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Te gustaría supervisar una sección clave dentro de una empresa industrial referente en maquinaria industrial?Nuestro cliente, empresa fabricante de maquinaria precisa incorporar un/a:SUPERVISOR DE MECANIZADOSð Granollers (Barcelona)QUÉ OFRECEMOS:Contrato indefinido en empresa industrial consolid

Job ID: jefe-de-turnos-74c81ed1-14b9-498a-8b01-bfdb599d549bTeléfono: 955292054Desde IMAN Global Consulting, Consultoría de Selección de perfiles Technical, Middle, C-Suite, buscamos a un candidato/a Jefe/a de turnos, para trabajar en una empresa del sector metal, ubicada en Granollers, Barcelona:

Back to search results R&D Product Designer Location: Pamplona, ES Blackburn, GB Poznan (FBS), PL Bremervorde, DE Campo Real, ES Lubien, PL Cardedeu Barcelona, ES Sant Cugat, ES Besancon, FR Rushden, GB Bouxwiller, FR La Genete, FR Oakham, GB Department: R&D/Innovation Management Full-time or Part-time: Full-Time Job Type: Employee Shift: Remote Accelerate the possible by joining a winning Amcor team that’s transforming the packaging industry and improving lives around the world. At Amcor, we unpack possibility through our innovative and responsible packaging to provide solutions that benefit our customers, our people and our planet. More than 10,000 consumers worldwide encounter our products every second and rely on us for safe access to food, medicine and other goods. We value their trust by making safety our guiding principle. It's our core value and integral to how we do business. Beyond this core principle, our shared values and behaviors unite us as we work together to elevate customers, shape lives and protect the future. We champion our customers and help them succeed. We play to win - adapting quickly in an everchanging world - and make smart choices to safeguard our business, our communities and the people we serve for generations to come. And we invest in our world class team, empowering our colleagues to unpack their potential, because we believe when our people grow, so does our business. To learn more about playing for Team Amcor, visit www.amcor.com I LinkedIn I Glassdoor I Facebook I YouTube Development or Expert Center Manager or Advance Innovation Manager The R&D Product Designer role is responsible for conceptualizing, designing, and developing new products that align with our company’s strategic goals. This position requires a blend of creative design skills, project management skills and technical expertise. • Sustainability: Implement and scale sustainable business practices across operations and value chain, focusing on reducing environmental impact while maximizing circularity and enhancing value creation., • Product Innovation: Creating new and improved packaging designs that meet the evolving needs of customers across various industries., • Cost Innovation: Value creation by reducing the costs associated with producing or delivering a product or service, while maintaining or improving its quality and performance., • Generate innovative product concepts based on market research, customer feedback, and emerging trends., • Be project manager and ensure that the projects are updated and follow our stage gate model., • Manage multiple projects simultaneously, ensuring timely delivery and adherence to budget constraints., • Create detailed design specifications, sketches, and prototypes using CAD software and other design tools., • Work closely with cross-functional teams including engineering, marketing, and manufacturing to ensure design feasibility and alignment with business objectives., • Conduct product testing and iterate designs based on feedback and performance data., • Stay updated with the latest industry trends, technologies, and materials to continuously bring fresh ideas to the table to be presented to the R&D Expert Centers team on a quarterly basis., • Maintain comprehensive documentation of design processes, specifications, and project progress., • Tracks the number of innovative product ideas generated within a specific period., • Measures the time taken to move from concept to prototype, indicating efficiency in the design process., • Measure the percentage of prototypes that successfully pass testing phases and move to the next stage of development., • Evaluates the financial return generated from new products relative to the investment made in their development., • Bachelor’s or Master’s degree in Industrial Design, Product Design, Engineering, or a related field., • Minimum of 5 years of experience in product design and development, preferably in an R&D environment., • Proficiency in CAD software (e.g., SolidWorks, KeyShot, etc)., • Strong understanding of materials, manufacturing processes, and engineering principles., • Excellent problem-solving skills and attention to detail., • Ability to think creatively and innovatively., • Strong communication and teamwork skills., • Project management experience is a plus. Amcor is the global leader in developing and producing responsible consumer packaging and dispensing solutions across a variety of materials for nutrition, health, beauty and wellness categories. Our global product innovation and sustainability expertise enables us to solve packaging challenges around the world every day, producing a range of flexible packaging, rigid packaging, cartons and closures that are more sustainable, functional and appealing for our customers and their consumers. We are guided by our purpose of elevating customers, shaping lives and protecting the future. Supported by a commitment to safety, over 75,000 people generate $23 billion in annualized sales from operations that span over 400 locations in more than 40 countries. Amcor is committed to providing a secure and reliable experience for all job seekers. If you are looking to join Amcor, please read this page to help you avoid recruitment scams. NYSE: AMCR; ASX: AMC www.amcor.com | LinkedIn | YouTube #J-18808-Ljbffr

