) to enhance products., • Deviation Management and Improvement Projects: Investigate process deviations, lead optimization projects, and engage cross-functional teams in improvement initiatives., • In-Process Controls (IPC) Monitoring: Ensure the tracking of critical parameters in laboratories and guarantee that data is visible and communicated at the plant level., • Technical Change Assessment: Analyze the impact of process modifications, determine their feasibility, and manage the quotations associated with these changes., • Process and Product Validation: Ensure continuous validation status, alignment with the APQR, and implementation of control strategies based on Critical Quality Attributes (CQA), Critical Process Parameters (CPP), and Critical Material Attributes (CMA)., • Product Launch and Transfer: Facilitate product transfers by ensuring technical documentation and providing necessary support to the receiving plant., • University degree in a scientific field or related, or a higher vocational training degree in a scientific field with previous experience in a similar position., • High level of English., • Experience in a similar technical position and in the pharmaceutical sector. Benefits: • Annual Bonus: 7.5%, • Two days of home office per week, • Free parking, • Good public transport available to reach the site, • Subsidized canteen on-site or restaurant ticket: to use when eating out or working from home, • Medical, life, and accident insurance In the Midst of People’s Lives – Across the Globe The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products.

Develop practicable, sustainable actions at shopfloor, compliant to Quality standard requirements, alignment with Production, Engineering .CP moderation, outline risk reduct.Participate in ADP/MOC projects and support processes requiring Quality involvement .Root-cause-analysis, corrective action, p

Continuous improvement mindset: Commitment to maintaining and enhancing quality standards at the plant. Previous experience in a Quality department, preferably within the automotive sector. Develop practicable, sustainable actions at shopfloor, compliant to Quality standard requirements, alignment w

Develop practicable, sustainable actions at shopfloor, compliant to Quality standard requirements, alignment with Production, Engineering .CP moderation, outline risk reduct.Participate in ADP/MOC projects and support processes requiring Quality involvement .Root-cause-analysis, corrective action, p

Our final objective is to improve people's quality of life through sustainable and environmentally friendly infrastructures.Specifically, we want to incorporate knowledge into the development of port infrastructure projects (experts in ports, water, the environment, and special structures).Thanks to

Modify and update manufacturing instructions and other production-related documents.Prepare quotations for new parts following the established procedure.Prepare documentation and follow up on online tests.Prepare and manage test shipments.Conduct quality “GEMBA” walks to ensure correct operation

Modify and update manufacturing instructions and other production-related documents.Prepare quotations for new parts following the established procedure.Prepare documentation and follow up on online tests.Prepare and manage test shipments.Conduct quality “GEMBA” walks to ensure correct operation

Modify and update manufacturing instructions and other production-related documents.Prepare quotations for new parts following the established procedure.Prepare documentation and follow up on online tests.Prepare and manage test shipments.Conduct quality “GEMBA” walks to ensure correct operation

Apply lean manufacturing tools to achive targets fixed by the management .Monitors the quality of output to identify or discard re-manufacture faulty products .Maintains accurate daily production records so that manufacturing performance can be analyzed .Design, implement and maintain systems to col

Apply lean manufacturing tools to achive targets fixed by the management .Monitors the quality of output to identify or discard re-manufacture faulty products .Maintains accurate daily production records so that manufacturing performance can be analyzed .Design, implement and maintain systems to col

Apply lean manufacturing tools to achive targets fixed by the management .Monitors the quality of output to identify or discard re-manufacture faulty products .Maintains accurate daily production records so that manufacturing performance can be analyzed .Design, implement and maintain systems to col

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

Empresa cárnica en Montornés precisa incorporar a un mozo/peon para mover, paletizar y almacenar mercancía congelada.

Desde Temporal Quality tenemos una nueva oportunidad laboral para una importante empresa del. Experiencia de al menos 1 año gestionando pedidos, resolviendo incidencias y haciendo soporte al departamento comercial. ETT de 6 meses con pase a indefinido posterior.

