Jobs in Santa Perpetua De Moguda - Page 6Create job alertsNo experience

En Montornès del Vallès se necesita una persona para trabajar como guillotinista de papel y cartón en una empresa del sector industrial.Se busca alguien con experiencia en guillotinas industriales, responsable, dinámico y polivalente, que quiera incorporarse a un proyecto estable.Las tareas prin

El flujo de trabajo sigue un proceso ordenado, desde la preparación de las piezas hasta el montaje final y la inspección de calidad. El puesto implica el ensamblaje y montaje integral de los muebles y estructuras interiores para baños de trenes. Una parte fundamental del trabajo es la capacidad d

El puesto de Operario de Carretilla Elevadora se centra en las tareas logísticas esenciales dentro de un entorno industrial.La función principal implica la manipulación y organización eficiente de mercancías, asegurando que los procesos de almacén se desarrollen con fluidez y precisión.Las re

Associate Director, Enterprise Security Architecture - Network. The Associate Director, Enterprise Architect Network Security will contribute to the development of Network Security architectural standards, and the direction and design of architecture for a business or technical domain, and contribut

Grifols, a global leader in healthcare, is seeking a Manufacturing Engineer for its Diagnostic Grifols SA unit in Parets del Vallès, Spain. The role focuses on leading projects to install and upgrade manufacturing equipment, facilities and production areas within GMP environments. You will collaborate with Manufacturing, Quality, Validation and Maintenance teams, drive continuous improvement, and coordinate with external engineering firms to meet timelines and budgets. #J-18808-Ljbffr

Se busca vendedor interiorista con experiencia en reformas, cocinas, baños y materiales de construcción.

Spain is seeking an AI Solutions Analyst to identify, design and implement AI-driven processes within the Microsoft 365, Copilot Studio, Power Platform ecosystem.You will translate business challenges into scalable low-code solutions while ensuring governance and compliance across the organization.E

Se busca un profesional para el puesto de charcutero o charcutera en Parets del Vallès, dentro del sector de la alimentación.

Volpak, part of Coesia, is seeking an experienced R&D Engineering Lead based in Santa Perpètua de Mogoda, Spain. You will guide the engineering team to design and verify packaging machinery modules, ensuring alignment with technical requirements and production release deliverables. You will collaborate with Mechanical, Hardware and Software teams, manage KPIs, drive Design to Cost initiatives, and support manufacturing while traveling up to 20% worldwide when needed. #J-18808-Ljbffr

We are seeking a detail-oriented Plumbing Engineer to join our team, assisting in the preparation of plumbing system construction documents for healthcare, higher education, and commercial building projects. The Plumbing Engineer will collaborate with project teams throughout the design and construction phases, ensuring plumbing plans align with budget constraints, design requirements, and client needs. This role includes staying up-to-date with industry trends, attending professional development events, and fostering connections with local industry professionals. KEY RESPONSIBILITIES: Perform technical design and quality control on assigned projects, including plumbing system calculations and layouts. Coordinate designs with other disciplines to ensure seamless integration. Maintain best practices in engineering methods and ensure compliance with current plumbing and energy codes. Produce construction documents for new builds, renovations, and facility additions. Conduct construction administration, including site visits and shop drawing reviews. Explore and implement cost-efficiency improvements in plumbing designs. Develop and review project specifications. Update and correct drawings based on quality assurance feedback. Assist the director in maintaining quality assurance standards. EDUCATION AND EXPERIENCE: Education: Bachelors Degree in Architectural or Mechanical Engineering from an ABET-accredited program. Experience: 35 years in the engineering field with expertise in plumbing systems. Experience with medical gas systems (preferred). Related experience in healthcare, higher education, or commercial building system design. Knowledge of current plumbing and energy codes. Project management experience is a plus but not required. CERTIFICATIONS AND LICENSES: Fundamentals of Engineering (FE) Exam required. Professional Engineering (PE) license preferred but not required. Valid drivers license and willingness to use an insured personal vehicle for work-related travel. SKILLS AND QUALIFICATIONS: Proficiency in Microsoft Office , AutoCAD , and Revit . Strong verbal and written communication skills. Exceptional organizational skills and attention to detail. Effective time management and multitasking abilities to meet project deadlines. Ability to work collaboratively within a team-oriented environment. Candidates must be legally authorized to work permanently in the country where the position is located without the need for sponsorship. WHY JOIN US? This role offers an exciting opportunity to work on impactful projects within a collaborative and innovative environment. The ideal candidate will have access to professional development resources and the chance to implement creative and cost-efficient solutions in plumbing design. Equal Opportunity Employer/Veterans/Disabled: We are an Equal Opportunity Employer committed to diversity and inclusion. Reasonable accommodations will be provided to individuals with disabilities to ensure they can perform essential job functions. If you are a driven and detail-oriented professional with a passion for engineering excellence, we encourage you to apply! #J-18808-Ljbffr

INDIBA is a global medical device company focused on RF solutions for physiotherapy, aesthetics and veterinary markets. We are seeking a senior finance professional to join the Group Controller and CFO teams to support accounting, audit, consolidation, tax, treasury and finance projects. You will analyse complex financial matters, coordinate external audits, drive cash flow forecasting and lead finance transformation initiatives across the international group. #J-18808-Ljbffr

INDIBA is a global medical device company in the field of Radiofrequency (RF) solutions for the physiotherapy, aesthetic and veterinary markets, and is known worldwide for the scientific research performed over the last 40 years. INDIBA is a global medical device company in the field of Radiofrequency (RF) solutions for the physiotherapy, aesthetic and veterinary markets, and is known worldwide for the scientific research performed over the last 40 years. At INDIBA, we believe we can contribute to the health and well-being of our patients by addressing new and growing needs, offering treatments that allow people to continue enjoying their lifestyle as they grow older and animals too. Revitalizing lives is what we do and what our Research & Development teams work towards every day. We are actively seeking a Group Finance Specialist / Senior Finance Manager to join our Finance team in Sant Quirze del Vallès (Barcelona). Reporting to the Group Controller and working closely with the CFO , this role will support INDIBA’s growth and international expansion across accounting, audit, consolidation, tax, treasury and finance projects. We are looking for a senior finance problem solver with a strong technical background, able to analyse complex financial matters, structure solutions and provide practical recommendations across the Group. • Act as a finance problem solver across the Group, analysing complex financial matters and providing practical recommendations., • Support Group accounting, consolidation and financial reporting, including technical accounting matters related to acquisitions and business combinations., • Coordinate external audits and act as a key contact for auditors and external advisors., • Support corporate tax and Transfer Pricing matters, coordinating with external advisors and international subsidiaries., • Lead cash flow forecasting and treasury planning, monitoring liquidity and working capital performance., • Provide financial analysis and scenario modelling to support management decision-making., • Drive finance transformation and process improvement initiatives, including automation, reporting tools and financial controls., • 8+ years of relevant experience in finance, accounting or audit, ideally combining Big Four audit experience with a multinational or international environment., • Strong knowledge of accounting, financial reporting and consolidation, including IFRS and/or Spanish GAAP (PGC)., • Experience in audit coordination, corporate tax, Transfer Pricing, treasury and cash flow forecasting., • Exposure to acquisitions, business combinations or integration projects will be highly valued., • Bachelor's degree in Finance, Accounting, Economics, Business Administration or a related field., • Advanced Excel skills and experience with ERP systems; Power BI knowledge is a plus., • Professional proficiency in English and Spanish., • Strong analytical and problem-solving skills, with a hands‑on, autonomous and continuous improvement mindset. #J-18808-Ljbffr

Energiot is seeking a Mechanical Design Engineer to enhance its product and R&D team in Barcelona. This role focuses on the mechanical design of IoT devices for monitoring electrical networks, including development of parts, tooling, prototypes, and manufacturable solutions. The ideal candidate will have at least 5 years of experience in mechanical design, proficiency in SolidWorks, and strong communication skills in Spanish and English. We offer a full-time contract, private medical insurance, and a dynamic startup culture focused on innovation. #J-18808-Ljbffr

Se precisa profesional para la colocación de pavimento laminado en la localidad de Santa Perpètua de Mogoda, en la provincia de Barcelona. La persona seleccionada se encargará de la instalación del material, asegurando la correcta nivelación, el ajuste de las piezas y el acabado final conforme a las especificaciones del proyecto. No se requiere formación específica para desempeñar las tareas, aunque se valorará la experiencia previa en trabajos de colocación de pavimento laminado. Se considera deseable disponer de vehículo propio para los desplazamientos al lugar de trabajo, así como contar con el carnet de conducir tipo B para coches y vehículos ligeros. La incorporación está prevista de forma inmediata. Las personas interesadas pueden remitir su solicitud a través del medio indicado en esta página web, adjuntando la información que consideren relevante sobre su trayectoria en el sector.

