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Amaris is looking for a Data Manager with strong experience in clinical data management for CRO environments. The position focuses on supervising data management activities to ensure the smooth progress and quality of clinical projects. 🔥 Your Responsibilities • Act as the main point of contact for all data management topics and participate in project/study meetings, • Contribute to the selection of subcontractors by preparing specifications and evaluating proposals, • Participate in study design, including data management sections in protocols and CRF specifications, • Oversee outsourced data management activities, ensuring compliance with cost, timelines, and data quality, • Validate deliverables such as data management plans, validation plans, transfer specifications, eCRF completion guides, and coding instructions, • Test eCRF before production deployment and after each protocol amendment, • Implement targeted quality control of data based on risk assessment, • Monitor progress of data management steps (entry, cleaning, coding, external data transfers, SAE reconciliation, etc.), • Approve SDTM specifications and verify SDTM packages as needed, • Regularly assess subcontractor service quality, establish action plans for deviations, and discuss corrective measures, • Participate in data review meetings and validate associated reports, • Ensure responsibility for database lock and unlock, verifying all prerequisites, • Provide statisticians with data for statistical analysis, • Verify the presence of all data management documentation in the Trial Master File (TMF) 🎯 Your Qualifications • Experience in clinical data management for CROs (5–10 years), • Proficiency with industry-standard data management tools and software, • Academic background in Life Sciences, Pharmacy, or related field, • English fluent. French is a plus., • You demonstrate strong analytical and problem-solving skills, • You demonstrate excellent communication skills 💡 What You’ll Get From Us • An international community bringing together 110+ different nationalities, • An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities, • A robust training system with our internal Academy and 250+ available modules, • A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.), • At Mantu, sustainability is part of everything we do. You’ll have the opportunity to turn your ideas into action and make a tangible impact. Every day, our teams bring our ESG commitments to life, from reducing our footprint to driving positive change within our communities. Through our WeCare Together program, you’ll be empowered to design and lead projects that create real social or environmental impact, with the company’s full support. Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

Descripción del puesto Como Project Manager para proyectos recurrentes en Compoxi, serás responsable de coordinar y gestionar los proyectos asignados desde inicio a fin, de nuestro sector aeroespacial y aeronáutico. Pensamos en una persona que sepa aplicar las disciplinas de un jefe de proyecto, asegurando que se cumplan los objetivos establecidos de costos-presupuesto, tiempo, entregas y calidad. Reporte a: Managing Director Responsibilities - Project control: The Project Manager has the last responsibility of all matters occurring within their project. This covers all events from all types. Most common are listed below Scope: Project manager is responsible to understand the requirements from the client and to transfer them inside Compoxi, ensuring that the requirements have been clearly understood and tracked internally. Planning: Project Manager is the last responsible from the planning of the project. Project manager creates, updates and tracks planning of the project and request resources to accomplish the project scope. Cost: The project manager receive a close budget from commercial department and ensures that activities are executed according to the cost budget. Project manager tracks the cost expenditures and proposes cost savings opportunities and countermeasures to cost deviations Quality: Project Manager derives quality requirements to the quality requirements and reviews that quality is met. Reports NCRs to client if occurs. Risks: project manager creates, updates and maintain risks matrix through project lifetime and ensures that risks are updated regularly with the team. Leads risk mitigation action. Tracking & reporting: Project managers creates metric for internal and external tracking of the project and ensures the quality of the data and the countermeasures/improvements to apply in the event of deviations. Projects managers provide regular reporting to client and to board Tasks Project setup and project plan Budget responsibility Planning responsibilities Quality planning & improvement Client satisfaction & relation Internal reporting and information Keep track of information within project Process reports by collecting, analysing and summarizing data Contributing to client tenders (schedule, cost and price calculations) Report follow up of project against budget (hours, materials, etc) Identify deviations of budget and prepare countermeasures Create KPIs for each project and evaluate project progress against the KPIs Coordination & Internal/External Communication The Project manager coordinate and leads project team to achieve all needed scope according to client requirements during all stages of the project (design, development, qualification, production) and through all company departments. The Project Manager summarizes works to be done and communicates the work to the specific team (Sr. Engineer, Lead production, etc….) The Project Manager writes and presents project reports to the board. Project Manager must have both clear verbal and written skills to provide information to the team and to the client The Project Manager is capable of supporting commercial managers by providing good presentable information and also can give technical substantiations to client in client meetings. The Project Manager writes understandable technical reports and/or progress reports for clients. Knowledge and Experience Education: min. Bachelor degree in Technical education. Experience: minimum 5 year relevant experience in engineering, project manager or related profession, preferably in the Aeronautic / Aerospace market Experience in supplier-client relationship Experience with project activities and management (PMP) Experience in leading engineering and production teams Additional knowledge of composite production methods and engineering is a plus Advanced knowledge of English and Spanish/Catalan language Software skills: Knowledge of ERP & Windows & Office suite, 3D CAD Conditions Permanent contract Salary package according to experience and value Flexible working time between monday to friday 8:00/9:00 - 17:00/18:00h Career plan in aeronautic & aerospace sector

As part of the Strategic Initiative, ICFO coordinates PIXEurope, a flagship Pilot Line funded under the European Chips JU program. With €400 million in investments and a consortium of 20 partners across 11 countries, the project aims to reinforce Europe’s strategic autonomy in photonic technologies and accelerate industrial uptake of cutting-edge integrated photonics. Over the next decade, PIXEurope will enable the transfer of advanced technologies to manufacturing environments, while fostering innovation and scalability across the European photonics ecosystem. Desplácese hacia abajo para encontrar una descripción detallada de este trabajo y lo que se espera de los candidatos. Envíe su solicitud haciendo clic en el botón "Solicitar". POSITION OVERVIEW ICFO is seeking a Procurement Technician to support the operational deployment of the PIXEurope pilot line. The selected candidate will be responsible for managing the procurement needs of the project – including public tenders, orders, deliveries, and associated documentation – and providing basic legal counsel support to ensure that contracts and agreements are properly executed. The Procurement Technician will work closely with the Pilot Line Procurement and Financial Manager, the technical staff to establish requirements and provide procurement and legal guidance, and the Director of the Strategic Initiative. The role will also involve close collaboration with ICFO’s Legal Team, Projects Financial Control Team, and Finance Team. The position will operate under the supervision of the Legal Team – particularly the procurement staff – who will ensure that all activities are carried out in full alignment with ICFO’s internal procedures and compliance requirements. KEY RESPONSIBILITIES • Manage all phases of procurement procedures for the PIXEurope pilot line, from planning and tender preparation to delivery and invoicing., • Work with technical staff to define requirements, advise on procurement options, and ensure timely acquisition of goods and services., • Prepare and publish tender documents in compliance with public procurement regulations and ICFO’s internal policies., • Coordinate the evaluation of offers and preparation of contractual and administrative documentation., • Liaise with suppliers, project partners, and internal stakeholders to ensure timely and accurate execution of procurement processes., • Maintain accurate and organized procurement and contractual records in both physical and electronic formats., • Provide the Pilot Line with basic legal counsel support, including reviewing and preparing project-related contracts, agreements, and memorandums of understanding., • Support in audits and financial justification for public/European funding. QUALIFICATIONS AND EXPERIENCE REQUIRED The ideal candidate will bring: • A university degree in Law, Business Administration, Political Science, or a related discipline., • At least 2 years of experience in public procurement or contract management, ideally in the public sector or a research environment., • Knowledge of the Spanish Public Sector Contracts Law and procurement procedures., • Fluency in English, Spanish, and Catalan (written and spoken)., • Strong organizational, communication, and problem-solving skills., • Proficiency with office and collaborative tools (e.g., MS Office, Teams, SharePoint). Additional skills and experience that will be valued: • Knowledge of legal counsel functions in a project-based environment., • Experience in procurement of scientific or technical equipment., • Familiarity with EU-funded projects (e.g., Horizon Europe, Chips JU) – valued but not required., • Experience in process optimization and continuous improvement of procurement tools and workflows. WHAT WE OFFER • Indefinite contract for scientific and technical activities pursuant to Spanish Law 14/2011, linked to the duration of the Pilot Line initiative., • A unique opportunity to shape and drive a high-impact European initiative at the forefront of photonic innovation., • Integration into a vibrant, international, and multidisciplinary environment at ICFO., • Integration into ICFO’s vibrant, multidisciplinary, and international research community., • A strategic position in a project that will define the future of European photonics., • A competitive salary according to ICFO’s internal scales and a family allowance, if applicable, in line with institutional policy. APPLICATION PROCESS To apply, please submit your resume, a cover letter outlining your experience and contact information for two professional references. Applications should be submitted via LinkedIn or the ICFOjobs platform will include a pre-screening of applicants based on eligibility and experience, followed by an interview with a short-list of candidates. Candidates will be notified of the outcome within 15 days of the interview. ICFO is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. For updated information about ICFO, please visit is co-funded by the Chips Joint Undertaking and national funding authorities of the Participating States, Spain, Ireland, The Netherlands, Finland, Belgium, Portugal, Poland, Austria , France, Italy, United Kingdom. xcskxlj In particular, it is co-funded by Spain through the Ministry for Digital Transformation and Civil Service under reference CJU- , as part of the Recovery, Transformation and Resilience Plan (PRTR).

About us: As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. Presente su candidatura después de leer los siguientes requisitos de habilidades y cualificaciones para este puesto. About the role We’re looking for a detail‑driven Group Controller to support financial controls, group consolidation, and forecasting activities across our subsidiaries. This role plays a key part in ensuring compliance, improving processes, and enhancing financial visibility across the Group. Responsibilities • Preparation of the financial aspects of new projects, • Preparation of periodic financial projections for the Group, • Ensure full compliance with transfer pricing regulations and maintain the Group’s transfer pricing manual (system), • Preparation and monitoring of the Group’s business plan, • Support in the monthly preparation and periodic projection of production costs and valued inventories, • Support in the Group's monthly accounting consolidation process, • Prepare and support the submission of financial information to the external regulatory bodies, including the Spanish Tax Agency (AEAT) and the Bank of Spain, • Collaborate with other finance areas and provide analytical and reporting support as required, • Contribute to process optimisation and projects aligned with department and company priorities About you • Bachelor's degree in finance, accounting, or a related field, • Background in manufacturing finance control role is essential, • Excellent analytical and process-optimisation skills, • Strong administrative accounting knowledge and experience, including financial control principles, • Strong proficiency in Microsoft Excel and experience using ERP system, • Professional level English (verbal and written), • Self-motivated and proactive approach to achieving deadlines, • Strong communication, influencing skills and experience collaborating with global stakeholders What’s next? If this sounds like a role that you would be interested in, then we would love to hear from you. Please apply with a copy of your CV in English to allow your application to be considered. Closing Date: 3/4/2026 Please note, closing dates are subject to change and, at times of high volume of applications, this may be brought forward. Please note this is a Direct Search led by Bioiberica. Applications from agencies will not be accepted nor will fees be paid for unsolicited CVs. Equality and diversity at Bioiberica / SARIA's group of companies We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background. We expressly welcome applications from people with a wide range of perspectives and experiences. xcskxlj Our goal is to ensure equal opportunities and actively combat discrimination – both in the application process and in everyday working life.

