Trabajos delivery en Lliçà De VallCrear alertas

Substantial experience in IT project management (+8 years), program delivery, or application delivery in complex environments. Familiarity with Agile and traditional delivery approaches. Business fluency in English, written and spoken, and the ability to travel regularly, including regional and inte

Play a pivotal role in bringing the new ONE Deco vision to life by orchestrating global projects such as product innovation and optimizing operational processes. As a Global Program Manager within ONE Deco, you’ll drive innovation and excellence in product development and operational processes across all brands in the decorative segment. • Act as portfolio manager for assigned Decorative Segment annual strategic projects., • Orchestrate One Deco strategic projects encompassing cross‑brand and cross‑functional elements., • Lead and update the One Deco segment product pipeline., • Handle Segment Innovation and Sustainability projects, ensuring a powerful, innovative, and sustainable global Deco pipeline (PaintGreen) roll‑out and anchor Segment Product Development governance and operations (ColourGate) Supply to Rethink Innovation and delivery of differentiated solutions., • Harmonize segment product management community and follow‑ups., • Ensure annual project results and long‑term strategic progress with a focus on innovation, sustainability, and operational excellence initiatives., • Top‑tier project manager with cross‑functional project experience and a consistent record of success., • Broad understanding of company processes and stakeholders; solid knowledge of technical products and operational execution., • Global, collaborative attitude with fluency in English and excellent partner and interpersonal skills., • Experience coordinating across functions, geographies, and cultures, and ability to take action with flexibility and creativity across many time zones., • Strong influencing skills and a global mindset., • Ability to work independently and as part of a close‑knit team. At Hempel, we are committed to promoting a workplace that celebrates and values unique backgrounds, perspectives, and talents. We provide training and initiatives to support an inclusive culture, ensuring every employee feels respected and empowered to bring their authentic selves to work. Senior Level: Senior Level Interested in applying? Submit your application letter with a CV in English via our recruitment system. #J-18808-Ljbffr

Why join theSourcingdepartment? At the heart of every project, ourSourcing teamsdevelop innovative strategies for the procurement of materials and services, ensuring high-quality partnerships and effective cost management. We are committed to deliveringsustainable solutionsthat meet environmental requirements while achievingbest-in-class performancein our industry. By joining our Sourcing team, you will play a key role inselecting the best suppliersandoptimizing our supply chain. You will work within a passionate team dedicated to findinginnovative and sustainable solutionsto meet the challenges of a constantly evolving sector. Within the Sourcing department, we are shaping theelectrical world of tomorrow. Join us and be part of the journey! As a Country Purchaser Regional Sourcing (m/f/d) you will report to Regional Sourcing Managerin theSourcing departmentbased inLa Roca del Vallesfor aPermanentcontract. The role of Country Purchaser is to manage country specific purchasing topics to support regional business development. To do so the jobholder drives regional execution and supply continuity aligned with global strategies and regional business needs, facilitating Hager global sourcing footprint. Duties & Responsibilities • Being accountable to manage a defined group of vendors and partnerships in order to reach Hager objectives regarding quality, costs, lead time, compliance and sustainable criteria to ensure the application of concerned sourcing strategy. To do so she/he leads the commercial negotiations., • Incorporate environmental, social and corporate governance (ESG) requirements as part of the sourcing and ensures that vendors and any other business partners are matching Hager objectives set in the Code of Sustainable Sourcing., • Develop and manage overall regional sourcing roadmaps and strategies for assigned spend categories aligned with group sourcing policy and strategies and oversee the execution of initiatives. Be accountable for reporting of sourcing savings and compliance., • Promote collaboration between Hager’s Category Management to find synergies and unlock additional sourcing opportunities and negotiate aggregated volumes to achieve commercial benefits., • Ensure deployment of category strategies in the regions., • Drive a high-level performance within a culture of collaboration, whilst focusing on process standardization, implementation of best in class practices., • Drive the implementation and regional rollout of the “No PO, No Pay” group initiative, ensuring local stakeholder alignment and compliance and provide required deliverables in time., • Establishing and maintaining a supplier base that effectively safeguards the company against financial and operational risks. This includes the development and implementation of action plans for identified risk suppliers. In addition, the position ensures full compliance with the Group Purchasing Policy throughout all relevant processes. Qualifications & Requirements • Academic degree or relevant commercial/technical education., • A minimum of 5 years’ experience of purchasing and procurement techniques., • Proven track record of delivery of value from strategic activities., • Operationally und technical savvy and having the ability to effectively manage projects simultaneously whilst meeting agreed deadlines and goals., • Demonstrated ability to navigate and collaborate across functions, businesses, geographies and disciplines., • Strong presence and interpersonal skills, with the drive to build effective partnerships with key internal stakeholders, vendors and other business partners., • Proven negotiation skills up to senior management level with understanding of contractual negotiation, development, and local regulations., • Fluent proficiency in English, Spanish and Catalan. What we offer? • Personalized onboarding experience programdesigned to make your first dayssmooth, • Opportunities to learn and grow through Hager Group's awarded HiUniversity., • Internal career opportunities, over 25% of our recruitments are through internal mobility What are the recruitment stages? • Once your CV has been selected, you will be contacted by a recruiter for an initial phone exchange., • You will be invited for a first interview with the hiring manager & the recruiter, • A second Interview will be then organized with the N+2 & the HR manager Our success relies on collective energy. Apply now and power up your future with us! #J-18808-Ljbffr