INDIBA Group is seeking a Regulatory Affairs Specialist to join our Sant Quirze del Vallès office.You will manage regulatory approvals worldwide for medical devices and cosmetics, ensuring compliance and timely submissions.Qualifications include a degree in health sciences or related field, 3+ year

Lhh busca un Responsable de Administración en Montmeló para liderar un equipo y gestionar la administración y control de costos de proyectos.Es usted el solicitante adecuado para esta oportunidad? Descúbralo leyendo el resumen del puesto a continuación.Los candidatos deberán tener experiencia

Louis Vuitton en Barberà del Vallés busca un/a Jefe/a de Sección para liderar un equipo de marroquineros y garantizar el logro de los objetivos de producción. Coordinará con otros departamentos y supervisará el proceso de su sección para asegurar eficiencia y calidad. El candidato ideal cuenta con más de 3 años de experiencia gestionando equipos en entornos industriales y un grado en Ingeniería Industrial u afín. Ofrecemos desarrollo profesional, onboarding y beneficios variados. #J-18808-Ljbffr

Responsable administración Montmeló Compañía: Grupo constructor dedicado a proyectos de edificación y obra civil, con presencia tanto en el ámbito público como privado.

Do You Want to Be Part of a Company Committed to Shaping a Brighter Future for Us All? Are you eager to identify opportunities for improvement, challenge the status quo, and drive meaningful change? If so, we would love to hear from you. We are looking for a Global Key Account Manager Offshore Wind to play a key role in developing and executing global account strategies and operational plans to drive sustainable and profitable growth across the Offshore Wind value chain. The role combines strategic Global Account Management of key offshore asset owners with Global Project Management of selected strategic projects, driving early customer engagement, cross-functional collaboration and increased win rates. This exciting reports directly to Head of Global Key Account Management Renewables and works closely with a wide range of global stakeholders, including R&D, Solutions Management, Sales, Service, Operations, Quality, Finance, Legal and Supply Chain. This is your opportunity to make a meaningful impact on Hempel’s market leadership and build long-term, value-adding partnerships with strategic customers. Do You Want to Work in an Environment Where All Voices Are Respected? In This Role, You Will Drive global account growth and customer success by managing strategic key accounts, building long-term customer partnerships, and identifying opportunities to increase revenue, profitability, and market share. Lead high-value global projects from opportunity identification and qualification through bidding, execution, and successful delivery, ensuring strong commercial and customer outcomes. Develop and execute winning commercial strategies, including customer engagement plans, value propositions, pricing strategies, stakeholder mapping, and competitive positioning to secure new business and strengthen customer loyalty. Collaborate across a global organization, bringing together Sales, R&D, Technical Service, Supply Chain, Finance, Legal, and other teams to deliver seamless customer solutions and achieve project objectives. Ensure commercial excellence and continuous improvement through effective pipeline management, forecasting, risk mitigation, performance tracking, market intelligence, and the identification of new growth opportunities while maintaining the highest standards of quality, safety, and compliance. Do You Dream of Working in a Culture of Inclusion, Transparency, and Support? Here’s what it takes to become our next team member Degree or equivalent relevant professional experience. Minimum 5 years' experience in commercial, sales, account or project management roles; Offshore Wind, Wind Energy, Coatings, Engineering or Fabrication experience preferred. Proven track record in global account management, complex sales and/or project management. Strong experience working across functions, regions and cultures. Experience with CRM, pipeline management, forecasting and project governance. PMP, PRINCE2, NACE/FROSIO or similar certification is an advantage. Fluent English; additional relevant languages are an advantage. Open to travel. Experience, attitude and behavior are considered at least as important as formal education. This role requires a commercially driven professional with strong project management capabilities and a proven ability to lead and influence diverse stakeholders without formal authority. The successful candidate combines strategic thinking with hands-on execution, excels at simplifying complexity, prioritizing high-impact activities, and driving value through effective negotiation and customer engagement. Strong communication, presentation, networking, and stakeholder management skills are essential, including the ability to engage confidently at C-suite level. The role also demands disciplined CRM and forecasting practices, excellent collaboration in a global and multicultural environment, clear communication of project progress and risks, and a strong commitment to quality, safety, and continuous improvement. Application due 2026-10-28 Seniority Level Mid-Senior level Job Functions Business Development, Consulting, Sales Industry Chemicals At Hempel, you’re welcomed to a global community of +7000 colleagues around the world. A workplace built on shared trust, mutual respect and support for each other. We’re on a mission to double our impact. To succeed, we need bright minds and team players. Which is why, from day one, your input, ideas and initiative are not only welcomed, but expected. In return,you will enjoy great opportunities for development in a growing global company – and be part of the solution by contributing to our global impact. At Hempel, we are committed to everyone feeling safe, valued and treated equally, in an environment where each employee can bring their authentic selves to work. We believe that inclusion is key to innovation and by bringing together the most diverse perspectives and talents, we can achieve great things, together. #J-18808-Ljbffr

Noucor, compañía químico-farmacéutica, busca un Direct Category Buyer para liderar la estrategia de compras de packaging farmacéutico y servicios de CMO, alineada a las necesidades del negocio. Serás responsable de negociar con proveedores, gestionar categorías estratégicas y asegurar el cumplimiento regulatorio, impulsando la eficiencia y la sostenibilidad en la cadena de suministro en un entorno internacional. #J-18808-Ljbffr

Spain and Portugal for sales force roles.

HARTMANN Montornés del Vallés busca un Engineering Project Manager para liderar la implementación de proyectos en una planta de producción con enfoque LEAN y tecnología puntera. Serás responsable de la planificación, coste y recursos, así como del liderazgo técnico desde definición hasta ejecución del proyecto, garantizando la entrega en tiempo y alcance. Formarás parte de un equipo con alto conocimiento técnico y trabajarás estrechamente con proveedores, marketing, finanzas y RRHH para impulsar #J-18808-Ljbffr