Position Title: Business Development Manager (Enterprise Hunter) Solicitar este puesto es sencillo. Desplácese hacia abajo y haga clic en "Solicitar" para ser considerado para esta posición. GTT is a leading global provider of secure cloud networking solutions for multinational organizations. We design and deliver solutions that leverage advanced cloud, networking and security technologies. We complement our solutions with a suite of professional services and exceptional sales and support teams in local markets around the world. We serve thousands of national and multinational companies with a portfolio that includes SD-WAN, security, Internet, voice and other connectivity options. Our services are uniquely enabled by our top-ranked, global, Tier 1 IP backbone, which spans more than 260 cities on six continents. The company culture is built on a customer-first service experience reinforced by our commitment to operational excellence and continuous improvement in our business, environmental, social and governance practices. The Business Development Manager (Enterprise Hunter) will be responsible for managing the contact plan, approach strategy and full sales cycle to deliver further revenue growth across our SD-WAN and SASE product lines. Job Scope/Supervision: Drive opportunities from discovery, through development to close Driven by new logo acquisition Agile in a fast-paced environment Good organisational awareness, planning skills and collaboration Excellent written and verbal English communication skills Hours/Travel/Shift: Office hours Business Acumen: Knowledge of business concepts, tools, and processes that are needed for making sound decisions in the context of the company's business; Networking: Understanding of the business value of creating mutually beneficial relationships with individuals outside of incumbent's own organization and ability to generate productive relationships with internal and external partners that improve access to resources and expertise. Knowledge of transformation initiatives to drive fundamental changes, enhance responsiveness and efficiency to core business practices. Ability to drive cultural changes from best effort to results oriented GTT provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. In addition to federal law requirements, GTT complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. xcskxlj GTT expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status.

Job Summary The main responsibility of the Financial Analyst is to provide accurate and data based information on company’s financial performance, in order to help company make well informed decisions. The position involves overseeing accounting processes and producing relevant financial reports and recommendations. Key Accountabilities • Monthly closing and reporting for the assigned entities:, • Prepare and post month end accruals., • Review accounting operations, including billing, A/R, A/P, cost accounting, inventory accounting, revenue recognition, etc., • Reconcile transactions by comparing and correcting data., • Reconcile Intercompany transactions., • Reporting package: P&L’s, Cash Flow, BS, Investment, Capex, Headcount, …, • Manage and comply with local government reporting requirements and tax filings., • Tracking of operating expenses., • Preparation of operational performance reports with recommendations for corrective action. Identification of opportunities to improve financial performance., • Implement and monitor policies and procedures., • Collaborate with external auditing services to ensure proper compliance with all regulations., • Other external reporting to Government bodies., • Transfer pricing analysis of the intercompany transactions., • Reporting of Non Financial Information., • Continuous improvement of the quality, reliability and responsiveness of the information provided. Networking/Key relationships The position requires interaction with: • Different company departments (Administration, Logistics, HR, Finance, Accounting, IT, Legal & Tax, Internal Audit, Sales & Marketing…)., • The affiliates of the Group., • Management., • Third parties as auditors and consultants. Minimum Knowledge & Experience required for the position: • Bachelors’ and/or MBA degree in Finance, Economics or related field., • 4+ years’ experience in accounting and finance (auditing, consulting, industry, …)., • Knowledge and experience in tax accounting and/or Non Financial Information reporting will be valued., • Proficient in spreadsheets (i.e. Excel), databases, MS Office and financial software applications., • Knowledge and experience with SAP and/or EPM tools (e.g OneStream) would be an advantage., • Fluent in Spanish and English. Skills & Capabilities: • Accounting and financial expertise., • Able to analyze, organize, summarize and articulate complex financial information., • Problem solving, creativity and proactivity., • Process analysis and process improvement; procedure development., • Team work, communicative., • Task and goal oriented and ability to influence and guide decision makers., • Flexibility and adaptability. Able to prioritize and work in multiple tasks with multiple supervisors., • Confidential, credible, ethical. Travel requirements: No required

We are Impress. We believe everyone deserves a smile they’ll love. We are the largest chain of ortho clinics with fully digital processes. We have revolutionized the invisible orthodontic sector with the best team of professionals specialized in making people smile and using the latest technology for the diagnosis, treatment, and follow-up of all cases. Born in Barcelona in 2019, in just 7 years, we’ve grown to pioneer leading care, flagship clinics and state-of-the-art tech across 10 countries and more than 150 locations, and we are expanding fast! Our aim is to improve people’s health and quality of life across the globe. We’re looking for an International Tax Specialist to join our Finance team and report directly to the Tax Director. You’ll play a key role in shaping the future of the tax function – helping to deliver our roadmap and driving process improvements across the business. Key Responsibilities: • Be responsible for all Group tax compliance and reporting (Europe and USA), • Support technical international tax projects on an ad-hoc basis., • Coordinate with other departments to streamline tax processes., • Keep up to date with changes in tax legislation and its impact on the Group., • Partner with the Tax Director and wider teams on ad-hoc research, VAT and transfer pricing projects, and new projects., • Handle audits, appeals, or formal dispute resolution processes, • Manage relationships with external advisors., • Prepare tax disclosures for statutory accounts, and act as the bridge between the tax and finance functions. You’ll Bring: • Minimum 5+ years of experience in international tax ideally within a multinational group or advisory firm., • Excellent understanding of tax accounting and compliance processes, • Advanced problem-solving skills with a results-driven, get-things-done attitude., • A proactive, hands-on approach and a “can-do” attitude., • Strong multitasking abilities to manage competing priorities., • Strong communication and stakeholder management skills. Comfortable working in a fast-paced environment., • High attention to detail and excellent organization skills., • A collaborative mindset – a big thinker with a small ego., • Fluent in English, proactive and comfortable in a fast-paced, dynamic environment. What we offer: • Opportunity to grow in an innovative company and Top International Scale Up., • Attractive Compensation package., • Flexibility on attendance hours (starting 8am to 10am from Monday to Friday)., • Benefits with our treatments, aligners, and products., • Collaborative work environment and positive culture., • International and diverse teams., • Coffee, free gym access every day in our central located office. Due to the impossibility of providing sponsorship, we require you to have the eligibility to work in the EU At Impress we cultivate a culture of inclusion and diversity. We celebrate our employees' individual strengths, views, and experiences and we encourage all candidates to apply, without regard to race, color, religion, gender identity, sexual orientation, age, national origin, disability, or any other factor. Our differences enable us to be a better team – one that makes better decisions, drives innovation, and delivers better results.

Hybrid 50%. Our client is a science-led ingredients manufacturer entering an exciting new stage of commercial expansion. We are seeking a Client Acquisition Executive to identify, prospect, and qualify new business opportunities that will support continued global growth. In this position, you will be responsible for generating new leads and creating a consistent flow of qualified business opportunities across international markets. Conduct proactive commercial outreach through calls, emails, and networking activities. Qualify new leads and transfer them to Inside Sales and Sales Managers. Build and manage a structured sales pipeline, tracking progress against KPIs and timelines. Collaborate closely with Inside Sales, Sales Managers, and Marketing to ensure strong lead conversion. Previous experience in business development, inside sales, or sales prospecting. Communication skills in both Spanish and English. This is an excellent opportunity for a motivated sales professional who is eager to grow their career in international sales with an innovative & growing company.

We are Impress. We believe everyone deserves a smile they'll love. We are the largest chain of ortho clinics with fully digital processes. We have revolutionized the invisible orthodontic sector with the best team of professionals specialized in making people smile and using the latest technology for the diagnosis, treatment, and follow-up of all cases. Born in Barcelona in 2019, in just 7 years, we've grown to pioneer leading care, flagship clinics and state-of-the-art tech across 10 countries and more than 150 locations, and we are expanding fast Our aim is to improve people's health and quality of life across the globe. We're looking for an International Tax Specialist to join our Finance team and report directly to the Tax Director. You'll play a key role in shaping the future of the tax function – helping to deliver our roadmap and driving process improvements across the business. Key Responsibilities: Be responsible for all Group tax compliance and reporting (Europe and USA) Support technical international tax projects on an ad-hoc basis. Coordinate with other departments to streamline tax processes. Keep up to date with changes in tax legislation and its impact on the Group. Partner with the Tax Director and wider teams on ad-hoc research, VAT and transfer pricing projects, and new projects. Handle audits, appeals, or formal dispute resolution processes Manage relationships with external advisors. Prepare tax disclosures for statutory accounts, and act as the bridge between the tax and finance functions. You'll Bring: Minimum 5+ years of experience in international tax ideally within a multinational group or advisory firm. Excellent understanding of tax accounting and compliance processes Advanced problem-solving skills with a results-driven, get-things-done attitude. A proactive, hands-on approach and a can-do attitude. Strong multitasking abilities to manage competing priorities. Strong communication and stakeholder management skills. Comfortable working in a fast-paced environment. High attention to detail and excellent organization skills. A collaborative mindset – a big thinker with a small ego. Fluent in English, proactive and comfortable in a fast-paced, dynamic environment. What we offer: Opportunity to grow in an innovative company and Top International Scale Up. Attractive Compensation package. Flexibility on attendance hours (starting 8am to 10am from Monday to Friday). Benefits with our treatments, aligners, and products. Collaborative work environment and positive culture. International and diverse teams. Coffee, free gym access every day in our central located office. Due to the impossibility of providing sponsorship, we require you to have the eligibility to work in the EU At Impress we cultivate a culture of inclusion and diversity. We celebrate our employees' individual strengths, views, and experiences and we encourage all candidates to apply, without regard to race, color, religion, gender identity, sexual orientation, age, national origin, disability, or any other factor. Our differences enable us to be a better team – one that makes better decisions, drives innovation, and delivers better results.