Merck Healthcare seeks an IT Solution Lead for the Study Design Platform to own end-to-end delivery of a next-generation SaaS solution enabling smarter, data-driven clinical study planning and protocol authoring.

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). 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. • 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., • 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. • 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

Volpak is a leading organization headquartered in Santa Perpétua de Mogoda, Spain. As a key player in pouch‑type packaging for over 40 years, we specialize in designing horizontal form‑fill‑seal, vertical multi‑lane, and cartoning machines. Our business portfolio encompasses a wide range of innovative solutions in consumer goods products, such as sauces & condiments, dairy, and confectionery, while extending its capabilities to meet the needs of other sectors like pet food, home care and chemicals. We strive to continuously expand our offerings and enhance our capabilities to meet the evolving needs of our customers. For more detailed information about Volpak and its comprehensive business landscape, please visit Volpak is part of Coesia, a group of innovation‑based industrial and packaging solutions companies operating globally, headquartered in Bologna, Italy. Coesia operates in 36 countries with 20 different companies and employs over 8,000 people as of 2023. About the Role: We are looking for an Assembly Process Engineer to join our Operations team. In this role, you will ensure continuous improvement of machinery assembly performance by applying Lean Manufacturing standards and acting as a change agent to promote Lean Six Sigma methodologies across the organization. You will work cross‑functionally with Engineering, Operations and Quality, helping translate technical solutions into efficient, standardized assembly practices that improve performance, reliability, and delivery. As Assembly Process Engineer , you will: • Drive continuous improvement of existing machine features to enhance performance, durability and reliability—aligned with cost, timing, quality standards, technical requirements and defined KPIs., • Design dedicated assembly tooling to improve efficiency, quality, ergonomics and repeatability., • Lead and participate in kick‑off and closing meetings for assembly projects, collecting and analyzing end‑to‑end assembly process data to identify improvements., • Transfer technical information from the Engineering department to all stakeholders involved in assembly activities, ensuring clarity and alignment., • Convert production know‑how into standards (Standard Work): procedures, rules, norms, and best practices., • Ensure correct configuration of devices, machines, and groups, minimizing inventory obsolescence. What You Need to Be Successful: • Engineering degree (Mechanical, Industrial, Electrical, or equivalent)., • 2-3 years of experience in a similar role., • Proven experience as a Process Engineer in a manufacturing environment applying Lean principles and methodologies (e.g., production BOM, lean cell design, standard work definition, 5S)., • Knowledge of 3D CAD software (SolidWorks and Composer)., • Strong analytical capability to collect, structure and interpret data to define improvement strategies., • Proficiency with MS Office tools (Word, Excel)., • Knowledge of SAP, • Good command of English and Spanish ., • Availability to travel worldwide when required., • Ability to manage multiple and complex processes with accuracy and attention to detail., • Team‑oriented, results‑driven and comfortable working with deadlines., • Innovative, proactive approach and strong understanding of customer needs. Coesia is an equal opportunity employer. We believe in fair, merit-based recruitment and assess all candidates exclusively on the basis of their qualifications, skills, experience and suitability for the role #J-18808-Ljbffr