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. Position part of the procurement team focused in improving and re-evaluating the procurement activities, optimizing the organization's supply base and increasing its overall value proposition. Focused on the total cost of ownership, this position also considers product quality, customer needs, organizational goals and market conditions as an essential part of the procurement process. Actions are driven by a rigorous and collaborative approach, based on fact analysis and market intelligence, following the Strategic Sourcing Framework. Key Accountabilities Ensure the availability of raw material, both; short and long term, through regular monitorization of critical raw materials and a continuous analysis of risks to define risk mitigation actions. Regular reporting and analysis of the main purchasing KPIs, such as • OTIF, • Expired material, • Obsolescence, • Monthly stock report Main responsible for the price negotiation and the management of materials savings initiatives in line with profit plan and overall business objectives. Negotiation of supply agreements as needed to support the critical business needs: • Monitorization and renewal of existing Supply and Quality Agreements, • Ensures Supply and Quality Agreements are positioned appropriately before business is initiated with new vendors Improve the value-to-price relationship with suppliers following Strategic Sourcing Framework • Quarterly communication of raw material forecast, • Follow up calls with all the vendors, • Annual visit plan with key vendors, • Attendance to main exhibitions Supports Supplier Quality department to accomplish the goals defined in supplier quality system • Annual risk analysis of raw materials and definition of key vendors list, • Analysis of vendors performance Ensure the maximum quality of the purchased products Follow up of technical problems with Supplier Quality, Technical Support, R&Dor Manufacturing departments Contribute to keep updated the material and supplier database Strategic activities: • Development and implementation of the Strategic Sourcing strategy, • Develop key performance measures for chosen suppliers and negotiate on multiple variables to award longer-term strategic contracts that result in significant cost reduction and improved service levels, • Monitor current category market conditions, technology roadmaps and identify supply/demand challenges & opportunities., • Identification of new suppliers in collaboration with R&D during the development of new products, • Identification of potential risk and definition of mitigation action plans, • Involvement in the total cost analysis for new product developments Internal Networking To be determined based on department needs, to include interactions such as: • Supplier Quality: Control change notification management and vendor's complaints support, • Manufacturing: Support in solving technical issues related to raw material or packaging performance, • R&D: Support in the development of new products and identifying suppliers for new assays, • Supply Chain Department; Including warehouse and planning, • Sales and Marketing: Benchmarking of vendors, • Quality Control Minimum Knowledge & Experience required for the position Education: • Required:Bachelor'sdegree(Diplomatura)inthebiologicalorrelatedsciences.Degreemaybesubstitutedbyrelevantskillsandworkexperience, • Valuable:Anyadditionaldegreehigherthantherequired Experience: Minknowledge • Software:FluencyinOfficeTools(Excel&Word),ValuableadvancedknowledgeinSAP, • Language:FluencyinSpanishorCatalan.AdvancedknowledgeofEnglish(reading,writingandspeaking) AdditionalSkills/Knowledge: • Software:FluencyinOfficeTools(Excel&Word),ValuableAdvancedknowledgeinSAP, • Language:FluencyinSpanishorCatalan.MediumknowledgeofEnglishreading,writingandspeaking) Skills & Capabilities The ideal candidate for this position will exhibit the following skills and competencies: • Management of decisions under pressure., • Methodical and well-organized person., • Teamwork., • Ability to express information clearly and concisely to the staff, ensuring their understanding., • Ability to apply a systematic approach and constant control, follow-up and verification of the results., • Ability to collaborate, participate and coordinate actively with working groups., • Good reporting and analysis capabilities., • Reflects values of Werfen in the quality of work and working relationship. Travel Requirements 5% of the time Werfen appreciates and values diversity. We are an Equal Opportunity/Affirmative Action Employer M/F/D/V. #J-18808-Ljbffr

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.We operate directly in 30 countries, and in more than 100 terri

Werfen, a global diagnostics leader, seeks a Regulatory Affairs professional to provide regulatory support for our manufactured and customer products.You will prepare submissions and implement new regulatory requirements.Based in Barcelona, you will coordinate with R&D, QA, and Regulatory agencies t