We are seeking a Deployment Engineer to support complex gateway deployment operations and ensure a seamless transition from construction to live network operations. This role plays a critical part in delivering operational excellence across international telecommunications infrastructure projects. The successful candidate will combine technical understanding with strong coordination and documentation capabilities. About the Role You will manage deployment documentation, coordinate multidisciplinary technical activities, oversee schedules, and ensure full operational readiness prior to service activation. Acting as a bridge between construction, RF engineering, network operations centers (NOC), and field services teams, you will ensure infrastructure is delivered on time, compliant, and ready for integration into live service environments. Responsibilities Documentation & Acceptance Readiness Prepare comprehensive acceptance packages including technical specifications, test results, and compliance documentation Maintain accurate documentation throughout the deployment lifecycle Coordinate configuration validation and acceptance testing activities Ensure regulatory, safety, and technical prerequisites are completed for timely activation Technical Coordination & Deployment Tracking Track critical technical tasks and identify schedule risks or resource conflicts Coordinate across engineering, construction, NOC, and field services teams Provide milestone reporting and manage escalations Align technical execution with project timelines and delivery baselines Operational Handover & Transition Validate completion of commissioning activities before operational handover Confirm readiness for service activation and monitoring integration Prepare operational procedures, maintenance schedules, and technical references Support structured knowledge transfer to operational support teams Quality Assurance & Process Improvement Monitor compliance with deployment and change management procedures Identify documentation or process gaps and support continuous improvement initiatives Assist in developing standardized templates and delivery frameworks Participate in post-deployment reviews and implement lessons learned Qualifications Bachelor’s degree in Engineering, Telecommunications, IT, or related technical field Associate degree with relevant experience considered Required Skills Minimum 2+ years in service delivery, network deployment, or technical project coordination Experience within telecommunications or connectivity infrastructure environments Strong background in documentation control and cross-functional coordination Spanish and English Professional Proficiency is a must. Preferred Skills Understanding of deployment processes and gateway infrastructure systems Experience with change management and acceptance testing workflows Familiarity with configuration management and documentation control systems Knowledge of service handover and operational transition processes Pay range and compensation package Location: Based in Spain or the UK. Work authorization required. Flexibility expected for working hours to coordinate with global teams. Occasional off-hours or weekend availability during activation or transition phases. Occasional travel required for key deployment milestones. Equal Opportunity Statement We are committed to diversity and inclusivity.

Hybrid 50%. Our client is a science-led ingredients manufacturer entering an exciting new stage of commercial expansion. We are seeking a Client Acquisition Executive to identify, prospect, and qualify new business opportunities that will support continued global growth. In this position, you will be responsible for generating new leads and creating a consistent flow of qualified business opportunities across international markets. Conduct proactive commercial outreach through calls, emails, and networking activities. Qualify new leads and transfer them to Inside Sales and Sales Managers. Build and manage a structured sales pipeline, tracking progress against KPIs and timelines. Collaborate closely with Inside Sales, Sales Managers, and Marketing to ensure strong lead conversion. Previous experience in business development, inside sales, or sales prospecting. Communication skills in both Spanish and English. This is an excellent opportunity for a motivated sales professional who is eager to grow their career in international sales with an innovative & growing company.

We are Impress. We believe everyone deserves a smile they'll love. We are the largest chain of ortho clinics with fully digital processes. We have revolutionized the invisible orthodontic sector with the best team of professionals specialized in making people smile and using the latest technology for the diagnosis, treatment, and follow-up of all cases. Born in Barcelona in 2019, in just 7 years, we've grown to pioneer leading care, flagship clinics and state-of-the-art tech across 10 countries and more than 150 locations, and we are expanding fast Our aim is to improve people's health and quality of life across the globe. We're looking for an International Tax Specialist to join our Finance team and report directly to the Tax Director. You'll play a key role in shaping the future of the tax function – helping to deliver our roadmap and driving process improvements across the business. Key Responsibilities: Be responsible for all Group tax compliance and reporting (Europe and USA) Support technical international tax projects on an ad-hoc basis. Coordinate with other departments to streamline tax processes. Keep up to date with changes in tax legislation and its impact on the Group. Partner with the Tax Director and wider teams on ad-hoc research, VAT and transfer pricing projects, and new projects. Handle audits, appeals, or formal dispute resolution processes Manage relationships with external advisors. Prepare tax disclosures for statutory accounts, and act as the bridge between the tax and finance functions. You'll Bring: Minimum 5+ years of experience in international tax ideally within a multinational group or advisory firm. Excellent understanding of tax accounting and compliance processes Advanced problem-solving skills with a results-driven, get-things-done attitude. A proactive, hands-on approach and a can-do attitude. Strong multitasking abilities to manage competing priorities. Strong communication and stakeholder management skills. Comfortable working in a fast-paced environment. High attention to detail and excellent organization skills. A collaborative mindset – a big thinker with a small ego. Fluent in English, proactive and comfortable in a fast-paced, dynamic environment. What we offer: Opportunity to grow in an innovative company and Top International Scale Up. Attractive Compensation package. Flexibility on attendance hours (starting 8am to 10am from Monday to Friday). Benefits with our treatments, aligners, and products. Collaborative work environment and positive culture. International and diverse teams. Coffee, free gym access every day in our central located office. Due to the impossibility of providing sponsorship, we require you to have the eligibility to work in the EU At Impress we cultivate a culture of inclusion and diversity. We celebrate our employees' individual strengths, views, and experiences and we encourage all candidates to apply, without regard to race, color, religion, gender identity, sexual orientation, age, national origin, disability, or any other factor. Our differences enable us to be a better team – one that makes better decisions, drives innovation, and delivers better results.

We are Impress. We believe everyone deserves a smile they'll love. We are the largest chain of ortho clinics with fully digital processes. We have revolutionized the invisible orthodontic sector with the best team of professionals specialized in making people smile and using the latest technology for the diagnosis, treatment, and follow-up of all cases. Born in Barcelona in 2019, in just 7 years, we've grown to pioneer leading care, flagship clinics and state-of-the-art tech across 10 countries and more than 150 locations, and we are expanding fast Our aim is to improve people's health and quality of life across the globe. We're looking for an International Tax Specialist to join our Finance team and report directly to the Tax Director. You'll play a key role in shaping the future of the tax function – helping to deliver our roadmap and driving process improvements across the business. Key Responsibilities: Be responsible for all Group tax compliance and reporting (Europe and USA) Support technical international tax projects on an ad-hoc basis. Coordinate with other departments to streamline tax processes. Keep up to date with changes in tax legislation and its impact on the Group. Partner with the Tax Director and wider teams on ad-hoc research, VAT and transfer pricing projects, and new projects. Handle audits, appeals, or formal dispute resolution processes Manage relationships with external advisors. Prepare tax disclosures for statutory accounts, and act as the bridge between the tax and finance functions. You'll Bring: Minimum 5+ years of experience in international tax ideally within a multinational group or advisory firm. Excellent understanding of tax accounting and compliance processes Advanced problem-solving skills with a results-driven, get-things-done attitude. A proactive, hands-on approach and a can-do attitude. Strong multitasking abilities to manage competing priorities. Strong communication and stakeholder management skills. Comfortable working in a fast-paced environment. High attention to detail and excellent organization skills. A collaborative mindset – a big thinker with a small ego. Fluent in English, proactive and comfortable in a fast-paced, dynamic environment. What we offer: Opportunity to grow in an innovative company and Top International Scale Up. Attractive Compensation package. Flexibility on attendance hours (starting 8am to 10am from Monday to Friday). Benefits with our treatments, aligners, and products. Collaborative work environment and positive culture. International and diverse teams. Coffee, free gym access every day in our central located office. Due to the impossibility of providing sponsorship, we require you to have the eligibility to work in the EU At Impress we cultivate a culture of inclusion and diversity. We celebrate our employees' individual strengths, views, and experiences and we encourage all candidates to apply, without regard to race, color, religion, gender identity, sexual orientation, age, national origin, disability, or any other factor. Our differences enable us to be a better team – one that makes better decisions, drives innovation, and delivers better results.

Hybrid 50%. Our client is a science-led ingredients manufacturer entering an exciting new stage of commercial expansion. We are seeking a Client Acquisition Executive to identify, prospect, and qualify new business opportunities that will support continued global growth. In this position, you will be responsible for generating new leads and creating a consistent flow of qualified business opportunities across international markets. Conduct proactive commercial outreach through calls, emails, and networking activities. Qualify new leads and transfer them to Inside Sales and Sales Managers. Build and manage a structured sales pipeline, tracking progress against KPIs and timelines. Collaborate closely with Inside Sales, Sales Managers, and Marketing to ensure strong lead conversion. Previous experience in business development, inside sales, or sales prospecting. Communication skills in both Spanish and English. This is an excellent opportunity for a motivated sales professional who is eager to grow their career in international sales with an innovative & growing company.

At Rob Surgical we are looking to hire a Process Engineering Quality Assurance Technician to join our Quality team and support the continuous improvement and validation of our manufacturing and quality processes. 🧬 About us We are a healthtech company specialized in the development of advanced robotic systems for high-precision minimally invasive surgery. Founded in 2012 as a spin-off from UPC and IBEC, our mission is clear: to make robot-assisted surgery more accessible, precise, and efficient worldwide. 🔍 What will your mission be? As a Process Engineering QA Technician, you will play a key role in ensuring the effectiveness of our Quality Management System (QMS) by supporting the validation master plan, calibration program, and process quality activities. You will work closely with product managers, project managers, developers, and manufacturing teams to ensure quality and regulatory compliance across the entire product lifecycle. 🛠 Your main responsibilities will include: Quality Management System • Drafting and reviewing documentation related to QMS processes., • Participating in the maintenance of risk analyses for QMS processes., • Monitoring and maintaining quality KPIs., • Conducting regular inspections in the production plant to verify process control and compliance with procedures., • Organizing and participating in quality meetings., • Supporting the transfer from design to production, including control plans and control methods., • Training manufacturing personnel when required., • Supporting the design and construction of test rigs for design and manufacturing validation., • Writing validation protocols and reports., • Participating in validation execution and monitoring progress of the validation plan., • Preparing validation maintenance reports and monitoring equipment, facilities, and services., • Participating in validations related to:, • Clean rooms, • Ethylene oxide and wet steam sterilization systems, • Computerized systems, • Analytical test methods, • Maintaining and updating facility and process risk analyses., • Monitoring the calibration program and reporting progress., • Developing and updating calibration procedures., • Participating in calibration activities and issuing calibration reports., • Supporting internal and external audits., • Collaborating in the preparation of annual R&D reports and department budgets., • Supporting administrative tasks related to documentation, digitalization, and archiving., • Contributing to maintaining an organized and efficient work environment. 🎓 What are we looking for? • Bachelor’s degree in Industrial Engineering is highly valued., • Experience level: 3+ years of experience, • Experience in medical devices and/or pharmaceutical industry is highly valued., • Professional working proficiency in English., • Advanced Microsoft Office user., • Experience working with ERP environments. 📚 Valuable knowledge Experience or training related to: • ISO 17025 – Calibration laboratories, • ISO 14644 – Clean rooms, • ISO 11135 / ISO 14937 – Sterilization of medical devices, • ISO 14971 – Risk management for medical devices, • GAMP5 – Validation of computerized systems, • GMP and validation regulations, • Metrology or microbiology 💡 We are looking for someone who is… • Detail-oriented but able to understand the big picture., • Analytical, proactive, and collaborative., • Meticulous, organized, and efficient., • A strong communicator with teamwork. 🎯 What do we offer? • Full-time permanent contract., • Salary aligned with profile and experience., • Flexible working hours., • Monthly fruit and vegetable box 🍎, • Opportunity to work on cutting-edge surgical robotics technology., • Professional development in a highly innovative and regulated environment., • A dynamic and collaborative team where your work has real impact on patients’ lives.