At BOLD, we design and build the next generation of high-performance battery systems for the world’s most demanding industries — from Formula 1 and hypercars to aerospace, marine and defense. Our mission: to deliver energy systems where every millisecond and every degree matter. What You’ll Do Industrialisation & Production Lines Define the technical concept of battery pack production lines, from prototype builds to niche-volume production. Develop and optimise manufacturing processes for assembly, welding, and end-of-line (EOL) testing. Ensure production solutions meet quality, safety, scalability, and manufacturability requirements. Support the definition of plant layouts, production flows, and manufacturing concepts. Provide technical support during equipment commissioning, process validation, and production ramp-up. Engineering & Product Design Collaboration Collaborate closely with engineering teams to ensure product designs are optimised for manufacturability. Recommend design improvements to enhance production efficiency, product quality, and cost-effectiveness. Align product requirements with manufacturing capabilities and process constraints. Support the definition of fixtures, tooling, and material handling solutions. Identify and mitigate industrialisation risks during the early stages of product development. Supplier & Automation Management Coordinate with equipment suppliers and automation integrators throughout project execution. Define technical requirements and specifications for manufacturing equipment and automation systems. Provide technical support during equipment manufacturing, installation, commissioning, and validation. Ensure the successful integration of automated and semi-automated production systems. Review and validate technical solutions from both manufacturing and quality perspectives. Quality, Process & Continuous Improvement Ensure manufacturing processes comply with applicable quality standards, including IATF 16949 or equivalent. Support the implementation of quality control, traceability, and process monitoring systems. Contribute to the definition of control plans, process validation, and production readiness activities. Drive continuous improvement initiatives to enhance process efficiency, reliability, and repeatability. Investigate and resolve manufacturing and process-related technical issues to support stable production. Requisitos mínimos What You Bring 5+ years of experience as a Process Engineer, Manufacturing Engineer, or in a similar role within an industrial manufacturing environment. Bachelor’s or Master’s degree in Industrial, Mechanical, Electronic, Automotive Engineering, or a related discipline. Hands‑on experience with battery pack manufacturing processes, from prototype builds to low‑/medium‑volume production. Strong knowledge of assembly, welding, and end‑of‑line (EOL) testing processes. Experience specifying and implementing industrial automation systems and production equipment. Expertise in the design and validation of tooling, fixtures, and material handling systems. Solid understanding of industrial quality systems, process validation, and manufacturing in regulated environments. Knowledge of IATF 16949 quality standards (preferred) and ISO 9001. Black Level certification (Second Intervention Team – Emergency Response). Red Level certification (High‑voltage battery handling and electrical safety training). Why Join BOLD High-growth, multicultural environment: Be part of a fast-scaling company driving innovation in advanced electrification. Competitive Compensations Life Insurance Private health insurance - Reduced cost for employees and family. Subsidised canteen Flexible work schedule and up to 5 remote days/month. Monthly Town Hall About BOLD At Bold, we’re a diverse, international team with backgrounds in automotive, motorsport, aerospace, defense and aviation. We combine creativity and engineering rigour to deliver high-performance, safe and sustainable energy systems for the world’s most demanding applications. We Operate Through Two Divisions BOLD Applied Engineering (BAE )– Provides top-tier professional engineering services, primarily to elite motorsport teams (especially Formula 1), in areas such as composite design, mechanical engineering, aerodynamics and systems integration. This expertise is transferred directly to complex defence sector programmes. BOLD Technology (BT) – Designs, develops and manufactures high‑voltage battery systems and electric propulsion system components for defence applications, tactical vehicles, military platforms, aviation and advanced mobility. BOLD is an international benchmark in defence electrification, supplying systems to United States Army programmes and collaborating with leading defence primes in the US and Europe. Inclusion & Diversity BOLD is an equal opportunity employer. We foster a culture where ideas thrive based on merit and competence, regardless of age, disability, race, religion, gender, sexual orientation, or family circumstances. Privacy Policy BOLD respects your privacy and is committed to protecting the personal information you share with us, please refer to Bold’s Privacy Policy for more details. #J-18808-Ljbffr

Boehringer Ingelheim operates an extensive Salesforce.com (SFDC) landscape in a global multi-org ecosystem across various integrated solutions such as Veeva CRM, Patient Support programs, Digital Marketing engagements, and custom applications for business operations. As a Solution Engineer within the Salesforce Centre of Excellence (CoE) team, you will bring your technical skills and knowledge to facilitate requirement gathering, explore possible recommendations within the Salesforce technology and capabilities, deliver potential solutions via prototypes and proof of concepts, and facilitate adoption and usage of the Salesforce platform across Boehringer. It includes being involved in multiple projects and initiatives to digitalize business processes, engaging with key stakeholders across IT and business, and collaborating within the Salesforce CoE to improve processes and deliver value with the Salesforce platform. Tasks and responsibilities Platform Leadership: Partner with IT teams and colleagues to provide functional and technical guidance and ensure successful implementation of projects and initiatives, including supporting the architectural design review of the Salesforce ecosystem. Technology & Innovation: Evaluate business needs and requirements, and recommend existing and/or emerging Salesforce technologies and tools to develop potential solutions for new development and/or enhancements, incorporating user experience and customer centric perspective to ensure that solutions are delivered to improve operational and process efficiency. Solution Enablement: Develop solutions including prototypes, proof of concepts, and solution designs to leverage the functionalities and capabilities of the Salesforce platform. Build solutions to deliver business needs, drive adoption within the organization, and expand the Salesforce ecosystem. Delivery & Support: Collaborate with the Salesforce CoE team to facilitate and perform existing platform processes and activities (review, assess, deploy, and maintain). Identify and provide insights and improvement opportunities to the team. Engineering Excellence: Facilitate and co-govern development standards, code quality, and best practices on the Salesforce platform. Requirements Bachelor's degree in Computer Science, Software Engineering, or related field (Master’s degree is a plus) Proven experience as a Solution Engineer in the Salesforce ecosystem with in-depth understanding of the Salesforce technology and solutions, including effective use of low-code/no-code configuration and data integration implementation Experienced in collaborating with development teams and delivering solutions through different development methodologies (Agile/Scrum, Waterfall, DevOps) Proficient in Flow, Trigger, Apex, Lightning Web Component, Integration Knowledge in Sales Cloud, Service Cloud, Experience Cloud, Data Cloud, Marketing Cloud, and Agentforce Solution-oriented to resolve business and operational challenges efficiently with practical, innovative, and scalable solutions Curious to learn and explore new technologies to solve business challenges and to exhibit critical and analytical approaches to support stakeholders in identifying possible Salesforce solutions Effective written and verbal communication skills, able to articulate clearly with different stakeholders on complex subjects Effective presentation and alignment skills with functional and technical architects, developers, and business users Please note: The job title used in this advertisement may differ from the official contractual title. We are continuously working to design the best experience for you. Here are some examples of how we will take care of you: Flexible working conditions Life and accident insurance Health insurance at a competitive price Investment in your learning and development #J-18808-Ljbffr

Taller de mecanizados ubicado en Sabadell, con más de treinta años de experiencia en el sector metalúrgico, trabajando para la Industria del packaging y cualquier tipo de maquinaria, somos especialistas en series cortas y medias.Contamos con personal cualificado, maquinaria moderna, Fresas CNC y

We are seeking a detail-oriented Plumbing Engineer to join our team, assisting in the preparation of plumbing system construction documents for healthcare, higher education, and commercial building projects. The Plumbing Engineer will collaborate with project teams throughout the design and construction phases, ensuring plumbing plans align with budget constraints, design requirements, and client needs. This role includes staying up-to-date with industry trends, attending professional development events, and fostering connections with local industry professionals. • Perform technical design and quality control on assigned projects, including plumbing system calculations and layouts., • Coordinate designs with other disciplines to ensure seamless integration., • Maintain best practices in engineering methods and ensure compliance with current plumbing and energy codes., • Produce construction documents for new builds, renovations, and facility additions., • Conduct construction administration, including site visits and shop drawing reviews., • Explore and implement cost-efficiency improvements in plumbing designs., • Develop and review project specifications., • Update and correct drawings based on quality assurance feedback., • Assist the director in maintaining quality assurance standards., • Education: Bachelors Degree in Architectural or Mechanical Engineering from an ABET-accredited program., • Experience:, • 35 years in the engineering field with expertise in plumbing systems., • Experience with medical gas systems (preferred)., • Related experience in healthcare, higher education, or commercial building system design., • Knowledge of current plumbing and energy codes., • Project management experience is a plus but not required., • Fundamentals of Engineering (FE) Exam required., • Professional Engineering (PE) license preferred but not required., • Valid drivers license and willingness to use an insured personal vehicle for work-related travel., • Proficiency in Microsoft Office , AutoCAD , and Revit ., • Strong verbal and written communication skills., • Exceptional organizational skills and attention to detail., • Effective time management and multitasking abilities to meet project deadlines., • Ability to work collaboratively within a team-oriented environment., • Candidates must be legally authorized to work permanently in the country where the position is located without the need for sponsorship. This role offers an exciting opportunity to work on impactful projects within a collaborative and innovative environment. The ideal candidate will have access to professional development resources and the chance to implement creative and cost-efficient solutions in plumbing design. Equal Opportunity Employer/Veterans/Disabled: We are an Equal Opportunity Employer committed to diversity and inclusion. Reasonable accommodations will be provided to individuals with disabilities to ensure they can perform essential job functions. If you are a driven and detail-oriented professional with a passion for engineering excellence, we encourage you to apply! #J-18808-Ljbffr

Novartis Farmacéutica, S.A. is seeking a Trial Vendor Manager to lead the Clinical Trial Team's vendor sub-workstream, overseeing vendor service delivery, study timelines, budgets, quality, and compliance.The role partners with the Vendor Start-up Manager across labs, IRT, eCOA/ePRO, imaging and PR&R to ensure timely study initiation. You will manage vendor-related risks, translate protocols into vendor specifications, supervise UAT for eCOA/IRT, and drive site activation from a vendor

Se busca Arquitecto/a de Soluciones para transformar necesidades de negocio en soluciones tecnológicas escalables y robustas, colaborando con equipos de desarrollo y participando en decisiones estratégicas.