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. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters are in Barcelona, Spain and our Technology Centers are located in the United States and Europe. Worldwide sales exceeded €2.2 billion in 2024, and our workforce is more than 7,000 strong. The Quality Systems (QS) Engineer is responsible for maintaining the core Quality Management System (QMS) processes, including Document Control, Change Control, Internal Audit and Training Management, and ensure the company is compliant with all applicable regulations and standards. The QS Engineer operates with a high degree of autonomy in the planning, coordination and execution of audits, and, upon qualification through the internal auditor qualification program, is authorized to conduct internal audits independently. The role serves also as a subject matter experts (SME) for the QS processes, providing technical guidance and support across the organization. In addition, the QS Engineer actively contributes to the continual improvement of the QRA function and supports the effective management of Non-conformance, Corrective and Preventive Actions (CAPA), and other quality system improvement initiatives. • Organize and coordinate internal and external audits, including planning, execution and follow-up activities., • Conduct internal audits upon successful completion of the Internal Auditor Qualification Program., • Lead backroom activities during external audits and host the frontroom activities during internal audits., • Develop the annual Quality Training Program based on identified organization needs, support its deployment, and monitor its effective execution., • Collect, analyse and communicate training feedback to trainers to support the continous improvement of training content and delivery method., • Oversee the preparation, implementation and completion of Annual Training Plans., • Design and develop training materials, and provide guidance and support to other departments in training-related activities., • Deliver Quality and GMP-related training sessions across the organization., • Maintain the Documentation Management System., • Manage documents of external origin. Participate in the impact assessments, action plan definition and follow up of the changes needed., • Coordinate Management Review activities and maintain the associated documentation., • Prepare general internal communications within the Quality and Regulatory Affaris (QRA) area., • Maintain the Change Management System, ensuring effective coordination, tracking and timely implementation of changes and associated actions., • Perform quality assessment of change requests, as required., • Monitor, analyse and report the Key Performance Indicators (KPIs) related to QS-owned processes., • Own Non Conformities, Change Controls and CAPA directly involving QS-owned processes., • Manage Non Conformities, Change Controls and CAPA related to cross-functional Quality Management System processes., • Monitor the progress and timely closure of audit-related Non conformances and associated CAPA., • Participate in the design, implementation and continuous improvement of core Quality System processes., • Prepare and maintain Quality Management System documentation required to support international registrations, in accordance with the registration timelines., • Respond to customer quality questionnaries., • Manage projects autonomously and actively contribute to the continual improvement of the department., • Serve as a subject matter expert (SME) of QS-owned processes during audits and inspections, and providing guidance and support across the organization. This position involves frequent interaction with all areas of the company and includes delivering training to employees across different functions. • Required: Bachelor’s degree (Grado) in Chemistry, Biotechnology or other Sciences, complete with competency in chemical, biological, or health-related work experience., • Degree may be substituted by relevant skills and work experience., • Valuable: Any additional academic qualification beyond those required in the previous section, including a Master’s degree in Quality Management., • Minimum of 3 years in a similar position., • Software: Good knowledge of Microsoft Office and Adobe applications. Basic SAP knowledge is desirable, together with a proven ability to adapt to new technologies. Experience in digitalizing and optimizing processes will be considered an asset., • Language: fluent in Spanish and/or Catalan, with advanced English communication skills (both written and spoken)., • Standards: Extensive knowledge of regulatory requirements applicable to medical devices and/or in vitro diagnostic medical devices, as well as Quality Management Systems. Knowledge of additional regulations and standards will be considered an asset. Management reserves the right to substitute relevant professional experience for academic qualifications and/or to make exceptions to the required years of experience., • Management of decisions under pressure., • Methodical and well-organized person., • Ability to apply a systematic approach and constant control, follow-up and verification of the results., • Time-management skills., • Teamwork., • Ability to collaborate, participate and coordinate actively with working groups., • Excellent communication skills, with the ability to present information clearly and concisely while ensuring audience understanding., • Reflects values of Werfen in the quality of work and working relationships. Not required. #J-18808-Ljbffr