Temporal Quality selecciona para una importante empresa de Cerdanyola del sector logístico:.LA OPERATIVA SE INICIA 20 DE OCTUBRE.Buscamos personal polivalente y comprometido para realizar las siguientes actividades:.Manipulación, revisión y organización de libros de forma automatizada y manual.S

Disponibilidad para trabajar de Lunes a Viernes en turno de mañana/tarde. Empresa especializada en el sector del material técnico y la impresión 3D, situada en Polinya, precisa incorporar personal como chofer + carretillero. Suministro de materiales a la línea de producción.

Empresa ubicada en Barberá del Valles del sector alimentación, precisa operario de mantenimiento para sus instalaciones.Experiencia minima en electricidad industrial, fontanería y mecánica.Funciones: dar apoyo a nuevos proyectos que hay en el área de mantenimiento (averías, reparaciones, mante

Funciones: Entradas, salidas, preparación de pedidos, picking con PDA, ubicación de material, etiquetado, encajado, manipulación en almacén entre otras tareas derivadas del puesto. Empresa logística ubicada en Sabadell Sud precisa incorporar mozo/a manipulador/a para campaña textil y libros:.

Desde Temporal Quality tenemos una nueva oportunidad laboral para una importante empresa del sector de la automoción ubicada en Palau- solitá i plegamans.El perfil solicitado es para la posición de.Se busca formar talento interesado y motivado en el mundo comercial.Sobre todo buscamos a alguien c

Empresa logística ubicada en Sabadell Sud precisa incorporar mozo/a manipulador/a.

Desde Temporal Quality tenemos una nueva oportunidad laboral para una importante empresa del.Las condiciones que se ofrecen son:.ETT con pase a indefinido posterior.K € b/a según experiencia aportada.Si crees que puedes encajar y estás motivado/a a dar un impulso a tu carrera con este reto, ¡po

Empresa logística ubicada en Sabadell Sud precisa incorporar mozo/a manipulador/a.Funciones: Clasificación de mercancía, recuperado de libros, cambio de caja de producto, preparación de pedidos, picking con PDA, ubicación de material, etiquetado, encajado, manipulación en almacén entre otras

Experiencia demostrable mínimo de 6 meses desarrollando las funciones descritas. Te apasiona el mundo de la automoción y tienes experiencia gestionando equipos en linea de montaje y manipulación de piezas?. Mantenimiento básico de equipos en la línea de producción (puesta en marcha, parametriz

Empresa logística ubicada en Sabadell Sud precisa incorporar mozo/a manipulador/a con carretilla, transpaleta electrica.

Empresa situada en Polinyà y especializada en corete de madera, cartón y metacrilato, precisa incorporar mozos/as de almacén con carné de carretilla. Carnet de conducir y vehiculo propio.

Estamos buscando un/a Senior Quality Technician.

Create and maintain supplier quality evaluation and control systems to ensure consistent quality standards. This role involves developing, implementing, and maintaining quality assurance protocols to ensure supplier compliance and product quality. Revlon’s quality standards and specifications.

As a Quality Engineer in the automotive sector, you will be responsible for developing a plan and implementing a systematic approach to ensure that all defined automotive standards, practices, procedures and methods are adhered to by management. Receives and channels complaints regarding customer qu

Working on leading-edge AWS-hosted applications, the QA Engineer will develop and execute both automated and manual testing scenarios to ensure the delivery of high-quality software products.

Quieres dar tus primeros pasos en el mundo laboral y desarrollar tu vocación? ¡¡Ha llegado tu momento!! En.Lidera tu camino y únete a nuestro Talent Program Pathfinder! Una experiencia en la que TÚ serás protagonista.Pero no te preocupes, no lo harás en solitario.Tendrás guías que te acompa

Servicios de Executive Search, RPO y Soluciones de Talento.Nuestra misión es impulsar el crecimiento y la realización tanto de personas como de organizaciones.Facilitamos a las personas la búsqueda de oportunidades inspiradoras y ayudamos a las organizaciones a identificar profesionales que las l

Combinamos innovación, precisión y compromiso con la calidad para ofrecer soluciones ligeras, resistentes y de alto rendimiento a clientes internacionales líderes en su sector.Asegurar que los productos cumplen los requisitos del cliente y de los procesos internos, desde la recepción de material