BOLD is committed to shaping the future of high-performance mobility from Formula 1 to aviation and marine. In our mission to deliver innovative and impactful products in the mobility sector, we are building the company whilst working with clients in exciting engineering and manufacturing challenges. The Technical Buyer will be responsible for driving and developing all activities related to the procurement of components for our battery and electrification technologies, with a focus on electrical/electronic components (PCBA, HV Electrical distribution). About Bold Valuable Tech: Our Vision At Bold, we´re a diverse community, from all over the world and from multiple industries and backgrounds. Combining experience from Automotive, Motorsport, Aerospace and Aviation with skills from concept phase through to full product delivery. Our rapid expansion is a testament to our commitment to pushing boundaries and delivering cutting‑edge solutions. We have two engineering divisions, different in their technologies but similarly focused on delivering compelling products to our customers. In our Applied Engineering division, we are an integral part of the design & development process for our high‑performance customers including Formula 1, Motorsport and Automotive. From the initial stages of blank sheet designs to the final production, we assume ownership with a relentless commitment to bringing our clients' visions to life. We contribute across all areas of engineering and in multiple different specialisms including composite & materials, bodywork, aero & structural, powertrain, and tooling. In our Technology division, we specialize in R&D of state of the art of battery systems. Taking projects from initial concepts to production: we are designing, developing, testing, and manufacturing the next generation of high‑performance batteries to innovative projects for multiple industries. We aim to generate a real impact on the future of electric mobility. Responsibilities Manage all purchases, both direct and indirect: electronic components, props, industrial products, work materials, supplies and other products or services. Logistics and transport: negotiate with logistics providers for the distribution of products. Support in negotiating contracts, prices and terms with suppliers. Ensure that products and materials purchased comply with technical and quality specifications. Collaborate with the engineering and production teams to ensure that purchased products meet technical requirements. Work on cost saving initiatives and search for alternative suppliers. Identify and evaluate new strategic suppliers for key raw materials. Develop and maintain long‑term relationships with suppliers. Continuous assessment of suppliers' capabilities, risks and performance to ensure continuity of supply. Standardisation of processes and documents. Create and manage the RFI/RFP/RFQ process. Compensation And Benefits Competitive compensation. Flexible compensation, which includes Health insurance and Kindergarten. Dining room & subsidized catering. Flexible Work Schedule. BOLD is an equal opportunity company. We believe in a merit and competence culture where the best ideas thrive regardless of age, disability, race, religion, or belief, gender, sexual orientation, marital status or family circumstances. Bold respects your privacy and is committed to protecting the personal information you share with us, please refer to Bold’s Privacy Policy for more details. Minimum Requirements Advanced university degree in Engineering or Finance. 5 years of experience in procurement of industrial components and materials (automotive, electronics, plastic parts and structural metals, PCBA, high voltage electrical distribution). Extensive user level experience in ERP systems, preferably Odoo. Extensive experience in negotiation with suppliers. In‑depth knowledge of local national and European markets. Experience in implementing improvements and standardisation of Supply Chain processes. Previous experience in battery technology with a wide range of trading groups and both low and high value commodities (direct and indirect). #J-18808-Ljbffr

Soporte en la gestión, control y desarrollo de sistemas de calidad industrial, gestionando no conformidades, contactando con clientes y realizando auditorías internas.

El puesto de montaje industrial se desarrolla en el sector del metal, en Barberà del Vallès, dentro de un entorno de taller dedicado al montaje, mantenimiento y reparación de vehículos industriales y sus componentes, como carrocerías, plataformas elevadoras y equipos de frío para camiones.El t

Salary Range: €69,100.00 - €128,300.00 Job Description Summary #LI-Hybrid Location: Barcelona, Spain This role is based in Barcelona, Spain. Novartis is unable to offer relocation support for this role. Please only apply if this location is accessible for you. The Regional PV QA Head provides end to end quality assurance vigilance expertise and support to global and local operational Pharmacovigilance (PV) and Device Vigilance activities within Novartis with a focus on the country organizations, as well as quality expertise in regional and local vigilance regulation, in order to ensure compliance with applicable regulatory requirements and Novartis procedures. Job Description Drive independently the regional and country quality oversight for implementation and maintenance of Novartis vigilance Quality Systems performed by the local teams, namely Quality Issue, proactive risk assessment and action management systems. Ensure, together with PS and PV in Countries and Regions team, that regional and country quality performance of the Novartis Vigilance System tasks and responsibilities is performed as required under global, regional and country PV regulations, to monitor that safety of the Novartis authorized products are met, and changes to their risk-benefit balance are identified. Support the regional and country Global Research and Development Quality management cycle through development, execution and accountability for deliverables of the global vigilance Quality Plan (QP). Coordinate execution of the QP with relevance to applicable regional and country patient safety activities and report the status to applicable Global PV QA team. Monitor indicators that relate to the performance, compliance and quality of regional and country vigilance systems, in line with indicators defined by Global PV QA team. Act as a quality champion by communicating risks to PS and PV and providing recommendations on potential mitigations. Promptly communicate regional and country compliance issues to Global PS&PV, PV QA management and QPPV. Proactively propose potential quality improvement measures and develop strategies aimed at simplifying processes and improving quality of outputs while ensuring compliance with regulatory requirements; share best practice within and across regions. Lead regional initiatives focused on quality improvement and compliance, provide ongoing project support and governance, as assigned. Provide expertise and support Global PV QA team in the execution of vigilance Quality Risk Assessments (QRA) to identify and mitigate regional and country PV risks. Support maintenance of the Novartis global Pharmacovigilance System Master File (PSMF), where applicable. Ensure a constant state of regional and country vigilance inspection readiness. In line with Global PV QA and PS&PV teams, prepare for, facilitate, provide expertise and lead logistics for Health Authority (HA) vigilance inspections, assess results of pre-inspection activities and HA inspection findings in terms of associated risks and communicate to management. Perform Quality check of vigilance inspection deliverables. Align with PS and PV team and review the inspection corrective and preventive (CAPA) plan, to ensure quality, consistency and appropriateness of commitments. Act as the functional QA approver of inspection CAPA plans from the PV inspections in country organizations in the QMS. Monitor the status of implementation of the CAPAs and approve the related evidence in the QMS, to ensure they are completed, appropriately documented and sustainable. Expertly guide the development of robust and sustainable CAPAs to address PV audit findings related to country organizations and act as functional QA approver of the CAPA plan in the QMS. Monitor the status of implementation of CAPAs to ensure they are completed, appropriately documented and sustainable and approve applicable related evidence in the QMS. Provide expertise and support country PS and PV and other business partners with identification and compliance of-Quality Issue investigations, act as functional QA in the QMS and ensure timely escalation of applicable Quality Issues to management; provide assistance in the remediation of PV system issues; ensure follow-up and monitoring of completeness of CAPAs in alignment with PV QA team. Oversee definition of PV self-assessment plans from Regional PS & PV team to regional and country pharmacovigilance processes as well as their execution. Review vigilance self-assessment reports and approve related action plans in the QMS. Identify regional and local training needs (for example via Quality Issues) and deliver knowledge sharing sessions that meet the needs of business and QA partners and improve overall quality and compliance of the Vigilance system. Provide guidance and recommendations on Merger & Acquisition as well as divestment relevant activities for integration or disintegration of the vigilance system, where applicable. Lead and/or support due diligence (DD) activities for potential product and/or company acquisitions, when applicable. Minimum Requirements Degree in Life Sciences or related scientific discipline. Higher degree desirable. Excellent written and verbal English communication skills; fluency in a second language a plus. Quality/ PV/ clinical/ regulatory affairs/ pharmaceutical industry/ health authority experience; GCP/PV/GMP auditing or inspection experience and Health Authority interactions a plus. Experience in PV in a country organization and global quality support to stakeholders in country organizations a plus. Ability to travel up to 20%. Ability to independently manage and objectively evaluate complex compliance issues with minimal supervision; Excellent problemsolving, decision making and prioritization skills. Quality mindset and excellent quality and compliance leadership and facilitation skills. Extensive knowledge of PV regulations, guidelines and policies; Awareness of GCP and Part 11 requirements. Ability to lead teams and operate successfully in various team capacities and diverse cultural environments. Ability to deputize for the Global Head PV QA Regions and Countries as needed. Benefits & Rewards At Novartis, we’re committed to reimagining medicine together - and rewarding the people that make it happen! Expected Annual Base Salary Range for role: 69,100.00 -128,300.00 EUR The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. Read our brochure to learn more about our global total rewards offering: Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. Skills Desired Business Acumen, Business Partnerships, Change Management, Communication, Continuous Improvement, Data Integrity, Digital Fluency, Ensure Compliance, GMP Operations, Good Laboratory Practices (GLPs), Good Manufacturing Practices (GMP), Leadership, Managing Ambiguity, Organizational Savvy, Problem Solving, Process Improvements, Quality Assurance (QA), Quality Compliance, Quality Management (QMS), Regulatory Compliance, Risk Management, Stakeholder Management, Storytelling, Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. #J-18808-Ljbffr