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. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters are in Barcelona, Spain and our Technology Centers are located in the United States and Europe. Worldwide sales exceeded €2.2 billion in 2024, and our workforce is more than 7,000 strong. Solutions QA Leader focuses on organizational aspects of quality management, aiming to improve the end-to-end product development life cycle, from requirements analysis to launch and maintenance, including providing inputs and active contributions to the definition and maintenance of the Quality Management System (QMS). Working closely with the Solutions Leaders to ensure to deliver software releases with an ever-increasing level of quality. When applicable, QA Customer Liaison facilitating effective communication and understanding of QA processes, methodologies, and outcomes. • Cooperating with the Director of Quality & Regulatory Affairs - Digital Solutions to co-ordinate quality assurance activities for all SW development products assigned., • Responsible for ingraining quality as a core discipline into every aspect of the SW development teams (Squads) organizations., • Ensure that SW Development teams (Squads) are informed with the perspective of the QA processes and/or customer requirements enabling the delivery of a product or service to an agreed level of quality., • Oversee SW project documents subject to QA approval ensuring the establishment and adherence to the appropriate QMS and customer processes and procedures, including but not limited to requirements management, configuration control, secure design, risk analysis, verification and validation, traceability, etc., • Support Change Management Board (CRB) process as needed., • Advance metrics and the setting of goals that provide visibility and understanding of development effectiveness from a quality perspective., • Drive Promote continuous improvement initiatives to enhance product quality, operational efficiency, and customer satisfaction., • Collaborate in the QS software development life cycle procedures definition and maintenance. Provides input in the implementation of the process., • Point of contact for the different business unit's / client related with Quality agreements, • Take an active role in the training and dissemination of knowledge regarding quality system procedures., • Pursuing a unified approach to quality process implementation throughout the software development lifecycle across all solutions within a Factory., • Participate in software products audits and assessments as needed. The main relationships within the Werfen Group are: • Factory Lead and Solution Leaders, • Solutions QA Leaders from other factories, • SW Development Teams (Squads) and Chapter Leads, • QARA Manager and QARA Specialist, • Customer, • Validation Lead, • Application Lifecycle manager (ALM), • This position may also require cooperating with other companies inside Werfen., • Education: Engineer, computer Science or other Technical degree, or equivalent work experience., • Experience:, • A minimum of 5 years of experience in a QA related role., • Knowledge in SW Development methodologies preferably within the Healthcare sector., • Experience in the creation or revision of comprehensive software products documentation., • Additional Skills/Knowledge:, • Knowledge about applicable standards and regulations related with SW development for Health and/or Medical Device. (ISO 13485, ISO 14971, IEC 62304, IEC 82304, ISO 62366, cybersecurity), • Familiar with medical device regulations (MDR/IVDR, FDA, etc) This position has a combination of technical and leadership experience in QA area being able to collaborate seamlessly with cross-functional teams for ensuring product quality and customer and regulatory compliance. The role requires demonstrates adaptability to evolving technologies, strong communication skills, and a commitment to fostering a quality-focused culture within the organization. Besides it is needed to have: • Strong interpersonal skills with a proven ability to collaborate across teams and communicate effectively with stakeholders., • Flexibility and adaptability to a fast-changing environment/methodology, • Self-organized and self-monitor to be able to report the effort dedicated to each individual tasks inside all the different responsibilities., • Good level of Technical and Conversational English, • Commitment to continuous improvement, with a track record of implementing initiatives to enhance overall quality processes. 5% of time #J-18808-Ljbffr

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. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters are in Barcelona, Spain and our Technology Centers are located in the United States and Europe. Worldwide sales exceeded €2.2 billion in 2024, and our workforce is more than 7,000 strong. The Maintenance Manager is responsible for ensuring the safe, reliable and compliant operation of industrial maintenance and hard facility services in a regulated manufacturing environment. The role oversees corrective and preventive maintenance, calibration activities, utilities, infrastructure, technical documentation, contractor performance and budget control. It requires strong technical knowledge, leadership capability, cross-functional collaboration and a continuous focus on safety, compliance, service quality and business continuity. Industrial Maintenance: Including corrective maintenance, preventive maintenance and calibration management, ensuring equipment reliability, compliance and operational continuity. Hard Facility Services: Including utilities, infrastructure and building-related technical services, through a fully outsourced model, ensuring effective contractor performance and alignment with site needs. Budget Control: Define, monitor and control the maintenance expenditures and investments, optimizing financial, technical and human resources according to business priorities. Technical Documentation Management: Manage technical and legal documentation, technical drawings and electrical schematics related to facilities, utilities and equipment, ensuring accuracy, availability, version control and readiness for audits, inspections and maintenance activities. Operations and Manufacturing: Alignment of maintenance priorities and production continuity. Engineering, Automation and Projects: Coordination of installations, upgrades and infrastructure improvements. Quality, Regulatory Affairs and Compliance: Support for documentation, deviations, audits and GMP/ISO requirements. EHS, Security and Facility Management: Oversight of safety, permits and infrastructure risks. R&D, Laboratories and Technical Services: Support for laboratory, cleanroom and equipment requirements. Suppliers, Service Providers and Subcontractors: Planning, supervision and performance monitoring. People Function and Leadership: Coordination of workforce planning, team development and performance management. Education: Bachelor's degree in Engineering, Industrial Engineering, Maintenance, Facilities Management or a related technical field. Additional training in facilities, utilities, project management, safety or regulated environments is valued. Experience: At least 5 years in maintenance, hard facilities, utilities or engineering management, preferably in regulated manufacturing, diagnostics, medical devices, pharmaceutical, biotechnology or laboratory environments. People Management: Experience leading technical teams, setting priorities and developing team capabilities. Technical Knowledge: Knowledge of preventive and corrective maintenance, HVAC, cleanrooms, purified water, electrical, pneumatic, mechanical, instrumentation and laboratory facility systems. Project and Contractor Management: Experience managing renovations, installations, commissioning support, subcontracted work, budgets and technical documentation. Systems and Tools: Proficiency in Microsoft Office and maintenance management systems; SAP knowledge required or strongly preferred. Languages: Fluency in Spanish or Catalan, with advanced English for technical documentation and communication. Compliance: Knowledge of safety requirements, audit readiness and GMP/ISO 13485-oriented practices. Sound decision‑making under pressure, balancing safety, compliance, cost and business continuity. Structured and disciplined approach to planning, execution and follow‑up. Ability to lead technical teams, develop capabilities and foster accountability and collaboration. Clear and effective communication with users, managers, suppliers and cross‑functional stakeholders. Strong prioritization and time management in demanding environments. Analytical approach to root cause analysis, risk assessment and sustainable improvement. Service‑oriented mindset focused on internal customer needs. Effective collaboration with multidisciplinary teams and external partners. Strong commitment to safety, compliance, documentation discipline and Werfen values. Occasional travel may be required, typically less than 5% of working time. #J-18808-Ljbffr