R&D Manager - Medical Devices (High‑Risk Class III) - Freelance (6 Months) Location: Barcelona, Spain (On‑Site) Contract: 6‑month freelance contract with the possibility of a permanent offer Industry: High‑Risk Medical Devices About the Role We are seeking an experienced R&D Manager to lead the development of high‑risk Class III medical devices-specifically balloon catheters, vascular stents, or comparable interventional products. You will manage a multidisciplinary team of engineers and drive projects from early‑stage feasibility through design, verification, qualification, and transfer to manufacturing. Spanish language skills are not required. Full‑time on‑site presence in Barcelona is essential. Key Responsibilities R&D Leadership & Team Management • Lead and mentor a team of R&D engineers, providing technical direction, workload prioritization, and performance development., • Oversee daily engineering activities including design iterations, prototyping, test planning, and documentation., • Establish and enforce robust engineering processes aligned with global regulatory expectations. Design & Development of High‑Risk Devices • Own the full design life cycle, from concept development and feasibility testing through to final design freeze., • Drive detailed engineering work for balloon catheters, stents, or similar interventional devices, including:, • Balloon forming and bonding processes, • Stent design, coatings, and mechanical performance, • Catheter shaft architecture and material selection, • Tolerance analysis, DFM/A, material characterisation, • Lead Verification & Validation (V&V) strategy, including test method development, equipment qualification, and protocol/report generation. Qualification & Industrialisation • Manage design qualification, including performance testing, biocompatibility considerations, sterilisation validation input, and packaging qualification., • Oversee transfer of designs into manufacturing / scale‑up, collaborating with process engineering and suppliers. Project & Stakeholder Management • Act as project owner for multiple R&D programmes, managing timelines, budgets, risk registers, and resource allocation., • Coordinate with Quality, Regulatory, Clinical, and Operations teams to ensure coherent project execution., • Present project updates to leadership, aligning on strategy, risks, and technical decisions. Regulatory & Compliance (FDA and MDR) • Ensure all R&D activities adhere to Design Control requirements under 21 CFR 820 and EU MDR., • Lead or contribute to core regulatorydeliverables, including:, • Design History File (DHF), • Risk Management File (ISO 14971), • Design Inputs/Outputs, • Verification/Validation documentation, • Support regulatory submissions through technical report preparation and cross‑functional input. Required Experience • Minimum 3 years' experience in R&D management within the medical device sector., • Proven hands‑on experience with high‑risk Class III devices, preferably balloon catheters or stents., • Demonstrated ability to lead engineering teams and manage complex technical projects., • Strong understanding of Design Controls, Risk Management, V&V, and qualification activities., • Proficiency with FDA 21 CFR 820, EU MDR, ISO 13485, and ISO 14971., • Excellent organisational and communication skills., • Ability to work full‑time on site in Barcelona.

BioSystems diseña, desarrolla, fabrica y comercializa soluciones analíticas, creando tanto pruebas de reactivos como instrumentación analítica para laboratorios de diagnóstico in vitro (IVD), así como para fines industriales. Nuestro objetivo es mejorar la salud y el bienestar en todo el mundo. Para ello, desarrollamos soluciones, basadas en el concepto de Una Única Salud, para: • Salud humana, • Salud animal, • Salud alimentaria, • Salud ambiental, • Y a través de bioprocesos Somos una empresa global, que opera en más de 100 mercados a través de distribuidores y con empresas en 17 países. Esto nos permite estar cerca de las personas usuarias de nuestros productos, brindando la mejor atención posible y asegurando que nuestro servicio técnico llegue a clientes de todo el mundo. Buscamos una persona para participar en la transferencia del Diseño y Desarrollo de Productos desde la R+D+i al entorno de producción de la empresa, y con capacidad de integrarse en equipos multidisciplinares de diferentes áreas. La transferencia es la conversión de los resultados de la investigación y el desarrollo en información válida (documentos, instrucciones) para poder fabricar, controlar y comercializar el producto desarrollado. Responsabilidades: • Participar en la definición y realizar el proceso de implantación de los resultados del diseño al sistema de gestión de la empresa., • Preparar y adaptar parte de la documentación necesaria para la fabricación, control y comercialización de productos., • Coordinar a las personas que participan en las fases finales del desarrollo, validación y lanzamiento de nuevos productos., • Gestionar la documentación del control del diseño (requisitos de producto, gestión de riesgos, planes e informes de validación)., • Liderar proyectos de digitalización de acceso a la documentación técnica de productos teniendo en cuenta la experiencia de usuario. Requisitos: • Titulación universitaria de grado superior en disciplinas relacionadas con ciencias de la vida (Biotecnología, Bioquímica, Biología, Química, Biomedicina…)., • Experiencia de al menos un año en puestos de trabajo y actividades similares como laboratorios clínicos o en puestos de Quality Assurance. Persona habituada a trabajar en entornos reglamentados tipo ISO., • Inglés fluido., • Se valorará estar familiarizado en digitalización de procesos., • Se valorará conocimientos de Excel avanzado (macros, tablas dinámicas). Habilidades requeridas: • Organización, orden y rigurosidad en el trabajo., • Trabajo en equipo., • Iniciativa y responsabilidad para resolver problemas. Ofrecemos: ⏰ Horario: 39h semanales 🏡 Localización: Barcelona, Sant Andreu 🏃 Fecha incorporación: inmediata ☀️ Entorno empresarial que fomenta la innovación, la participación y el crecimiento 🌱 Contrato eventual, con posibilidad de pasar a indefinido.

Protekting was founded in 2014 in Barcelona.The company started as a trading company for phytosanitary products, and quickly opened to all kind of agriculture solutions. We are focused on products and services that help our clients protect and grow crops efficiently. We are strongly committed to our clients’ needs as well as to the responsible use of products for agriculture. Although we are a young team, we have a lot of experience in the world of plant protection. We are flexible, innovative, passionate and focused on protekting our clients and partners’ interests, by helping them to grow their business. Here’s the lowdown on what your role will actually look like (spoiler alert: it’s awesome!) We are seeking for Laboratory Analyst to join our Team. What you'll be rocking: • Analysis of samples from all stage of the development process., • Responsible for the reporting of data., • Collaborate in the transfer of analytical methods., • Collaborate in development and validation of new analytical methods for active phytosanitary ingredients and finished formulated products., • Collaborate in the analysis and evaluation of the developing products for dossier submission., • Maintain all records in compliance with SOPs and Policies., • Writing technical reports and Standard Operating Procedures (protocols, specifications and reports). Preparation of SOP’s for General Laboratory. Practice and Laboratory Instruments., • Management and collaboration in general tasks of laboratory (equipments, standards, control of stocks..) What you bring to the table: • Basic laboratory skills and research experience of most of the following analytical techniques: HPLC, UV, UPLC, LC-MS, GC-MS, PSD, potentiometric titration, KF titration andIR., • Knowledge of analytical method transfers., • Experience MS Office. Educational milestone: • Degree in life sciences., • Qualified in Analytical Development., • Excellent level of English and Spanish, spoken and written. Your key superpowers: • Self-sufficient., • Strong analytical skills and problem solving., • Highly responsible and capable to work under pressure to meet deadlines., • Ability to prioritize multiple tasks., • Good team player., • Strong organizational, planning and time management skills, to archive project timelines., • Detail oriented and good communication and research skills., • Motivated, proactive, dynamic, methodical, organized and decisive. We’re looking for someone who works hard, plays hard, and laughs harder. Sound like you? Come aboard. Believe in life

Compensation: €30k base salary + 30% bonus target. €42k total earning potential. Location: Barcelona. Hybrid 50%. Our client is a science-led ingredients manufacturer entering an exciting new stage of commercial expansion. We are seeking a Client Acquisition Executive to identify, prospect, and qualify new business opportunities that will support continued global growth. The Role In this position, you will be responsible for generating new leads and creating a consistent flow of qualified business opportunities across international markets. • Identify and research potential new customers across EMEA and APAC., • Conduct proactive commercial outreach through calls, emails, and networking activities., • Qualify new leads and transfer them to Inside Sales and Sales Managers., • Build and manage a structured sales pipeline, tracking progress against KPIs and timelines., • Collaborate closely with Inside Sales, Sales Managers, and Marketing to ensure strong lead conversion. The Requirements • Previous experience in business development, inside sales, or sales prospecting. B2B preferred., • Communication skills in both Spanish and English., • Ability to research markets, identify key decision makers, and map accounts effectively., • Persistent and resilient approach to prospecting and overcoming rejection. This is an excellent opportunity for a motivated sales professional who is eager to grow their career in international sales with an innovative & growing company. Please apply if interested, or contact me directly via LinkedIn or .