Merck Group in Spain seeks an Analytics Architect within the Enabling Functions Data Office to design and deliver high-impact data and AI solutions that power smarter ways of working across the organization. You will join a collaborative, internationally distributed team delivering data products at scale in a Product-Oriented Delivery model. You will work with Snowflake, AWS, Palantir Foundry and end-to-end data pipelines, focusing on governance, security, and regulatory compliance while #J-18808-Ljbffr

Masterdata Application SpecialistApplylocations: Granollers Officetime type: Full timeposted on: Posted Yesterdayjob requisition id: JR ## Job PurposeThe Master Data Management Specialist plays a critical role in ensuring the accuracy, consistency, governance, and lifecycle management of master data across Audens Food, with an extended scope supporting the wider GoodLife Foods Group. Acting as the key link between business stakeholders and IT, the role ensures that high-quality master data supports operational excellence, strategic initiatives, and business transformation.This position is responsible for maintaining a reliable single source of truth for Product, Customer, Supplier, and other critical business data, enabling efficient operations, regulatory compliance, and informed decision-making across the organization. The role also contributes to the successful delivery of system implementations, data integrations, and continuous improvement initiatives aimed at strengthening data governance and business processes.## Key Responsibilities* Manage and oversee the day-to-day maintenance of master data within Synergy MDM and connected enterprise systems, ensuring data integrity and operational continuity. Ensure master data is accurate, complete, and compliant with established governance policies, business standards, and quality requirements. Serve as the subject matter expert for master data management processes, supporting data quality initiatives and promoting best practices across the organization. Lead the master data workstream in ERP implementations, system integrations, data migrations, and business transformation projects. Support and coordinate integrations between Synergy MDM, ERP systems, GS1 data exchanges, APIs, and EDI interfaces to ensure seamless data flow across business applications. Collaborate closely with cross-functional stakeholders to identify, investigate, and resolve data quality issues while implementing sustainable corrective actions. Develop, maintain, and continuously improve master data documentation, governance standards, operating procedures, and user training materials.* Drive continuous improvement initiatives focused on enhancing master data processes, governance frameworks, controls, and overall data quality.## Key StakeholdersThe role requires close collaboration with a broad range of internal and external stakeholders to ensure effective master data governance and support business operations.Internal stakeholders IT Enterprise Application Manager Master Data Management Team Sales Operations Supply Chain Finance Procurement Quality Assurance* ERP and Application Support TeamsExternal stakeholders Software vendors System implementation partners* GS1 and other external data exchange partners## Role Dimensions* Preferred location: Granollers, Spain* Business scope: Multiple manufacturing sites across Audens Food and GoodLife Foods* Core systems: Synergy MDM, Izaro ERP, and other connected enterprise applications* Master data portfolio: + Approximately 1,000 product articles and 2,000 product items + Approximately 700 customer records + Approximately 3,500 supplier records* Travel: Occasional travel within Spain and to Breda, The Netherlands## Qualifications & Experience Bachelor's degree or equivalent professional experience. Minimum of 2–3 years' experience in Master Data Management, ERP systems, or enterprise business applications. Previous experience within manufacturing, FMCG, food production, or supply chain environments is highly desirable. Strong understanding of data governance principles, master data management processes, and data quality frameworks. Good knowledge of Microsoft 365 applications and basic relational database concepts. Experience working with ERP systems, APIs, EDI integrations, and GS1 data standards.* Fluent in both Spanish and English, with excellent written and verbal communication skills.* Willingness to travel occasionally as required.## Key CompetenciesThe successful candidate combines strong technical expertise with excellent analytical and interpersonal skills, enabling effective collaboration across business functions while ensuring high standards of data quality.Core competencies include: Strong analytical thinking and problem-solving capabilities. Exceptional attention to detail and commitment to data accuracy. Advanced Microsoft Excel skills, including formulas, Pivot Tables, VLOOKUP/XLOOKUP, conditional formatting, data validation, data comparison, transformation, and preparation of bulk upload files. Excellent stakeholder management and communication skills, with the ability to collaborate effectively across technical and business teams. Ability to work independently, prioritize competing demands, and manage multiple projects simultaneously. Project-oriented mindset with experience supporting business transformation and change initiatives. Proactive, pragmatic, and continuous improvement approach. Ability to translate business requirements into practical data management and system solutions that support organizational objectives.At GoodLife Foods we believe that great food brings people together and makes every moment more enjoyable. With a team of over 1,700 professionals across Europe, we are leading the way in frozen snacks and offer a diverse range of irresistible food - each made with care, expertise, and the finest ingredients. Behind all our products are great people. As we continue to grow our business, we’re building the foundation for one GoodLife Foods: a place where teams connect, processes align and our collective strengths come together. Working at GoodLife Foods means joining an organisation where diverse cultures and perspectives are celebrated while fostering one unified organisation. We strive to ensure everyone feels valued and connected. #J-18808-Ljbffr