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. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters are in Barcelona, Spain and our Technology Centers are located in the United States and Europe. Worldwide sales exceeded €2.2 billion in 2024, and our workforce is more than 7,000 strong. Solutions QA Leader focuses on organizational aspects of quality management, aiming to improve the end-to-end product development life cycle, from requirements analysis to launch and maintenance, including providing inputs and active contributions to the definition and maintenance of the Quality Management System (QMS). Working closely with the Solutions Leaders to ensure to deliver software releases with an ever-increasing level of quality. When applicable, QA Customer Liaison facilitating effective communication and understanding of QA processes, methodologies, and outcomes. • Cooperating with the Director of Quality & Regulatory Affairs - Digital Solutions to co-ordinate quality assurance activities for all SW development products assigned., • Responsible for ingraining quality as a core discipline into every aspect of the SW development teams (Squads) organizations., • Ensure that SW Development teams (Squads) are informed with the perspective of the QA processes and/or customer requirements enabling the delivery of a product or service to an agreed level of quality., • Oversee SW project documents subject to QA approval ensuring the establishment and adherence to the appropriate QMS and customer processes and procedures, including but not limited to requirements management, configuration control, secure design, risk analysis, verification and validation, traceability, etc., • Support Change Management Board (CRB) process as needed., • Advance metrics and the setting of goals that provide visibility and understanding of development effectiveness from a quality perspective., • Drive Promote continuous improvement initiatives to enhance product quality, operational efficiency, and customer satisfaction., • Collaborate in the QS software development life cycle procedures definition and maintenance. Provides input in the implementation of the process., • Point of contact for the different business unit's / client related with Quality agreements, • Take an active role in the training and dissemination of knowledge regarding quality system procedures., • Pursuing a unified approach to quality process implementation throughout the software development lifecycle across all solutions within a Factory., • Participate in software products audits and assessments as needed. The main relationships within the Werfen Group are: • Factory Lead and Solution Leaders, • Solutions QA Leaders from other factories, • SW Development Teams (Squads) and Chapter Leads, • QARA Manager and QARA Specialist, • Application Lifecycle manager (ALM), • This position may also require cooperating with other companies inside Werfen., • Education: Engineer, computer Science or other Technical degree, or equivalent work experience., • A minimum of 5 years of experience in a QA related role., • Knowledge in SW Development methodologies preferably within the Healthcare sector., • Experience in the creation or revision of comprehensive software products documentation., • Additional Skills/Knowledge:, • Knowledge about applicable standards and regulations related with SW development for Health and/or Medical Device. (ISO 13485, ISO 14971, IEC 62304, IEC 82304, ISO 62366, cybersecurity), • Familiar with medical device regulations (MDR/IVDR, FDA, etc) This position has a combination of technical and leadership experience in QA area being able to collaborate seamlessly with cross-functional teams for ensuring product quality and customer and regulatory compliance. The role requires demonstrates adaptability to evolving technologies, strong communication skills, and a commitment to fostering a quality-focused culture within the organization. Besides it is needed to have: • Strong interpersonal skills with a proven ability to collaborate across teams and communicate effectively with stakeholders., • Flexibility and adaptability to a fast-changing environment/methodology, • Self-organized and self-monitor to be able to report the effort dedicated to each individual tasks inside all the different responsibilities., • Good level of Technical and Conversational English, • Commitment to continuous improvement, with a track record of implementing initiatives to enhance overall quality processes. #J-18808-Ljbffr