Compensation: €30k base salary + 30% bonus target. €42k total earning potential. Location: Barcelona. Hybrid 50%. Our client is a science-led ingredients manufacturer entering an exciting new stage of commercial expansion. We are seeking a Client Acquisition Executive to identify, prospect, and qualify new business opportunities that will support continued global growth. The Role In this position, you will be responsible for generating new leads and creating a consistent flow of qualified business opportunities across international markets. • Identify and research potential new customers across EMEA and APAC., • Conduct proactive commercial outreach through calls, emails, and networking activities., • Qualify new leads and transfer them to Inside Sales and Sales Managers., • Build and manage a structured sales pipeline, tracking progress against KPIs and timelines., • Collaborate closely with Inside Sales, Sales Managers, and Marketing to ensure strong lead conversion. The Requirements • Previous experience in business development, inside sales, or sales prospecting. B2B preferred., • Communication skills in both Spanish and English., • Ability to research markets, identify key decision makers, and map accounts effectively., • Persistent and resilient approach to prospecting and overcoming rejection. This is an excellent opportunity for a motivated sales professional who is eager to grow their career in international sales with an innovative & growing company. Please apply if interested, or contact me directly via LinkedIn or .

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. If you like working in a fast-paced startup environment, you are a true perfectionist and love helping others, Glovo is your pla

At Glovo we are looking for a passionate and hands-on Transfer Pricing Associate that will be part of the tax team. Be involved in the preparation of the Transfer Pricing Documentation of the Glovo Group in line with the latest OECD Guidelines. Assist the Group subsidiaries in the fulfillment of loc

BioSystems diseña, desarrolla, fabrica y comercializa soluciones analíticas, creando tanto pruebas de reactivos como instrumentación analítica para laboratorios de diagnóstico in vitro (IVD), así como para fines industriales. Nuestro objetivo es mejorar la salud y el bienestar en todo el mundo. Para ello, desarrollamos soluciones, basadas en el concepto de Una Única Salud, para: • Salud humana, • Salud animal, • Salud alimentaria, • Salud ambiental, • Y a través de bioprocesos Somos una empresa global, que opera en más de 100 mercados a través de distribuidores y con empresas en 17 países. Esto nos permite estar cerca de las personas usuarias de nuestros productos, brindando la mejor atención posible y asegurando que nuestro servicio técnico llegue a clientes de todo el mundo. Buscamos una persona para participar en la transferencia del Diseño y Desarrollo de Productos desde la R+D+i al entorno de producción de la empresa, y con capacidad de integrarse en equipos multidisciplinares de diferentes áreas. La transferencia es la conversión de los resultados de la investigación y el desarrollo en información válida (documentos, instrucciones) para poder fabricar, controlar y comercializar el producto desarrollado. Responsabilidades: • Participar en la definición y realizar el proceso de implantación de los resultados del diseño al sistema de gestión de la empresa., • Preparar y adaptar parte de la documentación necesaria para la fabricación, control y comercialización de productos., • Coordinar a las personas que participan en las fases finales del desarrollo, validación y lanzamiento de nuevos productos., • Gestionar la documentación del control del diseño (requisitos de producto, gestión de riesgos, planes e informes de validación)., • Liderar proyectos de digitalización de acceso a la documentación técnica de productos teniendo en cuenta la experiencia de usuario. Requisitos: • Titulación universitaria de grado superior en disciplinas relacionadas con ciencias de la vida (Biotecnología, Bioquímica, Biología, Química, Biomedicina…)., • Experiencia de al menos un año en puestos de trabajo y actividades similares como laboratorios clínicos o en puestos de Quality Assurance. Persona habituada a trabajar en entornos reglamentados tipo ISO., • Inglés fluido., • Se valorará estar familiarizado en digitalización de procesos., • Se valorará conocimientos de Excel avanzado (macros, tablas dinámicas). Habilidades requeridas: • Organización, orden y rigurosidad en el trabajo., • Trabajo en equipo., • Iniciativa y responsabilidad para resolver problemas. Ofrecemos: ⏰ Horario: 39h semanales 🏡 Localización: Barcelona, Sant Andreu 🏃 Fecha incorporación: inmediata ☀️ Entorno empresarial que fomenta la innovación, la participación y el crecimiento 🌱 Contrato eventual, con posibilidad de pasar a indefinido.

At Rob Surgical we are looking to hire a Process Engineering Quality Assurance Technician to join our Quality team and support the continuous improvement and validation of our manufacturing and quality processes. 🧬 About us We are a healthtech company specialized in the development of advanced robotic systems for high-precision minimally invasive surgery. Founded in 2012 as a spin-off from UPC and IBEC, our mission is clear: to make robot-assisted surgery more accessible, precise, and efficient worldwide. 🔍 What will your mission be? As a Process Engineering QA Technician, you will play a key role in ensuring the effectiveness of our Quality Management System (QMS) by supporting the validation master plan, calibration program, and process quality activities. You will work closely with product managers, project managers, developers, and manufacturing teams to ensure quality and regulatory compliance across the entire product lifecycle. 🛠 Your main responsibilities will include: Quality Management System • Drafting and reviewing documentation related to QMS processes., • Participating in the maintenance of risk analyses for QMS processes., • Monitoring and maintaining quality KPIs., • Conducting regular inspections in the production plant to verify process control and compliance with procedures., • Organizing and participating in quality meetings., • Supporting the transfer from design to production, including control plans and control methods., • Training manufacturing personnel when required., • Supporting the design and construction of test rigs for design and manufacturing validation., • Writing validation protocols and reports., • Participating in validation execution and monitoring progress of the validation plan., • Preparing validation maintenance reports and monitoring equipment, facilities, and services., • Participating in validations related to:, • Clean rooms, • Ethylene oxide and wet steam sterilization systems, • Computerized systems, • Analytical test methods, • Maintaining and updating facility and process risk analyses., • Monitoring the calibration program and reporting progress., • Developing and updating calibration procedures., • Participating in calibration activities and issuing calibration reports., • Supporting internal and external audits., • Collaborating in the preparation of annual R&D reports and department budgets., • Supporting administrative tasks related to documentation, digitalization, and archiving., • Contributing to maintaining an organized and efficient work environment. 🎓 What are we looking for? • Bachelor’s degree in Industrial Engineering is highly valued., • Experience level: 3+ years of experience, • Experience in medical devices and/or pharmaceutical industry is highly valued., • Professional working proficiency in English., • Advanced Microsoft Office user., • Experience working with ERP environments. 📚 Valuable knowledge Experience or training related to: • ISO 17025 – Calibration laboratories, • ISO 14644 – Clean rooms, • ISO 11135 / ISO 14937 – Sterilization of medical devices, • ISO 14971 – Risk management for medical devices, • GAMP5 – Validation of computerized systems, • GMP and validation regulations, • Metrology or microbiology 💡 We are looking for someone who is… • Detail-oriented but able to understand the big picture., • Analytical, proactive, and collaborative., • Meticulous, organized, and efficient., • A strong communicator with teamwork. 🎯 What do we offer? • Full-time permanent contract., • Salary aligned with profile and experience., • Flexible working hours., • Monthly fruit and vegetable box 🍎, • Opportunity to work on cutting-edge surgical robotics technology., • Professional development in a highly innovative and regulated environment., • A dynamic and collaborative team where your work has real impact on patients’ lives.

Contrato laboral formativo para la obtención de la práctica profesional con una duración de 12 meses. Imprescindible tener titulo universitario obtenido en los últimos 3 años. As an HR Intern, your main mission will be to support the HR function in Iberia with administrative tasks as well as recruitment activities, in close cooperation with our HR Business Partner. You will also support our Managing Director with administrative tasks. RESPONSIBILITIES OF THE ROLE HR administration: • Support Human Resources with the processing of employee payroll, update the payroll database with changes, and maintain payroll files., • Support employees throughout the employee lifecycle (including onboarding and offboarding administration, preparation of HR-related documents, master data maintenance in the HR tool, and maintaining complete employee files in compliance with GDPR); provide ad hoc support as needed., • Support Human Resources in the digitalization of personnel files (PeopleDoc project)., • Support global Human Resources projects and take ownership of small projects independently., • Raise purchase orders and record invoices against budgets., • Support the recruitment process., • Keep up to date the public HR SharePoint for all the employees. Managing Director Assistant • Coordinate agendas and plan the monthly Managing Committee meetings., • Send Outlook invitations for the monthly “MH Iberia Call” virtual meeting and follow up by email to collect the topics to be shared., • Support the administrative organization of Market Visits: travel and transfer arrangements, hotel bookings, and invoice/payment management., • Organize trips to Maisons for VIP customers: planning, travel arrangements, budgeting, supplier management, and logistics. PROFILE Education: Graduate in Labour Relations/ Master en HR. Languages: Spanish and English. French is a plus. Professional experience & know how: • Minimum 1 year of experience as a Management Assistant and/or in Human Resources, or in a related field., • Results-driven mindset., • Strong ability to organize and prioritize., • Good communication skills., • Ability to multitask., • Strong interest in the Luxury / Wines & Spirits industry., • Strong analytical skills., • Proficiency in Excel. Moët Hennessy is proud to promote a diverse, equitable and inclusive working environment for all.

At Rob Surgical we are looking to hire a Process Engineering Quality Assurance Technician to join our Quality team and support the continuous improvement and validation of our manufacturing and quality processes. 🧬 About us We are a healthtech company specialized in the development of advanced robotic systems for high-precision minimally invasive surgery. Founded in 2012 as a spin-off from UPC and IBEC, our mission is clear: to make robot-assisted surgery more accessible, precise, and efficient worldwide. 🔍 What will your mission be? As a Process Engineering QA Technician, you will play a key role in ensuring the effectiveness of our Quality Management System (QMS) by supporting the validation master plan, calibration program, and process quality activities. You will work closely with product managers, project managers, developers, and manufacturing teams to ensure quality and regulatory compliance across the entire product lifecycle. 🛠 Your main responsibilities will include: Quality Management System • Drafting and reviewing documentation related to QMS processes., • Participating in the maintenance of risk analyses for QMS processes., • Monitoring and maintaining quality KPIs., • Conducting regular inspections in the production plant to verify process control and compliance with procedures., • Organizing and participating in quality meetings., • Supporting the transfer from design to production, including control plans and control methods., • Training manufacturing personnel when required., • Supporting the design and construction of test rigs for design and manufacturing validation., • Writing validation protocols and reports., • Participating in validation execution and monitoring progress of the validation plan., • Preparing validation maintenance reports and monitoring equipment, facilities, and services., • Participating in validations related to:, • Clean rooms, • Ethylene oxide and wet steam sterilization systems, • Computerized systems, • Analytical test methods, • Maintaining and updating facility and process risk analyses., • Monitoring the calibration program and reporting progress., • Developing and updating calibration procedures., • Participating in calibration activities and issuing calibration reports., • Supporting internal and external audits., • Collaborating in the preparation of annual R&D reports and department budgets., • Supporting administrative tasks related to documentation, digitalization, and archiving., • Contributing to maintaining an organized and efficient work environment. 🎓 What are we looking for? • Bachelor’s degree in Industrial Engineering is highly valued., • Experience level: 3+ years of experience, • Experience in medical devices and/or pharmaceutical industry is highly valued., • Professional working proficiency in English., • Advanced Microsoft Office user., • Experience working with ERP environments. 📚 Valuable knowledge Experience or training related to: • ISO 17025 – Calibration laboratories, • ISO 14644 – Clean rooms, • ISO 11135 / ISO 14937 – Sterilization of medical devices, • ISO 14971 – Risk management for medical devices, • GAMP5 – Validation of computerized systems, • GMP and validation regulations, • Metrology or microbiology 💡 We are looking for someone who is… • Detail-oriented but able to understand the big picture., • Analytical, proactive, and collaborative., • Meticulous, organized, and efficient., • A strong communicator with teamwork. 🎯 What do we offer? • Full-time permanent contract., • Salary aligned with profile and experience., • Flexible working hours., • Monthly fruit and vegetable box 🍎, • Opportunity to work on cutting-edge surgical robotics technology., • Professional development in a highly innovative and regulated environment., • A dynamic and collaborative team where your work has real impact on patients’ lives.