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well‑being of people around the world. We are leaders in plasma‑derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding. The IT Validation Technician actively contributes to the execution of the defined validation methodologies which comply with company standards and regulatory requirements. This role also oversees teams and validation resources engaged in validation activities. • Relationship Management, Planning, and Strategic Alignment, • Builds effective and trusting working relationships with all business and IT partners in areas of responsibility and collaboration., • Continuously improves knowledge of business processes, industry trends, and IT systems to better communicate IT capabilities and support IT solutions development., • Project Delivery and Management, • Proactively identifies project risks and issues, helps determine necessary escalation, mitigation, and resolution steps., • Regularly communicates deliverables status, concerns, and issues to direct Manager, the Project Manager, and the project team., • Participates in estimating project cost and time requirements, assessing capabilities and support/resource requirements in area of responsibility., • Creates, reviews, updates, and may approve CSV documentation for changes and projects as assigned in accordance with IT Methodology: Validation Plans, Risk Analysis, Validation Test Designs and Reports., • Assures the compliance of the GxP relevant IT systems with the regulatory and data integrity requirements., • IT Operational Support, • Ensures IT quality and regulatory compliance through adherence to quality control standards in all activities., • Contributes to the development, documentation, and evolution of IT policies, procedures, and tools to align with business and IT strategies and ensure sustainability of services, • Regularly communicates individual task status, open issues, and challenges to impacted stakeholders and/or direct manager., • Knowledge Sharing and Consulting, • Participates in the education of partners in industry and IT best practices in areas of responsibility and expertise., • Mentors peers and junior level staff with both challenging and routine assignments by sharing knowledge and experience., • Shares developing expertise of industry and IT best practices with peers and business partners., • May participate in the development of ongoing training for IT staff in specific areas of knowledge., • Provides support in the event of internal and external audits of validated systems, preparing supporting documentation as required., • Participates in the continuous enhancement of systems, technologies, methodologies, and services to improve IT effectiveness and system performance. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. • Bachelor’s degree in Life Sciences (Biology, Pharmacy, Biotechnology, Chemical or a related discipline)., • Minimum of 3 years of proven experience working within a regulated pharmaceutical environment, including GxP compliance., • Solid understanding of project management methodologies, tools, and best practices., • Knowledge of regulatory requirements and GxP standards applicable to computerized systems., • Experience supporting regulatory inspections and audit responses., • Strong attention to detail with the ability to manage multiple priorities simultaneously., • Ability to work both independently and collaboratively in cross‑functional and international teams., • Excellent organizational, communication, and problem‑solving skills., • Advanced in English, with the ability to work effectively in an international environment., • Flexibility for U Program: Hybrid Model., • Contract of Employment: Permanent position. Grifols is an equal opportunity employer. #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 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