Werfen seeks a QS Engineer to maintain the core QMS, manage audits, and drive continual improvement across the organization. You will act as an SME for QS processes and support CAPA and change control activities. The role requires a bachelor’s in a science field, several years in quality, and fluency in English with Spanish or Catalan skills. SAP knowledge and regulatory awareness are valued in this on-site Barcelona area position. #J-18808-Ljbffr

We're Hiring | Regulatory Affairs Specialist – Barcelona / ValenciaEMEA Pharma Business UnitAt Brenntag, the global market leader in chemicals and ingredients distribution, we're looking for a Regulatory Affairs Specialist to join our team in Barcelona o Valencia.If you're passionate about regulatory compliance, enjoy working in an international environment, and want to make an impact by supporting regulatory excellence across the business, we'd love to hear from you.Role OverviewAs a key member of the Pharma team, you will support the EMEA division on all regulatory, quality, compliance, legal, and product stewardship topics related to the supply of a large portfolio of raw materials into the pharmaceutical industry. ¿Es este su próximo empleo? Descúbralo leyendo la descripción completa a continuación y no dude en enviar su candidatura. Your primary responsibility is to provide accurate, timely, and audit‑ready documentation to pharmaceutical customers and to support regulatory deliverables for bespoke product projects.The role is primarily office‑based, with occasional travel required for supplier meetings, customer visits, audits, or internal workshops.You will collaborate closely with commercial, supply chain, QHSE, and supplier partners to ensure that all materials supplied meet applicable pharmaceutical regulations and industry standards.Key ResponsibilitiesCustomer Documentation & Regulatory SupportPrepare, review, and issue technical and regulatory documentation required by pharmaceutical customers, including:Quality & Technical AgreementsSupply Chain StatementsRegulatory QuestionnairesCompliance Statements (e.G., TSE/BSE, GMO, allergens, nitrosamines, residual solvents, elemental impurities)Ensure all documentation is accurate, consistent and aligned with applicable frameworks (i.E. relevant pharmacopoeia, IPEC Guidelines, EU GDP and GMP guidelines.Information Gathering & Supplier EngagementSource regulatory, quality, and technical information internally and from suppliers to fulfil customer requests.Evaluate supplier documentation for completeness, compliance, and suitability for pharmaceutical use.Customer Request ManagementLog, track, and report customer documentation requests using defined KPIs.Support continuous improvement by identifying trends, gaps, and opportunities to streamline documentation processes.Support for Customer Value Added Service ProjectsLead and manage regulatory deliverables for customer-specific projects.Coordinate regulatory assessments, supplier data collection, and compliance documentation for new product introductions or customised specifications.Support change control evaluations and customer notifications.Regulatory Compliance & Standards ImplementationWork with QHSE and supply chain teams to ensure compliance with applicable standards (IPEC GMP/GDP, EXCiPACT, GDP, and other regulatory frameworks).Support implementation of new regulatory requirements and internal standards across the business unit.Cross-Functional CollaborationPartner with commercial and value-added services teams to provide regulatory expertise for customer projects and commercial initiatives.Contribute to global Pharma Regulatory team projects, harmonisation efforts, and continuous improvement activities.Training & Knowledge SharingDeliver training to commercial, supply chain, and internal teams on regulatory topics relevant to supply of materials into the pharmaceutical industry.Act as a subject matter expert for documentation, compliance, and regulatory expectations.Additional ResponsibilitiesPerform any other tasks within capability to support the commercial, regulatory, and compliance success of the Pharma business unit.Your ProfileQualifications & ExperienceDegree in a life science discipline (chemistry, biochemistry, pharmaceutical sciences) or equivalent relevant experience.Strong knowledge of pharmaceutical industry requirements for APIs, excipients, biopharma materials, and traditional pharma raw materials.Understanding of European National Competent Authority requirements for distribution of APIs, excipients, and raw materials.Skills & CompetenciesFluent in English and Spanish (spoken and written).Strong written communication skills with the ability to produce clear, accurate, and compliant documentation.Excellent collaboration skills with the ability to work proactively across all levels and functions.Ability to interpret regulations, resolve compliance issues, and respond to complex regulatory queries.High attention to detail and strong organisational skills.Willingness to undertake occasional travel for customer meetings, supplier visits, audits, or internal workshops. What we offer: The opportunity to join a global industry leader. An international, collaborative, and dynamic work environment. Continuous learning and career development opportunities. The chance to contribute to meaningful projects that make a real impact.Interested in joining us, or know someone who might be a great fit? We'd love to hear from you! Feel free to apply or share this opportunity with your network.Brenntag provides equal employment opportunities to qualified applicants and employees of all backgrounds and identities to create a workplace where difference is valued because it forms a resilient and more innovative organization. We do not discriminate on the basis of age, disability, gender identity, sexual orientation, ethnicity, race, religion or belief, parental and family status, or any other protected characteristic. xhfqzwm We welcome applications from women, men and non-binary candidates of all ethnicities and socio-economic backgrounds.Brenntag TA TeamSummaryLocation: Massalfassar,Spain; Granollers,SpainType: Full time