Contrato laboral formativo para la obtención de la práctica profesional con una duración de 12 meses. Imprescindible tener titulo universitario obtenido en los últimos 3 años. As an HR Intern, your main mission will be to support the HR function in Iberia with administrative tasks as well as recruitment activities, in close cooperation with our HR Business Partner. You will also support our Managing Director with administrative tasks. RESPONSIBILITIES OF THE ROLE HR administration: • Support Human Resources with the processing of employee payroll, update the payroll database with changes, and maintain payroll files., • Support employees throughout the employee lifecycle (including onboarding and offboarding administration, preparation of HR-related documents, master data maintenance in the HR tool, and maintaining complete employee files in compliance with GDPR); provide ad hoc support as needed., • Support Human Resources in the digitalization of personnel files (PeopleDoc project)., • Support global Human Resources projects and take ownership of small projects independently., • Raise purchase orders and record invoices against budgets., • Support the recruitment process., • Keep up to date the public HR SharePoint for all the employees. Managing Director Assistant • Coordinate agendas and plan the monthly Managing Committee meetings., • Send Outlook invitations for the monthly “MH Iberia Call” virtual meeting and follow up by email to collect the topics to be shared., • Support the administrative organization of Market Visits: travel and transfer arrangements, hotel bookings, and invoice/payment management., • Organize trips to Maisons for VIP customers: planning, travel arrangements, budgeting, supplier management, and logistics. PROFILE Education: Graduate in Labour Relations/ Master en HR. Languages: Spanish and English. French is a plus. Professional experience & know how: • Minimum 1 year of experience as a Management Assistant and/or in Human Resources, or in a related field., • Results-driven mindset., • Strong ability to organize and prioritize., • Good communication skills., • Ability to multitask., • Strong interest in the Luxury / Wines & Spirits industry., • Strong analytical skills., • Proficiency in Excel. Moët Hennessy is proud to promote a diverse, equitable and inclusive working environment for all.

Amaris is looking for a Data Manager with strong experience in clinical data management for CRO environments. The position focuses on supervising data management activities to ensure the smooth progress and quality of clinical projects. 🔥 Your Responsibilities • Act as the main point of contact for all data management topics and participate in project/study meetings, • Contribute to the selection of subcontractors by preparing specifications and evaluating proposals, • Participate in study design, including data management sections in protocols and CRF specifications, • Oversee outsourced data management activities, ensuring compliance with cost, timelines, and data quality, • Validate deliverables such as data management plans, validation plans, transfer specifications, eCRF completion guides, and coding instructions, • Test eCRF before production deployment and after each protocol amendment, • Implement targeted quality control of data based on risk assessment, • Monitor progress of data management steps (entry, cleaning, coding, external data transfers, SAE reconciliation, etc.), • Approve SDTM specifications and verify SDTM packages as needed, • Regularly assess subcontractor service quality, establish action plans for deviations, and discuss corrective measures, • Participate in data review meetings and validate associated reports, • Ensure responsibility for database lock and unlock, verifying all prerequisites, • Provide statisticians with data for statistical analysis, • Verify the presence of all data management documentation in the Trial Master File (TMF) 🎯 Your Qualifications • Experience in clinical data management for CROs (5–10 years), • Proficiency with industry-standard data management tools and software, • Academic background in Life Sciences, Pharmacy, or related field, • English fluent. French is a plus., • You demonstrate strong analytical and problem-solving skills, • You demonstrate excellent communication skills 💡 What You’ll Get From Us • An international community bringing together 110+ different nationalities, • An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities, • A robust training system with our internal Academy and 250+ available modules, • A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.), • At Mantu, sustainability is part of everything we do. You’ll have the opportunity to turn your ideas into action and make a tangible impact. Every day, our teams bring our ESG commitments to life, from reducing our footprint to driving positive change within our communities. Through our WeCare Together program, you’ll be empowered to design and lead projects that create real social or environmental impact, with the company’s full support. Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

AUTSORSA is a fast-growing company founded and based in Bulgaria that serves clients from all over the world, providing business outsourcing, outstaffing and HR services. Our client is a leading European semiconductor company developing cutting-edge AI chip infrastructure. They are at the forefront of memory subsystem design and high-performance computing, creating innovative solutions that power the next generation of AI processors. If you are passionate about microprocessor architecture and top-level design — and want to contribute to projects that redefine the boundaries of AI hardware — this is the perfect opportunity to join a fast-paced, innovative environment where your expertise will make a real impact. We are looking for a Senior Verification Engineer to join a highly skilled team developing next-generation AI hardware. As a Senior Verification Engineer, you will be part of our Verification Team and take on a key responsibility: ensuring that complex digital designs behave exactly as intended at the Register Transfer Level. Develop and maintain UVM-based verification environments for complex digital designs. Create test plans, define verification strategies, and ensure full functional and code coverage. Build SystemVerilog testbench components and automate regressions using Python, Perl, Bash or TCL. Track verification progress using coverage metrics and deliver high-quality results on schedule. Master’s degree or PhD ~ English level C1 ~Experience with scripting languages (Python, Perl, Bash, TCL) and regression frameworks ~ Familiarity with version control systems (git, svn) ~ Relocation package for you and your family (visa, flight, first month rent, housing assistance). Permanent, full-time onsite role in Barcelona, Spain . Flexible working hours (9–6, Monday to Friday). Work in one of the very few companies in Europe building AI chip infrastructure . Small, highly skilled team (147 people ) with opportunities for learning and growth. Supportive, family-friendly environment with strong relocation assistance. Candies, coffee, and free Spanish lessons included! &##By applying to this advertisement, you voluntarily provide your personal data and consent to their processing for the purposes of recruitment. The processing of your personal data is carried out in full compliance with the requirements of Regulation (EU) 2016/679 (General Data Protection Regulation), the Personal Data Protection Act, and all other applicable regulations.

Protekting was founded in 2014 in Barcelona.The company started as a trading company for phytosanitary products, and quickly opened to all kind of agriculture solutions. We are focused on products and services that help our clients protect and grow crops efficiently. We are strongly committed to our clients’ needs as well as to the responsible use of products for agriculture. Although we are a young team, we have a lot of experience in the world of plant protection. We are flexible, innovative, passionate and focused on protekting our clients and partners’ interests, by helping them to grow their business. Here’s the lowdown on what your role will actually look like (spoiler alert: it’s awesome!) We are seeking for Laboratory Analyst to join our Team. What you'll be rocking: • Analysis of samples from all stage of the development process., • Responsible for the reporting of data., • Collaborate in the transfer of analytical methods., • Collaborate in development and validation of new analytical methods for active phytosanitary ingredients and finished formulated products., • Collaborate in the analysis and evaluation of the developing products for dossier submission., • Maintain all records in compliance with SOPs and Policies., • Writing technical reports and Standard Operating Procedures (protocols, specifications and reports). Preparation of SOP’s for General Laboratory. Practice and Laboratory Instruments., • Management and collaboration in general tasks of laboratory (equipments, standards, control of stocks..) What you bring to the table: • Basic laboratory skills and research experience of most of the following analytical techniques: HPLC, UV, UPLC, LC-MS, GC-MS, PSD, potentiometric titration, KF titration andIR., • Knowledge of analytical method transfers., • Experience MS Office. Educational milestone: • Degree in life sciences., • Qualified in Analytical Development., • Excellent level of English and Spanish, spoken and written. Your key superpowers: • Self-sufficient., • Strong analytical skills and problem solving., • Highly responsible and capable to work under pressure to meet deadlines., • Ability to prioritize multiple tasks., • Good team player., • Strong organizational, planning and time management skills, to archive project timelines., • Detail oriented and good communication and research skills., • Motivated, proactive, dynamic, methodical, organized and decisive. We’re looking for someone who works hard, plays hard, and laughs harder. Sound like you? Come aboard. Believe in life

We are seeking a Deployment Engineer to support complex gateway deployment operations and ensure a seamless transition from construction to live network operations. This role plays a critical part in delivering operational excellence across international telecommunications infrastructure projects. The successful candidate will combine technical understanding with strong coordination and documentation capabilities. About the Role You will manage deployment documentation, coordinate multidisciplinary technical activities, oversee schedules, and ensure full operational readiness prior to service activation. Acting as a bridge between construction, RF engineering, network operations centers (NOC), and field services teams, you will ensure infrastructure is delivered on time, compliant, and ready for integration into live service environments. Responsibilities Documentation & Acceptance Readiness Prepare comprehensive acceptance packages including technical specifications, test results, and compliance documentation Maintain accurate documentation throughout the deployment lifecycle Coordinate configuration validation and acceptance testing activities Ensure regulatory, safety, and technical prerequisites are completed for timely activation Technical Coordination & Deployment Tracking Track critical technical tasks and identify schedule risks or resource conflicts Coordinate across engineering, construction, NOC, and field services teams Provide milestone reporting and manage escalations Align technical execution with project timelines and delivery baselines Operational Handover & Transition Validate completion of commissioning activities before operational handover Confirm readiness for service activation and monitoring integration Prepare operational procedures, maintenance schedules, and technical references Support structured knowledge transfer to operational support teams Quality Assurance & Process Improvement Monitor compliance with deployment and change management procedures Identify documentation or process gaps and support continuous improvement initiatives Assist in developing standardized templates and delivery frameworks Participate in post-deployment reviews and implement lessons learned Qualifications Bachelor’s degree in Engineering, Telecommunications, IT, or related technical field Associate degree with relevant experience considered Required Skills Minimum 2+ years in service delivery, network deployment, or technical project coordination Experience within telecommunications or connectivity infrastructure environments Strong background in documentation control and cross-functional coordination Spanish and English Professional Proficiency is a must. Preferred Skills Understanding of deployment processes and gateway infrastructure systems Experience with change management and acceptance testing workflows Familiarity with configuration management and documentation control systems Knowledge of service handover and operational transition processes Pay range and compensation package Location: Based in Spain or the UK. Work authorization required. Flexibility expected for working hours to coordinate with global teams. Occasional off-hours or weekend availability during activation or transition phases. Occasional travel required for key deployment milestones. Equal Opportunity Statement We are committed to diversity and inclusivity.