L’equip de salut mental infantil i juvenil del Consorci Corporació Sanitària Parc Taulí dona atenció integrada a tots els nens i adolescents amb trastorns mentals o en situació de risc des del moment en que es detecta i amb continuïtat assistencial amb dispositius sanitaris, educatius i socials de la comunitat. El nostre model d’atenció és bàsicament comunitari, tenim atenció ambulatòria, en dos CSMIJs, un programa de suport a l’autisme a les escoles (AIS i SIEIS) i suport a la patologia mental greu a l’escola en el programa MAPA. També hem desenvolupat el programa salut i escola, i col·laborem en la formació a EAPS, orientadors i mestres. Disposem també de programes específics al CSMIJs: programa d’autisme (TEAm), primers episodis psicòtics (PEPs), trastorns de la conducta alimentària (TCA), Malalties Minoritàries, SAF, consum de tòxics en adolescents i el programa de suport a la DGAIA. Disposem d’una planta d’hospitalització per psiquiatria infantil, hospital de dia general de salut mental infantil i juvenil i hospital de dia específic de trastorns de la conducta alimentària. Som un equip majoritàriament jove i motivat, amb projecció docent i investigadora. Estem integrats en un Hospital Universitari amb una Unitat Docent de la Universitat Autònoma de Barcelona. Formem part de la Unitat Docent Multiprofessional en Salut Mental en la que tenim la responsabilitat en la formació específica infanto-juvenil de metges, psiquiatres infantils, psicòlegs clínics i infermers en formació, tant del nostre hospital com d’altres hospitals de Catalunya. Principals responsabilitats:Funcions assistencials:Primeres visites de pacients en règim ambulatori, anàlisi del motiu de consulta i presa de decisió sobre el pla d’intervenció i la prioritat.Visites de seguiment dels pacients atesos.Entrevistes diagnòstiques en pacients i les seves famílies.Avaluació psicològica, psicomètrica i neuropsicològica de la intel·ligència, de la personalitat, dels principals trastorns mentals i del comportament en pacients infanto-juvenils.Diagnòstic diferencial i criteris de derivació a altres especialistes.Elaboració d’informes psicològics.Presentació, participació activa i discussió en les sessions clíniques.Tractament psicoterapèutic individualitzat.Intervencions familiars.Interconsulta psicològica amb altres professionals de la salut (atenció primària).Coordinació amb professionals d’altres serveis (educació, serveis socials).Elaboració i realització d’un programa grupal en població infanto-juvenil i/o les seves famílies. Quins requisits són necessaris?Títol de Llicenciatura/Grau en Psicologia.Títol d’Especialista en Psicologia Clínica.Nivell de català C1 o compromís d’obtenir-lo en el termini de tres anys*. Es valorarà positivament:Trajectòria curricular.Formació continuada en atenció a la salut mental en infanto-juvenil.Experiència en salut mental comunitària.Experiència clínica en psicologia infantil.Capacitat per col·laborar amb els diferents dispositius de l’entorn de Salut Mental Infanto-Juvenil, addiccions, recursos acadèmics, recursos comunitaris de salut i socials.Capacitat de treball en equips multidisciplinaris, de comunicació i empatia vers els usuaris, els familiars i els professionals. Busquem una persona amb:Habilitats comunicatives: comunicació efectiva, clara, empàtica i assertiva amb usuaris, famílies i amb la resta de professionals de l’equip.Responsabilitat: alt compromís ètic i professional, capacitat de prendre decisions i executar les funcions del lloc de feina des de la implicació i l’atenció de qualitat, tenint en compte els requeriments i les indicacions rebudes i els criteris propis d’actuació. Capacitat de reflexió crítica per millorar contínuament l’atenció prestada.Treball en equip: treballar de forma cooperativa i coordinada amb totes les persones que formen un equip, col·laborant en la realització de les tasques i entenent que es treballa per a un objectiu comú i una visió interdisciplinàriaAdaptabilitat: capacitat de cercar i aplicar respostes àgils i eficaces davant de situacions, entorns, persones, responsabilitats i tasques canviants, integrant el canvi de manera positiva i constructiva.Predisposició a l’aprenentatge: mantenir una actitud positiva i proactiva cap a l’aprenentatge i la formació continua, per a optimitzar les competències professionals i desenvolupar amb èxit l’activitat laboral, garantint una pràctica professional actualitzada i sensible a la realitat de cada persona. Què t’oferim?Incorporació immediata i vinculació laboral estable (contracte de substitució fins a cobertura definitiva de la plaça -antics interinatges-, segons RDL 32/2021)Jornada completa amb condicions regulades pel III Conveni SISCAT.Barems retribució (mínim-màxim): 51.440,90 - 67.705,47 euros bruts anuals.Formar part d’un equip compromès amb la qualitat assistencial i el servei públic.Entorn professional amb valors, equip multidisciplinari i projectes en evolució constant.Possibilitat de continuïtat mitjançant processos públics de selecció.*Pla de desenvolupament en matèria de competències lingüístiques en català en cas de no disposar del certificat requerit. O altres modalitats que en dret siguin possibles i que en cap cas seran de menor estabilitat que el contracte de substitució (com, per exemple, transitòriament un contracte de relleu previ al contracte de substitució, o un pacte de mobilitat vertical segons Codi de Selecció i Vinculació vigent). Procés de selecció:Les condicions generals d’aquesta convocatòria es regiran pel què recull el present anunci i amb els procediments que es detallen a les bases tipus de convocatòria per a ocupació de places vigents, que es poden consultar al web de l’entitat www.Tauli.Cat.Valoració Curricular: valoració del currículum vitae respecte la trajectòria professional, formació i l’expertesa vinculada a la posició segons allò exposat en els apartats anteriors (requisits i es valorarà).Entrevista personal o valoració directiva.Prova psicotècnica (si escau). Es podran afegir les proves competencials que es considerin necessàries per valorar la idoneïtat de les candidatures o en funció de la concurrència, en el marc de l’establert al vigent Codi de Selecció i Vinculació. En ares als principis d’economia processal i celeritat del procés, també es podran reduir les fases del procés de selecció en funció de la ràtio de candidats amb compliment dels requisits de la present oferta. Les persones no seleccionades per aquesta posició que hagin realitzat el procés de selecció, podran ser considerades, segons la seva idoneïtat, per ocupar vacants que es puguin donar en altres àmbits de característiques semblants a la plaça objecte d’aquesta convocatòria. En compliment de la LISMI, el Consorci, tindrà en consideració la reserva per a les persones candidates que acreditin una discapacitat igual o superior al 33%, sempre que siguin idònies per al desenvolupament de les funcions a cobrir. Vols participar-hi?En el moment de la inscripció a l’oferta de feina, cal adjuntar la següent documentació en format PDF:Currículum vitae.Titulació acreditativa requerida.(Opcional) Acreditacions formatives i certificats d’experiència laboral.La no presentació de la documentació requisit pot comportar l’exclusió de la candidatura a la convocatòria. Termini per presentar candidatura: fins a cobertura de necessitatsPer més informació: seleccio@tauli.cat (cal indicar el número de referència de l’anunci).Codi de plaça: 3275La no presentació de la documentació requisit pot comportar l’exclusió de la candidatura a la convocatòria.