Oxigent Technologies en Barcelona busca un/a Técnico/a de Cualificación y Validación para integrarse en su planta de Barcelona, participando en proyectos de llenado, cerrado, inspección y packaging en el sector farmacéutico.

Te interesaría seguir desarrollándote como Técnico/a de Cualificación en una sólida compañía en plena expansión internacional? Desde Oxigent Technologies seleccionamos un/a Técnico/a de Cualificación y Validación (IQ, OQ, PQ) para incorporarse en la planta de Barcelona, participando en pr

L'Hospital Sant Joan de Déu Barcelona és un dels centres europeus més importants en les especialitats de Pediatria, Ginecologia i Obstetrícia.El nostre model assistencial compagina la ciència, els avanços tècnics i la humanització, des del respecte a la dignitat de la persona.Recuerde revisa

Enfermero/a de Quirófano (H/M/X) – Barcelona provincia.

Brenntag busca un/a Conductor/a de Camión ADR para la zona de Granollers (Barcelona).

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain.Se anima a todos los posibles solicitantes a que se desplacen y lean la descripción completa del puesto antes de presentar su candidatura.We are a worldwide leader in specialized diagnostics in the areas of He

LolaCasademunt #WeAreHiring #FashionJobs #JuniorFashionDesigner #FashionDesigner #DiseñoDeModa #ModaMujer #FashionCareers #Barcelona #Empleo. Nos interesa especialmente tu mirada sobre la moda, tu capacidad para detectar tendencias y tu potencial para transformarlas en propuestas con personalidad.

Ubicació: BARCELONA - VALLÈS ORIENTAL - 08402 GRANOLLERS. Residencia en Granollers o alrededoresMedio de transporte para desplazarse al trabajo.

Barcelona, Catalonia, Spain | GLOBKSS | Full time FR.Are you passionate about the web and new technology?.If you are tech savvy, creative, outgoing, and willing to roll up your sleeves and get things done in a fast-paced, rapidly changing environment, we may have the perfect job for you!.Teleperfo

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain.Para una comprensión completa de esta oportunidad y de lo que se requerirá para ser un candidato exitoso, siga leyendo.We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Ca

Únete al equipo AniCura! AniCura Lauro Hospital Veterinari en Les Franqueses del Vallès (Barcelona), busca un/a Veterinario Generalista. Qué buscamos? * Experiencia mínima de 1 o 2 años, habiendo trabajado en un hospital veterinario de referencia o haber realizado un internado en uno. AniCura s

Conductor/a de Camión ADR (C+E) - Zona de Granollers (Barcelona).Tienes experiencia en el transporte de mercancías peligrosas y buscas un nuevo reto profesional? En Brenntag estamos buscando dos Conductores/as de Camión ADR para la zona de Granollers (Barcelona), que quiera formar parte de una co

IMAN Global Consulting busca un/a Laboratory Planner para una empresa del sector automoción en Caldes de Montbui (Barcelona).

Persona creativa, organizada, resolutiva y con buena capacidad de comunicación para gestionar la organización de eventos y apoyar las acciones de marketing de diferentes proyectos del grupo con base en Granollers y salidas a Barcelona ciudad, Premià de Mar, etcEl puesto combina organización de e

Nos encontramos en expansión y crecimiento por ello necesitamos incorporar nuevo personal a nuestra plantilla en nuestro centro de GRANOLLERS.

Contrato: Indefinido (20h + 0-10 horas complementarias).Requisito clave: Disponibilidad total para turnos rotativos.Puesto: Encargado/a (posición operativa).Lugar: C/Mare de Deu de Nuria, 22, 08401 (Granollers, Barcelona).Contrato: Indefinido (20h + 0-10 horas complementarias).Requisito clave: Disp

Sumcab Specialcable Group busca un/a Técnico/a Back Office para su delegación de Barcelona, en el departamento IMS.