As part of the Strategic Initiative , ICFO coordinates PIXEurope, a flagship Pilot Line funded under the European Chips JU program . With €400 million in investments and a consortium of 20 partners across 11 countries, the project aims to reinforce Europe's strategic autonomy in photonic technologies and accelerate industrial uptake of cutting-edge integrated photonics. Over the next decade, PIXEurope will enable the transfer of advanced technologies to manufacturing environments, while fostering innovation and scalability across the European photonics ecosystem. ¿Es este el puesto que está buscando? Si es así, siga leyendo para obtener más detalles y no olvide enviar su solicitud hoy mismo. PIXEurope will involve the establishment of a gateway for easy access to the Pilot Line services. This involves generation of large data sets, including those related to the development, setting up, material supply, equipment procurement, use and maintenance, processes, design kits, open access and services, such as collaborative projects, training, and prototyping, and financial execution. The creation and operation of a data platform that is effective and easy to use by Pilot Line partners as well as external end-users is critical for the success of the initiative. POSITION OVERVIEW We are seeking a Pilot Line Data and Gateway Officer with a solid background in IT/software engineering or related fields to support the procurement, setting up, operational deployment and open access phases of the PIXEurope Pilot Line. The selected candidate will be responsible for developing, configuring, and maintaining the software tools and interfaces that enable efficient and compliant data management. Working in close coordination with the Pilot Line Director, Pilot Line Financial and Procurement Manager, Pilot Line Open Access Manager, Pilot Line Installation and Acceptance Manager, Pilot Line Training and Interoperability Manager, The Pilot Line Data and Gateway Officer will also act as a liaison with the data management teams of partner institutions to harmonize procedures and maximize operational efficiency. The role requires proven data management, knowledge of software interfaces for handling of large data sets, strong command of data management compliance, and excellent coordination skills across multi-partner environments. KEY RESPONSIBILITIES • Support the Pilot Line Director and Managers in the creation and operation of the Data Platform and Gateway., • Support the Pilot Line in all data management operation., • Contribute to the development and monitoring of data management systems for the Pilot Line, • Ensure software interfaces meet the requirements of the Pilot Line’s activities, particularly for Joint Procurement (JP) and Open Access/Operation (DEP)., • Liaise with ICFO’s IT and administrative teams to ensure compliance with institutional policies and with data management requirements from Chips JU and national co-financing bodies., • Coordinate with data teams at partner institutions to harmonize tools, share resources, and promote interoperability., • A university degree in data management, IT, software engineering or related fields., • Proven experience in the development or administration of software platforms for technical or scientific environments, • Strong knowledge of software interfaces and database management, • Demonstrated understanding of data protection, traceability, and compliance frameworks, • Fluency in English and Spanish (written and spoken)., • Excellent coordination and interpersonal skills, with a service-oriented mindset., • Strong organizational skills, attention to detail, and ability to meet deadlines autonomously., • Indefinite contract for scientific and technical activities pursuant to Spanish Law 14/2011, linked to the duration or availability of funds within the PIXEurope Pilot Line, • A collaborative and interdisciplinary environment at the interface of academia, industry, and innovation., • A competitive salary according to ICFO’s internal scales and a family allowance, if applicable, in line with institutional policy. Applications should be submitted via LinkedIn or the ICFOjobs platform: Required application materials: • A presentation letter outlining your interest in the position. ICFO is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. For formal enquiries regarding the application process, please contact: For project and technology enquiries, please contact: For more information about ICFO, visit: PIXEurope is co-funded by the Chips Joint Undertaking and national funding authorities of the Participating States, Spain, Ireland, The Netherlands, Finland, Belgium, Portugal, Poland, Austria , France, Italy, United Kingdom. xcskxlj In particular, it is co-funded by Spain through the Ministry for Digital Transformation and Civil Service under reference CJU- , as part of the Recovery, Transformation and Resilience Plan (PRTR).

Hybrid 50%. Our client is a science-led ingredients manufacturer entering an exciting new stage of commercial expansion. We are seeking a Client Acquisition Executive to identify, prospect, and qualify new business opportunities that will support continued global growth. In this position, you will be responsible for generating new leads and creating a consistent flow of qualified business opportunities across international markets. Conduct proactive commercial outreach through calls, emails, and networking activities. Qualify new leads and transfer them to Inside Sales and Sales Managers. Build and manage a structured sales pipeline, tracking progress against KPIs and timelines. Collaborate closely with Inside Sales, Sales Managers, and Marketing to ensure strong lead conversion. Previous experience in business development, inside sales, or sales prospecting. Communication skills in both Spanish and English. This is an excellent opportunity for a motivated sales professional who is eager to grow their career in international sales with an innovative & growing company.

R&D Manager - Medical Devices (High‐Risk Class III) - Freelance (6 Months)Location: Barcelona, Spain (On‐Site)Contract: 6‐month freelance contract with the possibility of a permanent offerIndustry: High‐Risk Medical Devices Inscríbase ahora, lea los detalles del trabajo desplazándose hacia abajo. Verifique que posee las habilidades necesarias antes de enviar una solicitud. About the Role We are seeking an experienced R&D Manager to lead the development of high‐risk Class III medical devices-specifically balloon catheters, vascular stents, or comparable interventional products . You will manage a multidisciplinary team of engineers and drive projects from early‐stage feasibility through design, verification, qualification, and transfer to manufacturing.Spanish language skills are not required . Full‐time on‐site presence in Barcelona is essential. Key Responsibilities R&D Leadership & Team ManagementLead and mentor a team of R&D engineers , providing technical direction, workload prioritization, and performance development.Oversee daily engineering activities including design iterations, prototyping, test planning, and documentation.Establish and enforce robust engineering processes aligned with global regulatory expectations. Design & Development of High‐Risk DevicesOwn the full design life cycle , from concept development and feasibility testing through to final design freeze.Drive detailed engineering work for balloon catheters, stents, or similar interventional devices , including:Balloon forming and bonding processesStent design, coatings, and mechanical performanceCatheter shaft architecture and material selectionTolerance analysis, DFM/A, material characterisationLead Verification & Validation (V&V) strategy, including test method development, equipment qualification, and protocol/report generation. Qualification & IndustrialisationManage design qualification , including performance testing, biocompatibility considerations, sterilisation validation input, and packaging qualification.Oversee transfer of designs into manufacturing / scale‐up , collaborating with process engineering and suppliers. Project & Stakeholder ManagementAct as project owner for multiple R&D programmes, managing timelines, budgets, risk registers, and resource allocation.Coordinate with Quality, Regulatory, Clinical, and Operations teams to ensure coherent project execution.Present project updates to leadership, aligning on strategy, risks, and technical decisions. Regulatory & Compliance (FDA and MDR)Ensure all R&D activities adhere to Design Control requirements under 21 CFR 820 and EU MDR .Lead or contribute to core regulatorydeliverables, including:Design History File (DHF)Risk Management File (ISO 14971)Design Inputs/OutputsVerification/Validation documentationSupport regulatory submissions through technical report preparation and cross‐functional input. Required ExperienceMinimum 3 years' experience in R&D management within the medical device sector.Proven hands‐on experience with high‐risk Class III devices , preferably balloon catheters or stents .Demonstrated ability to lead engineering teams and manage complex technical projects.Strong understanding of Design Controls , Risk Management , V&V , and qualification activities.Proficiency with FDA 21 CFR 820 , EU MDR , ISO 13485, and ISO 14971.Excellent organisational and communication skills. xcskxlj Ability to work full‐time on site in Barcelona.