What would you do? 1. Strategic Account Governance & Executive Communication Serve as the primary point of contact and trusted advisor for executive, operational, and technical stakeholders. Facilitate regular executive touchpoints, leading Quarterly Business Reviews (QBRs), Executive Business Reviews (EBRs), and Monthly/Quarterly Steering Committees (Steer Cos) with VPs and C-Level leaders to align on strategy and business outcomes. Oversee regular alignment meetings to monitor short-term action plans, track deliverables, and manage engagement across regional and leadership teams. Translate technical capabilities and operational data into compelling executive stories that demonstrate clear business value and ROI. 2. Business Growth, Strategy & Change Management Develop and execute long-term, multi-threaded account strategies and Success Plans aligned with each customer's digital maturity and business objectives. Assess client digital maturity to build tailored operational roadmaps that drive e-commerce performance using Instaleap’s capabilities. Drive organizational change management to help client HQ and leadership teams adopt digital transformation initiatives. Identify process optimizations, conversion improvements, and last-mile/fulfillment performance gains. 3. Commercial Partnership & Account Expansion Uncover account expansion opportunities by introducing new workflows, best practices, and additional Instaleap solutions. Partner closely with the Sales/Account Executive team on upsell and cross-sell initiatives. Lead business value conversations during commercial discussions. Represent Instaleap at key industry commercial events (e.G., Shop Talk, NRF Retail's Big Show Europe, Euro Shop, e Commerce Expos). 4. Operational Alignment & Data-Driven Consulting (In collaboration with the Customer Operations Analyst supporting the account) Analyze key performance metrics (e.G., order fulfillment rate, delivery time, OTIF, conversion rates) alongside the Customer Operations Analyst to extract actionable insights and assign client-side ownership. Oversee the implementation of customized dashboards and reports to track success indicators across various stores, regions, and timeframes. Conduct root-cause analysis when performance deviates from targets and execute cross-functional correction plans. 5. Client Onboarding, Enablement & Advocacy (In collaboration with the Customer Operations Analyst supporting the account) Direct structured onboarding programs, training sessions, and knowledge transfers for client HQ and operational teams, supported by the Customer Operations Analyst. Ensure the ongoing maintenance of client-specific documentation, playbooks, and operational best practices. Act as the internal voice of the customer, escalating client priorities and feeding real-world operational insights into Instaleap's Product, Technical, and Support roadmaps. 6. Risk Management & Health Monitoring Track early risk indicators (e.G., declining platform usage, delayed rollouts, missed KPIs) and build proactive mitigation plans. Lead cross-functional resolution efforts during escalations to protect account health. Your experience has been shaped by 6+ years of experience in Enterprise Customer Success, Strategic Account Management, Enterprise Saa S, or Top-Tier Management Consulting. Proven track record managing Large Enterprise / Strategic Accounts ($1 M+ ARR / complex retail accounts) with C-suite and VP stakeholder mapping. Strong commercial awareness and demonstrated capability to identify account growth/expansion opportunities. Experience leading executive presentations and high-stakes business reviews. Cross-functional collaboration experience with Product, Engineering, Sales, and Support teams. Language Requirements English: Professional / Native Proficiency (Required). Preferred (Nice to Have) Spanish OR Portuguese: Professional Proficiency (Highly Preferred). Direct domain experience in Grocery, Retail, E-commerce, Last-Mile, or Logistics. Prior experience managing European/UK enterprise customers. Familiarity with enterprise CRM/Ecommerce systems (Salesforce, Hub Spot). Your Super Powers Customer Success & Value Realization Strategic Account Management & Multi-threading Consultative Selling & Commercial Mindset Executive Presence & Storytelling Change Management & Conflict Resolution Data Analysis & Risk Mitigation Language Requirements: English Professional / Native Proficiency (Required). Preferred (Nice to Have): Spanish OR Portuguese: Professional Proficiency (Highly Preferred). Direct domain experience in Grocery, Retail, E-commerce, Last-Mile, or Logistics. Prior experience managing European/UK enterprise customers. Familiarity with enterprise CRM/Ecommerce systems (Salesforce, Hub Spot). What we bring to the table Indefinite-term employment contract under Spain labor law. Health insurance: Prepaid medicine. Monthly activities with your team. #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