El puesto consiste en la reparación, montaje y mantenimiento de utillajes y moldes, siguiendo los parámetros de calidad y procedimientos establecidos. Estas tareas son esenciales para garantizar la continuidad operativa y la eficiencia en los procesos de inyección. El rol implica una interacción constante con diferentes máquinas-herramienta y sistemas de control, asegurando que todo el equipo funcione de manera óptima y cumpla con los plazos de producción en Santa Perpètua de Mogoda. El profesional será responsable de utilizar equipos como CNC, rectificadoras, tornos, prensas y taladros para llevar a cabo el ajuste, reparación y mantenimiento tanto preventivo como correctivo de moldes y utillajes. Además, deberá gestionar eficazmente la información sobre el traspaso y la ubicación de los moldes mediante el software de control, manteniendo una trazabilidad completa. Una parte fundamental del trabajo consiste en revisar las órdenes de trabajo, cumplir con las especificaciones técnicas y actualizar los datos en las aplicaciones correspondientes para reflejar con precisión el estado de cada proyecto. El puesto exige una meticulosa atención al detalle y un profundo conocimiento técnico, ya que las actividades realizadas impactan directamente en la calidad del producto final y en la eficiencia de la línea de producción. Se requiere un enfoque proactivo para la resolución de problemas y la capacidad de trabajar de manera autónoma dentro de un entorno dinámico y orientado a resultados, siempre priorizando la seguridad y el cumplimiento de los estándares de la industria.

About the job Senior Mechanical Engineer Our client is seeking a Senior Mechanical Engineer to lead project teams in designing and developing mechanical system construction documents for healthcare building projects. This role encompasses overseeing the entire mechanical design process, ensuring alignment with project budgets, client goals, and multidisciplinary coordination. The ideal candidate will bring extensive experience in healthcare design, exceptional attention to detail, strong organizational skills, and effective communication abilities. This is an opportunity to make a meaningful impact on high-profile projects while fostering industry-leading practices and building lasting client relationships. KEY RESPONSIBILITIES: Perform technical design and quality control for assigned projects, including mechanical system calculations and layouts. Ensure adherence to best practices in engineering and compliance with current mechanical, energy, and FGI codes. Oversee the production of construction documents for new buildings, renovations, and facility additions. Conduct construction administration tasks, including site visits and shop drawing reviews. Identify and implement strategies to improve cost efficiency in designs. Mentor mechanical designers and assist with quality assurance reviews to maintain high standards. EDUCATION AND EXPERIENCE: Education: Bachelors Degree in Architectural or Mechanical Engineering from an ABET-accredited program. Experience: Minimum of 8 years in engineering, with a strong focus on mechanical systems. Proven experience designing healthcare building systems. Familiarity with mechanical, energy, and FGI codes. Medical gas design experience is preferred but not required. CERTIFICATIONS AND LICENSES: Fundamentals of Engineering (FE) certification (required). Professional Engineering (PE) license preferred but not required. Valid drivers license and willingness to use an insured personal vehicle for work-related tasks. SKILLS AND QUALIFICATIONS: Proficiency in Microsoft Office , Trane Trace , and Revit . Strong verbal and written communication skills. Exceptional organizational skills with meticulous attention to detail. Effective time management and multitasking abilities to meet deadlines. Team-oriented mindset with the ability to collaborate effectively. Legally authorized to work permanently in the country of employment without restrictions or sponsorship. WHY JOIN US? Our client fosters a culture of innovation, collaboration, and excellence, providing an opportunity to lead meaningful and impactful projects. The supportive and dynamic environment encourages career advancement and professional growth. Equal Opportunity Employer: Our client is committed to creating a diverse and inclusive workplace. They welcome applications from veterans and individuals with disabilities and provide reasonable accommodations to enable all qualified candidates to perform essential functions. If youre a skilled and motivated mechanical engineer ready to lead transformative projects, we encourage you to apply! #J-18808-Ljbffr

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know youve got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. Thats why we are always looking for curious minds that see themselves imagining the unimaginable with us. Your Role Investment Projects are where strategy meets execution, and this role sits right at that intersection. As an Investment Project Sourcing Manager within Technical Sourcing, you will lead end-to-end sourcing execution for complex technical investment projects across three global business sectors, primarily across sites in Spain and Italy with the flexibility to support projects across the broader EMEA region. Your work directly shapes the quality, cost, and delivery outcomes of strategic investments spanning architecture and engineering services, construction, and the installation of laboratory, infrastructure, and production equipment. You will serve as the critical link between internal stakeholders and the external supply base, translating business needs into sourcing strategies that maximize value through cost savings, risk reduction, and supplier performance. From early project involvement and procurement planning through supplier qualification, negotiation, contract management, and performance follow-up, you will own the full sourcing lifecycle with a focus on continuous improvement and cross-functional collaboration. Working across a diverse, international environment, you will build and maintain strong supplier relationships, resolve commercial disputes, and contribute to the evolution of category strategies by staying ahead of market trends and supply chain dynamics. If you bring a structured mindset, strong negotiation skills, and the drive to deliver results in a fast-moving global organization, this role offers real impact across the business. Who You Are Bachelor's degree in Business Administration, Engineering, or a related field, or an equivalent combination of education and relevant experience. Minimum 5 years of experience in procurement or engineering roles within multinational companies, with a preference for investment project sourcing in the chemical, pharmaceutical, or life science industry. Demonstrated ability to lead end-to-end sourcing processes including procurement planning, supplier qualification, competitive bidding, negotiation, and contract management for complex technical investment projects. Strong project management skills with the ability to work effectively in cross-functional and geographically diverse teams, managing multiple priorities in parallel. Experience identifying, managing, and mitigating supply chain risks, with the ability to anticipate market trends and translate them into actionable sourcing strategies. Excellent communication and stakeholder management skills, with the ability to engage and align across different seniority levels and functions in a complex global organization. Fluency in Spanish, Italian, and English (written and spoken) is required. Willingness and ability to travel up to 30%, primarily within EMEA. What we offer We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! #J-18808-Ljbffr

BOLD is expanding its engineering team to industrialise battery pack production lines, from prototype to small-volume production. You will define technical concepts, design layouts, and optimize processes for assembly, welding and EOL testing to ensure quality and manufacturability. You will collaborate with engineering to improve product designs for manufacturability, coordinate with suppliers and automation integrators, and drive continuous improvement from early development through ramp-up. #J-18808-Ljbffr

Liderar la estrategia y políticas de RRHH en una compañía industrial en crecimiento, gestionando la captación, desarrollo y compromiso del talento, así como las relaciones laborales y la cultura organizacional.

This job is with IMAN Group, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.