Sop-Selecci busca un/a Customer Service con Inglés para incorporarse en Cardedeu, dependiente del Responsable del Departamento Comercial. Sus tareas incluyen gestionar ofertas, pedidos y estudios, mantener relación con delegados y comerciales en España, Francia e Internacional, y gestionar CRM y

Técnico/a Laboral con 3–5 años de experiencia en asesoría laboral para unirse a nuestro equipo en la zona de Barcelona/Cardedeu. Entre tus funciones estarán el cálculo y confección de nóminas y seguros sociales, asesoramiento laboral a clientes y la gestión de modelos 111, 115 xcskxlj y 21

Relocation Package: Support available for candidates relocating to Barcelona. Modern workplace in Barcelona's major technology and business hub.

WW Talents in Barcelona seeks a motivated German-speaking B2B Sales Executive to drive new business for an international AI advertising solutions company.

GRUPO CRIT Interim busca un Responsable de Contabilidad para una empresa industrial en el cinturón de Barcelona (Vallés).

En JS Trans, Operador de Transporte en Lliçà de Vall (Barcelona), buscamos mozo de almacén polivalente para puesto mixto de control de rutas y carretillero. Experiencia como coordinador de rutas y carretillero.

Werfen, a global leader in diagnostics with headquarters in Barcelona, seeks a Lab Technician I to participate in manufacturing processes under supervisor direction.Si desea conocer los requisitos para este puesto, siga leyendo para obtener toda la información relevante.You will prepare materials,

CSMIJ Granollers cerca un/a psiquiatre amb experiència en Salut Mental Infanto-Juvenil per atendre pacients i les seves famílies.S’estructurarà un programa d’intervenció i intervenció farmacològica, amb coordinació multidisciplinària i participació en formació continuada.La descripció

Grupo Savia busca un Jefe de Turno para un cliente del sector industrial, ubicado en la Zona del Vallés Oriental (Barcelona). Envíe su CV y cualquier información adicional requerida después de haber leído esta descripción, haciendo clic en el botón de solicitud. Se xcskxlj requiere CFGS en Ma

Bridgestone Granollers, ubicado en Barcelona, busca un/a Mecánico/a de turismo para realizar tareas de neumáticos, mantenimiento, desgastes, diagnóstico y mecánica avanzada en un taller de referencia. Se valorará experiencia en mantenimiento y capacidad para trabajar con flotas y vehículos lig

Realitzarà avaluacions, diagnòstics clínics i intervencions en pacients al centre i hospital de dia, treballant en equip interdisciplinari i contribuïnt al desenvolupament del servei. L'Hospital Sant Joan de Déu Barcelona és un centre de referència en salut mental infanto-juvenil, amb alta es

La empresa líder en el sector de la logística y del transporte del mueble a nivel Europeo, precisa incorporar en su equipo de almacén de Barcelona, a persona operadora de almacén.Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser

En nuestro taller First Stop Granollers de Barcelona, estamos buscando incorporar a un/a Mecánico/a de turismo quien realizará trabajos de neumáticos, mantenimiento, desgaste, diagnósis y mecánica avanzada. Montaje y reparación de neumáticos de turismo.

Brenntag busca un/a Conductor/a de Camión ADR para la zona de Granollers, Barcelona.

Bridgestone, a través de First Stop Granollers en Barcelona, busca incorporar un/a Mecánico/a de turismo para realizar trabajos de neumáticos, mantenimiento y diagnóstico, con posibilidad de desarrollo en un entorno de grupo multinacional.

First Stop Granollers, taller en Barcelona, busca un/a Mecánico/a de turismo para realizar trabajos de neumáticos, mantenimiento, desgaste, diagnóstico y mecánica avanzada.

Prepararinventarios de tienda y realizarpedidos de mercancías con el objetivo de asegurar la disponibilidad delos artículos y ajustar las cantidades al consumo real, mediantelas herramientas de apoyo. Desarrollar y optimizar los procesos operativos de la tienda. Presentar e implementar los Informe

Buscamos promotor/a con perfil muy comercial para promocionar e incentivar la venta de una conocida marca de tabaco a las personas fumadoras de distintos estancos de toda la provincia de BARCELONA. Experiencia previa como comercial o promotor/a de estancos.

Buscamos un/a Area Sales Manager / Responsable Comercial Regional para desarrollar negocio en Catalunya dentro del sector de productos eléctricos.Es esencial asegurarse de que cumple con los requisitos como solicitante para este puesto; por favor, lea atentamente la información a continuación.La