Evonik in Spain is seeking a senior project manager to lead cross‑functional chemistry and nanotechnology initiatives. You will coordinate applied innovation, regulatory, engineering and manufacturing teams to ensure on‑time, on‑budget delivery of complex projects. You’ll drive risk management, reporting to senior leadership, and foster international collaboration in a hybrid work environment that supports professional growth within a global science and engineering company. #J-18808-Ljbffr

Manages and coordinates the complete artwork lifecycle for product packaging and labels, ensuring accuracy, compliance, and timely delivery through cross-functional collaboration.

Volpak, part of Coesia, is seeking an Assembly Process Engineer to join our Operations team in Santa Perpétua de Mogoda, Spain. The role focuses on continuous improvement of machinery assembly using Lean and Lean Six Sigma methodologies to raise performance, reliability and delivery. You will work cross-functionally with Engineering, Operations and Quality to translate technical solutions into standardized assembly practices, design tooling, lead project kick-offs, and convert production #J-18808-Ljbffr

Grifols, S.A. is seeking a Manufacturing Engineer (Equipments & Installations) to lead the design, installation and qualification of new manufacturing equipment and facilities. You will work closely with Manufacturing, Quality, Validation and Maintenance to ensure GMP compliance and timely delivery of projects. The role requires coordinating external engineering firms, suppliers and contractors, overseeing construction, and driving improvements in utilities and production areas. #J-18808-Ljbffr

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

Merck Group in Spain and Italy seeks an Investment Project Sourcing Manager within Technical Sourcing to lead end-to-end sourcing for complex technical investment projects across three global sectors, spanning architecture, engineering, construction, and lab equipment. You’ll align internal stakeholders with suppliers to optimize cost, quality, and delivery in a fast-moving, international setting. Fluency in Spanish, Italian, and English, 5+ years in multinational procurement or engineering, and #J-18808-Ljbffr

Se solicita personal de Repartidor/a autónomo/a con furgoneta propia.Por favor, verifique que tiene el nivel de experiencia y las cualificaciones adecuadas leyendo la descripción completa de esta oportunidad a continuación.Ubicació: BARCELONA - VALLÈS OCCIDENTAL - 08184 PALAU-SOLITA I PLEGAMANS

Merck Group in Spain seeks an experienced IT Project Manager to drive application projects that optimize Supply Chain planning, manufacturing, and logistics.Si está considerando enviar una solicitud, asegúrese de pulsar el botón de solicitar de abajo después de leer la descripción completa.You

Go Delivery Phama busca repartidor/a autónomo/a con furgoneta propia para distribuir pedidos a farmacias en la zona de Palau-solità i Plegamans y alrededores.