Salary Range: €69,100.00 - €128,300.00 Job Description Summary #LI-Hybrid Location: Barcelona, Spain This role is based in Barcelona, Spain. Novartis is unable to offer relocation support for this role. Please only apply if this location is accessible for you. The Regional PV QA Head provides end to end quality assurance vigilance expertise and support to global and local operational Pharmacovigilance (PV) and Device Vigilance activities within Novartis with a focus on the country organizations, as well as quality expertise in regional and local vigilance regulation, in order to ensure compliance with applicable regulatory requirements and Novartis procedures. Job Description Drive independently the regional and country quality oversight for implementation and maintenance of Novartis vigilance Quality Systems performed by the local teams, namely Quality Issue, proactive risk assessment and action management systems. Ensure, together with PS and PV in Countries and Regions team, that regional and country quality performance of the Novartis Vigilance System tasks and responsibilities is performed as required under global, regional and country PV regulations, to monitor that safety of the Novartis authorized products are met, and changes to their risk-benefit balance are identified. Support the regional and country Global Research and Development Quality management cycle through development, execution and accountability for deliverables of the global vigilance Quality Plan (QP). Coordinate execution of the QP with relevance to applicable regional and country patient safety activities and report the status to applicable Global PV QA team. Monitor indicators that relate to the performance, compliance and quality of regional and country vigilance systems, in line with indicators defined by Global PV QA team. Act as a quality champion by communicating risks to PS and PV and providing recommendations on potential mitigations. Promptly communicate regional and country compliance issues to Global PS&PV, PV QA management and QPPV. Proactively propose potential quality improvement measures and develop strategies aimed at simplifying processes and improving quality of outputs while ensuring compliance with regulatory requirements; share best practice within and across regions. Lead regional initiatives focused on quality improvement and compliance, provide ongoing project support and governance, as assigned. Provide expertise and support Global PV QA team in the execution of vigilance Quality Risk Assessments (QRA) to identify and mitigate regional and country PV risks. Support maintenance of the Novartis global Pharmacovigilance System Master File (PSMF), where applicable. Ensure a constant state of regional and country vigilance inspection readiness. In line with Global PV QA and PS&PV teams, prepare for, facilitate, provide expertise and lead logistics for Health Authority (HA) vigilance inspections, assess results of pre-inspection activities and HA inspection findings in terms of associated risks and communicate to management. Perform Quality check of vigilance inspection deliverables. Align with PS and PV team and review the inspection corrective and preventive (CAPA) plan, to ensure quality, consistency and appropriateness of commitments. Act as the functional QA approver of inspection CAPA plans from the PV inspections in country organizations in the QMS. Monitor the status of implementation of the CAPAs and approve the related evidence in the QMS, to ensure they are completed, appropriately documented and sustainable. Expertly guide the development of robust and sustainable CAPAs to address PV audit findings related to country organizations and act as functional QA approver of the CAPA plan in the QMS. Monitor the status of implementation of CAPAs to ensure they are completed, appropriately documented and sustainable and approve applicable related evidence in the QMS. Provide expertise and support country PS and PV and other business partners with identification and compliance of-Quality Issue investigations, act as functional QA in the QMS and ensure timely escalation of applicable Quality Issues to management; provide assistance in the remediation of PV system issues; ensure follow-up and monitoring of completeness of CAPAs in alignment with PV QA team. Oversee definition of PV self-assessment plans from Regional PS & PV team to regional and country pharmacovigilance processes as well as their execution. Review vigilance self-assessment reports and approve related action plans in the QMS. Identify regional and local training needs (for example via Quality Issues) and deliver knowledge sharing sessions that meet the needs of business and QA partners and improve overall quality and compliance of the Vigilance system. Provide guidance and recommendations on Merger & Acquisition as well as divestment relevant activities for integration or disintegration of the vigilance system, where applicable. Lead and/or support due diligence (DD) activities for potential product and/or company acquisitions, when applicable. Minimum Requirements Degree in Life Sciences or related scientific discipline. Higher degree desirable. Excellent written and verbal English communication skills; fluency in a second language a plus. Quality/ PV/ clinical/ regulatory affairs/ pharmaceutical industry/ health authority experience; GCP/PV/GMP auditing or inspection experience and Health Authority interactions a plus. Experience in PV in a country organization and global quality support to stakeholders in country organizations a plus. Ability to travel up to 20%. Ability to independently manage and objectively evaluate complex compliance issues with minimal supervision; Excellent problemsolving, decision making and prioritization skills. Quality mindset and excellent quality and compliance leadership and facilitation skills. Extensive knowledge of PV regulations, guidelines and policies; Awareness of GCP and Part 11 requirements. Ability to lead teams and operate successfully in various team capacities and diverse cultural environments. Ability to deputize for the Global Head PV QA Regions and Countries as needed. Benefits & Rewards At Novartis, we’re committed to reimagining medicine together - and rewarding the people that make it happen! Expected Annual Base Salary Range for role: 69,100.00 -128,300.00 EUR The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. Read our brochure to learn more about our global total rewards offering: Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. Skills Desired Business Acumen, Business Partnerships, Change Management, Communication, Continuous Improvement, Data Integrity, Digital Fluency, Ensure Compliance, GMP Operations, Good Laboratory Practices (GLPs), Good Manufacturing Practices (GMP), Leadership, Managing Ambiguity, Organizational Savvy, Problem Solving, Process Improvements, Quality Assurance (QA), Quality Compliance, Quality Management (QMS), Regulatory Compliance, Risk Management, Stakeholder Management, Storytelling, Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. #J-18808-Ljbffr

Inibsa, grupo farmacéutico con más de 75 años de experiencia, busca un QA Soporte GMP en Ingeniería para asegurar la correcta gestión y mantenimiento de la documentación técnica y GMP asociada a instalaciones y proyectos de ingeniería, mejoras continuas y soporte a auditorías de autoridades sanitarias. Entre tus responsabilidades estarán la elaboración y revisión de URS, FS, RA y validaciones, la gestión de P&ID y diagramas, la apertura de desviaciones y CAPA, y la colaboración estrecha con #J-18808-Ljbffr

We are seeking an experienced Senior Concrete Estimator with a deep understanding of self-performed, multi-story cast-in-place concrete structures in California. If you have 10+ years of estimating experience in this specialized field and excel at analyzing production rates, wed love to hear from you! Key Responsibilities: Perform detailed quantity take-offs and preliminary pricing for multi-story cast-in-place concrete structures in California. Accurately estimate man-hour production rates for various formwork systems, placing, and finishing tasks, leveraging historical data. Analyze and interpret project specifications, drawings, and construction documents to prepare precise cost estimates. Utilize estimating software, including Excel, Win Est, Cost-OS, Timberline Precision Estimating, Plan Swift, or On-Screen Takeoff (experience with Model-Based Estimating is a plus). Collaborate with project managers, engineers, and field teams to refine estimates and ensure alignment with project goals. Qualifications: Minimum 10 years of experience estimating self-performed cast-in-place concrete structures. Strong understanding of formwork systems, material costs, and labor efficiencies in concrete construction. Proficiency with estimating software tools; familiarity with Model-Based Estimating is a plus. Excellent analytical, communication, and organizational skills. What We Offer: We provide a comprehensive benefits package to support your well-being and professional growth: Medical Coverage Employer covers 100% of the employee's premium for Anthem Blue Cross PPO Platinum. Paid Time Off (PTO): 5 days PTO in Year 1 10 days PTO in Year 2+ (per Employee Manual) 3 Paid Sick Days 9 Paid Federal Holidays Bereavement Pay 401 K Retirement Plan If you're a detail-oriented estimator with a strong track record in multi-story concrete structures, we encourage you to apply! #J-18808-Ljbffr

Carglass busca un Solution Architect para unirse al equipo de Digital & IT en Mollet del Vallès. Diseñarás soluciones tecnológicas escalables y coherentes con la estrategia de la empresa, trabajando junto a Product Owners, desarrollo y DevOps para llevar ideas a implementación. Se requiere experiencia en .NET y arquitectura cloud, con nivel de inglés suficiente para entornos internacionales. Se valorará AWS/Azure, Agile y prácticas DevOps. #J-18808-Ljbffr

Boehringer Ingelheim GmbH is seeking a seasoned Solution Engineer to join its Salesforce Centre of Excellence. You will partner with IT and business teams to design, prototype, and deliver scalable Salesforce solutions, emphasizing low-code/no-code configuration, data integration, and customer-centr