Substantial experience in IT project management (+8 years), program delivery, or application delivery in complex environments. Working with business owners, IT colleagues, architects, vendors, and stakeholders across functions and regions, you will lead delivery from initiation through transition to

Excellent stakeholder management and communication skills, with the ability to influence without direct authority across business and IT teams. Pragmatic, structured and delivery-oriented, with the ability to balance governance discipline with business agility. It is a brilliant opportunity for you,

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

As marketing moves into a new functional structure, this role becomes the connective layer that turns strategy into disciplined, on-time delivery: taking work from intake through planning, execution, and launch, with clear ownership and visibility at every step. Break marketing initiatives (campaign

Roche invites a seasoned professional to join as Product Operations Lead (POL) within Roche Informatics (RIS) in Sant Cugat del Vallès.You will bridge strategy and execution across Life Cycle, ensure a single source of truth for investments and capacity, and enable operating model adoption while re

Jones Lang LaSalle Incorporated in Madrid (Remote) is seeking a Property Delivery & Facilities Manager to oversee a European industrial portfolio.

BSI is seeking an experienced Senior Operations Manager to lead our Continental Europe and META core delivery teams from a home-based role across the EMEA region. In this leadership position you will partner with regional stakeholders, harmonize processes, and ensure compliant, scalable delivery tha

GT Motive seeks a seasoned Product Owner to lead delivery of project value by aligning stakeholder objectives with cross-functional collaboration, ensuring timely, cost-efficient, and well-structured execution.

We are looking for an experienced and data-drivenSenior Program Manager – Platform Deliveryto lead the software delivery operations of our data, analytics, AI & integration platforms teams. You will champion continuous process improvement, agile best practices, and KPI-driven delivery to ensure ou

This fully remote role oversees governance, budgets, roadmaps, and delivery across engineering, QA, cybersecurity, and compliance teams, partnering with executives to balance innovation with regulatory obligations. You will guide PMOs, implement scalable delivery practices, manage risks, and report

You will monitor delivery, language quality, and adherence to client requirements while collaborating with Language Services to meet capacity needs and quality targets.

Appen is seeking a hands-on GenAI Project Delivery professional to orchestrate annotation, QA, and data collection for frontier models in Spain. You will ensure task configuration, contributor performance, and data quality align with client expectations while improving delivery standards at scale.

Delivery Lead to oversee the production and delivery of congresses, meetings and brand experiences for a key pharmaceutical client. You will mentor Project Managers, optimize delivery processes and collaborate with the Account Lead to sustain client satisfaction and performance.

Heymondo, a rapidly growing travel insurance company, seeks a Digital Portfolio Analyst to act as a servant leader within the software delivery team. You will aid backlog planning, roadmap design, and cross-functional coordination with Product Managers, QA, and IT to ensure timely delivery.

You will drive accurate, compliant, and timely payroll delivery while partnering with HR, Finance, and external vendors.

We are looking for an experienced, passionate Operations Delivery Leader to lead our core delivery operations in Continental Europe (CE) and the Middle East, Türkiye & Africa (META). As our Operations Delivery Leader, you will provide strategic and operational leadership to the CE & META core deliv

Boehringer Ingelheim GmbH in Spain seeks an experienced Senior Program Manager – Platform Delivery to lead software delivery operations for data, analytics, AI & integration platforms. You will champion continuous process improvement, agile best practices, and KPI-driven delivery to ensure platfor

Glovo is part of the Delivery Hero Group, the world’s pioneering local delivery platform, our mission is to deliver an amazing experience - fast, easy, and to your door. Delivery Hero has been listed on the Frankfurt Stock Exchange since 2017 and is part of the MDAX stock market index.

Own the technical delivery of your assigned system.

You will conduct ongoing customer interviews, market trend analysis, and competitive reviews, drive cross‑domain delivery with Engineering and PMO, and ensure GTM readiness across departments on a.

La persona trabajará en IT Operations/Service Delivery, con un mínimo de 3 años de experiencia y nivel alto de inglés.

As our new European Payroll Service Delivery Manager, you will ensure the successful delivery of payroll services across Europe, acting as the primary interface between Ramboll, payroll vendors and their local subcontractors, HR, Finance, ICT, and other key stakeholders. European Payroll Service Del