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. Clinical trials are at the heart of bringing new therapies to patients — and the decisions made in early study design have a lasting impact on their success. As Solution Lead for the Study Design Platform, you will own the end-to-end delivery and continuous evolution of a next‑generation Software as a Service platform that enables smarter, data‑driven decisions in clinical study planning, protocol authoring, and scenario‑based operational feasibility analysis. You will join the Digital, Data & IT (DDIT) R&D team within our Healthcare sector, working at the intersection of clinical operations, digital innovation, and enterprise IT. During the implementation phase, you will act as the critical bridge between R&D business stakeholders, the IT team, and the software vendor. You will lead solution design activities, translate complex business requirements into clear functional specifications and process flows, support User Acceptance Testing (UAT), facilitate alignment workshops, and drive change management and user onboarding to ensure a successful platform rollout. Beyond go‑live, you will take ownership of lifecycle management: prioritizing enhancements, supporting releases, monitoring solution performance, and ensuring sustainable adoption and business value realization. Working across a global matrix organization, you will collaborate closely with R&D users, IT partners, and the software provider — and may also contribute your analytical expertise to broader digital R&D initiatives in the clinical trial space. This position is based in Spain, preferably Barcelona or Madrid, but other locations in Spain may also be considered. • You hold a Master's degree in life sciences, computer science, or a related field, or bring equivalent professional experience., • You have 5 or more years of experience as an IT Solution Lead, Application Lead, or in a comparable role within the healthcare or life sciences industry., • You bring in-depth knowledge of clinical trial processes, including protocol design, operational planning (country and site selection), and study conduct., • You have a proven track record of translating complex business needs into functional specifications and communicating effectively with both technical and non-technical stakeholders., • You have hands‑on experience contributing to IT solution delivery in regulated environments, with a solid understanding of software development lifecycles and computerized system validation (CSV) in line with GxP requirements., • You are familiar with clinical trial systems and clinical trial data standards, and can navigate a global matrix organization to build trusted relationships across R&D, IT, and external partners., • You are fluent in English (written and spoken) and bring a proactive, solution‑oriented mindset — you take ownership, anticipate challenges, and drive issues through to resolution. We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity! #J-18808-Ljbffr

Regulatory Affairs SpecialistApplyremote type: Not Remotelocations: Polinyà, Spain: MERU CEDEX, France: Gdansk, Poland: Poland: Pinneberg, Germanytime type: Full timeposted on: Posted 2 Days Agotime left to apply: End Date: July 29, 2026 (18 days left to apply)job requisition id: JR8439You Speak Up to Share Opportunities for Improvement and Drive Change? Would you like to thrive in a collaborative and professional work environment? If yes, come and join us!At Hempel, we work to shape a brighter future with sustainable coating solutions. Compliance, product stewardship, and responsible chemical management are essential to how we develop, manufacture, and market our products globally.We are looking for a Regulatory Affairs Specialist who is naturally curious about digital transformation initiatives, innovative ways of working and uses critical thinking to identify opportunities for process optimization, continuous improvement, and increased business value.Working within our Global Regulatory Affairs team, you will help shape more efficient, data-driven, and scalable regulatory processes while ensuring continued compliance with chemical regulations.This is a hybrid role based in Europe, with close collaboration across functions and regions.Do You Want to Work in an Environment Where Every Voice Is Valued and Respected? Are you excited by the opportunity to work on digital transformation key projects? If So, Keep Reading.Key task and Responsibilities Ensure compliance with EU chemical regulations (REACH, CLP, and related legislation) through effective regulatory stewardship, accurate data management, and robust compliance processes. Manage and maintain regulatory data in systems such as Chemmate, IUCLID, and other digital platforms, while developing and enhancing reports, dashboards, and tracking tools using Excel, Power BI, SQL, and internal Regulatory Affairs systems. Apply critical thinking to conduct regulatory assessments and support product development, reformulation, and change management activities, translating regulatory requirements into practical business solutions. Evaluate existing Regulatory Affairs processes and identify opportunities to improve efficiency, data quality, and user experience through digital tools, automation, and streamlined ways of working.* Collaborate with stakeholders across regions to harmonize regulatory practices, support the digital transformation of Regulatory Affairs, and represent Hempel in relevant industry associations.Do You Dream of Working in a Culture of Inclusion, Transparency, and Support? Here’s what it takes to become our next team member. A university degree in Chemistry, Chemical Engineering, Data-related Scientific Fields, or a similar discipline, combined with experience working with digital regulatory systems, databases, spreadsheets, and reporting tools. Experience in Regulatory Affairs within the chemicals, coatings, or manufacturing industry, with the ability to translate regulatory requirements into practical and effective business processes. Solid knowledge of European chemical legislation, particularly EU REACH, CLP, and product stewardship, coupled with a proactive and solution-oriented approach to regulatory challenges. Advanced skills in Excel (including structured data management, pivot tables, and formulas); experience with Power BI, Chemmate, IUCLID, SQL, or similar digital and reporting tools is a strong advantage. Strong analytical and critical-thinking skills, with a continuous improvement mindset and an interest in leveraging digital solutions to enhance efficiency, data quality, and business value. Fluency in English; additional European languages are an advantageSounds like a match?Welcome to apply! Click the ‘Apply for position’ button in the top-right corner and submit your application letter with a CV in English via our recruitment system.Application due Seniority LevelAssociateJob FunctionsInformation Technology, LegalIndustryChemicalsAt Hempel, you’re welcomed to a global community of +7000 colleagues around the world. A workplace built on shared trust, mutual respect and support for each other. We’re on a mission to double our impact. To succeed, we need bright minds and team players. Which is why, from day one, your input, ideas and initiative are not only welcomed, but expected. In return, you will enjoy great opportunities for development in a growing global company – and be part of the solution by contributing to our global impact. At Hempel, we are committed to everyone feeling safe, valued and treated equally, in an environment where each employee can bring their authentic selves to work. We believe that inclusion is key to innovation and by bringing together the most diverse perspectives and talents, we can achieve great things, together. #J-18808-Ljbffr

Diseñador/a de Utillaje (Tooling Design) Que harás Diseño e Implementación de Utillaje Trabajar estrechamente con el equipo de taller para identificar desafíos en el proceso de fabricación y comprender los requisitos del utillaje con el objetivo de mejorar la eficiencia. Diseñar y desarrollar utillajes utilizando software CAD (ej. Catia 3DX), iterando en función del feedback real del área de producción para asegurar que las soluciones estén alineadas con las especificaciones del proyecto y sus necesidades. Realizar estudios de viabilidad y validaciones antes de la implementación para garantizar que las herramientas cumplen con los estándares de seguridad, ergonomía y funcionalidad. Crear prototipos iniciales y bocetos de conceptos de utillaje, asegurando que cumplan con los requisitos técnicos y de fabricación. Realizar pruebas funcionales para garantizar la usabilidad, durabilidad y seguridad de las herramientas antes de su implementación. Participar activamente en el ensamblaje e instalación de nuevas herramientas en planta para validar su rendimiento y ajustar diseños si es necesario. Generar documentación técnica detallada, incluyendo planos, tolerancias y especificaciones para fabricación. Colaborar con el equipo de compras y proveedores para resolver dudas y problemáticas en relación con los requisitos de utillaje y materiales. Formación y Experiencia Ciclo formativo de grado superior en Diseño Mecánico, Ingeniería de Fabricación o un campo relacionado. Se valora experiencia práctica en un entorno de taller o fabricación. Experiencia en diseño mecánico, fabricación de herramientas o desarrollo de utillaje. Habilidades Dominio de software CAD (ej. Catia 3DX, SolidWorks). Conocimiento de GD&T (Geometric Dimensioning & Tolerancing). Familiaridad con procesos de fabricación, materiales y sistemas mecánicos. Conocimientos básicos de ergonomía y requisitos de seguridad en el diseño de herramientas. Mentalidad resolutiva con un enfoque práctico. Sólidas habilidades de colaboración y comunicación para trabajar con distintos equipos. Capacidad para gestionar múltiples proyectos y priorizar tareas de manera efectiva. Beneficios Compensación competitiva. Seguro de vida. Seguro médico privado con coste reducido para empleados y familiares. Comedor subvencionado. Horario flexible y hasta 5 días de teletrabajo al mes. #J-18808-Ljbffr

INDIBA seeks a Group Finance Specialist / Senior Finance Manager to join the Finance team in Sant Quirze del Vallès (Barcelona). Reporting to the Group Controller and working closely with the CFO, this role supports the group across accounting, audit, consolidation, tax, treasury and finance projects. The candidate should be a senior finance problem solver with a strong technical background, capable of analyzing complex matters and providing practical recommendations for international expansion. #J-18808-Ljbffr