About the Company ECCBC (Equatorial Coca‑Cola Bottling Company) is a leading Coca‑Cola bottler operating across North and West Africa. With more than 30 years of presence in the region, we produce and distribute some of the world’s most iconic beverages while supporting local economies, developing talent, and fostering sustainable growth. Our mission is to refresh our communities and make a positive impact through responsible operations, innovative digital transformation, and a strong people‑focused culture. Across our markets, we are committed to excellence, operational efficiency, and continuous improvement in everything we do. Joining ECCBC means becoming part of a dynamic, multicultural environment where collaboration, growth, and innovation drive our success. JOB MISSION The Data Technical Lead ensures the successful technical design, implementation, and quality assurance of data solutions within a specific business domain. This role bridges enterprise data architecture and operational delivery, ensuring that data initiatives are well‑designed, properly implemented, scalable, and aligned with business needs. The Data Technical Lead is responsible for the technical design, implementation, and quality control of data solutions within the domain, including the evolution of the Data Lake built on Medallion architecture principles. KEY RESPONSABILITIES • Architecture & Design: Lead technical design of data solutions on Azure / Microsoft Fabric, defining Medallion architecture (Bronze / Silver / Gold), Spark processing patterns, and scalable SQL data models aligned with enterprise architecture., • Data Governance Enablement: Ensure data governance standards through architectural alignment, Medallion design, and robust technical frameworks., • Platform & Tools: Oversee implementation of data pipelines using Spark and SQL, manage Lakehouse structures, optimize performance, and ensure integration with legacy tools (SSIS, cubes)., • Data Quality & Controls: Define and monitor data quality metrics, ensure compliance (e.g., SOX), and validate consistency of data ingested from SAP S/4HANA and other ERP systems., • Continuous Improvement: Identify architectural and process improvements to enhance performance, scalability, and cost efficiency of the Fabric platform., • Technical Leadership & Vendor Oversight: Review code (Spark, SQL), validate technical design decisions, supervise external vendors, and ensure sustainable knowledge transfer., • Guidance: Drive compliance with established standards and metrics; communicate and enforce data policies, rules, and governance requirements. EDUCATIONAL AND SPECIFIC TRAINING REQUIREMENTS • Bachelor’s Degree in any discipline, • English proficiency required; medium French level valuable, • Senior expertise in Azure cloud data platforms and modern architectures (Microsoft Fabric, Data Lake, Medallion), • Strong hands‑on experience with SQL, Power BI, SSIS, and multidimensional/tabular models (cubes), • Ability to work across modern cloud environments and legacy BI ecosystems, • Solid understanding of ERP systems (SAP MM, MRP, SD) and enterprise data flows, • Ability to translate business requirements into robust technical solutions while balancing priorities and constraints, • Strong credibility with senior stakeholders; ability to lead and coordinate external vendors, • FMCG industry experience is a plus AREAS OF EXPERTISE & YEARS OF EXPERIENCE (Short Version) • 7–10 years of experience in Data Engineering, BI, or Data Architecture, • Strong hands-on experience with Azure data platforms (Fabric, Data Lake, Medallion), • Advanced skills in SQL, Spark, Power BI, SSIS, and tabular/multidimensional models, • Experience working with ERP data, especially SAP (MM, MRP, SD), • Proven technical leadership and vendor coordination, • Experience in FMCG environments is a plus PERFORMANCE INDICATORS • Demonstrated senior expertise in Azure data platforms, Microsoft Fabric, Data Lake, and Medallion architecture, • Proven experience delivering large‑scale data platforms using Spark and advanced SQL, • Strong hands‑on capability with Power BI, SSIS, and multidimensional/tabular models, • Ability to integrate cloud and legacy BI ecosystems effectively, • Strong understanding of SAP (MM, MRP, SD) data flows, • Technical leadership translating business needs into scalable solutions, • Effective coordination and oversight of external vendors MAIN COMPETENCIES (ECCBC Competencies) • Drive for Results, • Cross‑Cultural Mindset, • Engagement, • Strategic Thinking, • Leadership for Change, • Teamwork FUNCTIONAL & TECHNICAL COMPETENCIES • Understanding of existing technology architecture, • Ability to assess data‑related changes for technological impact, • Knowledge of business rules used to populate data, • Strong process mindset and excellent root cause analysis, • Experience with metrics gathering, tracking, and reporting Percentage of Travel Required • Around 20% Internal Departments Interaction • HQ Employees and HQ Managers, • Country Managers, • Department Heads in Countries External (Customers / Vendors) Interactions • Providers, • Third‑party customers, • Offshore customers

pstrongTax Advisor (Center of Excellence) /strong /ppbr/ppWe are looking for a Tax Advisor to work in a multinational company. Its products and services are designed to benefit people and improve their quality of life. /ppbr/ppstrongPURPOSE /strong /ppWithin our one Tax Community and our Operating Model for Taxes at the company, the Global Business Services (GBS) team plays a key role performing international and local tax activities regarding Tax Compliance (including Indirect Direct taxes), Tax Accounting and Transfer Pricing, and provides tax advice within the GBS community and contributes to continuous process improvements. /ppAs part of the organization within the GBS community, we have a Tax Center of Excellence (CoE) team all around the different locations that encompasses different process areas as Tax Compliance, Tax Accounting, Transfer Pricing, Tax Technology and Digital Transformation. /ppThe main activities and responsibilities of this team are giving tax advise within the GBS team and be key contact to headquarters and local teams; caretaking for outsourcing; managing complex tax activities within the region under scope and/or with global impact, including tax audit support; continuous process improvements (cross-functional alignments, automation data analytics); support to Global Process Owner (GPO)’s projects; knowledge management; give advice on tax reporting activities; etc. /ppThe team acts as the counterpart of the respective GPOs, both putting the global standards/settings into operations and providing the feedback, ideas, and operational knowledge from the operations. /ppFor our Global CoE Tax team, we are looking for a CoE Tax Advisor who provides support and advice regarding Direct tax (including Corporate Income Tax (CIT) topics, Withholding Tax Accounting and Tax Reporting) and Indirect tax (VAT, Intrastat, EU Sales Tax, etc.) for some of the countries where the Group has its presence. /ppbr/ppstrongYOUR TASKS AND RESPONSIBILITIES /strong /ppThe successful candidate will: /pp• Provide tax advice for indirect and direct tax topics to the tax teams within GBS. /pp• Manage complex tax activities within region and/or with global impact, including Tax Audit support steering. /pp• Quality gate activities: /pp• Risk based random review of tax declarations. /pp• Approval of most relevant tax payments. /pp• Review tax declarations for complex legal entities and complex issues. /pp• Perform / organize trainings to further increase tax specific knowledge. /pp• Define additional data checks and coordinate with GPO. /pp• Caretaker for outsourcing and first point of contact. /pp• Participation and leading role in transition projects /ppbr/ppstrongWHO YOU ARE /strong /pp• BA/BS degree in Tax/Fiscal, Finance, Accounting, Law or Business with 4+ years of experience in tax advisory or in a multinational company. /pp• Strong capabilities to work through ambiguity and for sound judgment. /pp• Advanced ability to work through ambiguity. /pp• Advanced level of capability to understand complexity of changes with respect to business and regulatory environment and to respond quickly. /pp• Advanced level of capabilities to lead change, projects, and initiatives. /pp• Advanced level of capability to collaborate. /pp• Advanced level of ability to explain the "why", ability to influence people and to drive change or to execute governance of Tax. /pp• Strong tax judgment and business knowledge or ability to quickly learn. /pp• Advanced level of capability to collaborate task/project oriented without geographical, organizational, or functional boarders. /pp• SAP experience is a plus. /pp• Very good analytical skills and the proactive attitude to drive process changes. /pp• Customer oriented mind-set, change management capabilities and Team player. /pp• Competence to grasp an overview of complex subjects and deduce operational activities. /pp• Exceptional interpersonal communication, and presentation skills and ability to manage multiple and diverse stakeholders. /pp• A high proficiency level in English, both written and spoken complete your profile /p

At Rob Surgical we are looking to hire a Development Engineer to join our R&D team. &##We are a healthtech company specialized in the development of advanced robotic systems for high-precision minimally invasive surgery. Founded in 2012 as a spin-off from UPC and IBEC, our mission is clear: to make robot-assisted surgery more accessible, precise, and efficient worldwide. &##As a Development Engineer, you will play a key role in the design, development, and optimization of our computer-controlled surgical robotic systems, endoscopic instruments, and accessories. You will contribute to the full development lifecycle (from concept and design to verification, industrialization, and transfer to production) ensuring compliance with regulatory and quality standards within the medical device industry. &##Design and development of computer-controlled surgical systems, endoscopic instruments, and accessories, including optimization of designs and subsystems. Design and execution of test benches and specific experiments, including drafting and review of protocols and test reports. Preparation, review, and maintenance of design and development documentation and technical files. Coordination with production and suppliers, including support in design transfer, component/process requirements, and training of production personnel. Support in administrative and technical documentation tasks to ensure compliance with Quality Management System requirements. &##Degree in Industrial Engineering, preferably specialized in Robotics or Mechatronics. Experience in the medical device industry. Engineering background with exposure to mechanical, electronic, and software design (preferred). &##Strong organizational and planning skills. Fluent English (B2–C1). &##Full-time permanent contract. Flexible working hours. Professional development within a highly innovative and regulated environment.

About Us HBX Group is the world’s leading travel technology partner, connecting hotels, tour operators, and travel sellers across 140+ markets. With a network of 300,000 hotels and 60,000 travel distributors, we help partners grow through innovative, data‑driven distribution and visibility solutions. Our teams combine technology, insight, and local expertise to deliver impact across the global travel ecosystem. Role Overview We are seeking a commercially driven Regional Supplier Sales Manager – Marketing Solutions to sell HBX’s portfolio of marketing and visibility products to hotels, hotel chains, tour operators, and transfer providers. Although based within the Marketing department, this role is sales‑focused . You will engage suppliers across the Middle East, Asia, and the Pacific, understand their visibility and traffic goals, scope budgets, and design tailored promotional packages that elevate their presence across HBX channels. You can be based in Spain or APAC , covering a wide regional scope. Key Responsibilities • Build and grow relationships with hotels, chains, tour operators, and transfer providers across ME → APAC., • Conduct discovery conversations to understand visibility needs, market challenges, seasonality, and commercial goals., • Translate supplier needs into clear promotional objectives and recommend HBX marketing solutions to meet them., • Own the full sales cycle: prospecting, pitching, budgeting, contracting, and closing., • Negotiate budgets, set pricing, and build tailor‑made promo packages that drive measurable visibility and revenue for suppliers., • Create customised marketing proposals using HBX’s portfolio (display, sponsored placements, campaign bundles, branding solutions, etc.)., • Advise partners on which marketing levers best amplify demand based on their strategy and target markets., • Ensure campaigns are accurately briefed to internal operational and marketing teams for smooth delivery., • Manage and grow a book of business across ME → APAC, consistently hitting revenue and growth targets., • Monitor performance of live campaigns and share results, insights, and optimisation recommendations with suppliers., • Use data and reporting tools to identify upsell, renewal, and expansion opportunities., • Partner closely with regional commercial teams, product, and marketing operations to align on priorities and customer needs., • Provide voice‑of‑customer insights to improve HBX marketing products and drive adoption., • Ensure all partners receive a premium, consultative experience. Skills & Experience • Proven commercial or sales experience, ideally selling media, marketing, advertising, or visibility solutions to hotels or travel suppliers., • Strong understanding of travel distribution , including hotels, OTAs, wholesalers, tour operators, and channel dynamics., • Ability to uncover customer needs, translate them into commercial opportunities, and build tailored proposals., • Confident negotiator with experience managing budgets and closing deals., • Strong relationship builder with excellent communication and presentation skills., • Data‑savvy, able to discuss performance metrics and campaign results clearly., • Highly organised, proactive, and comfortable managing a multi‑market scope., • Fluent English; other regional languages are a plus. We believe diversity drives innovation and supports our mission to make travel a force for good. HBX Group is committed to creating an inclusive, equitable environment where every individual can thrive.

About the Role We’re seeking an experienced Senior ERP Data Migration Specialist to lead a high-impact data migration initiative from NetSuite to SAP S/4HANA , with a particular emphasis on the SAP S/4HANA Retail module. This role is mission-critical for ensuring data integrity, minimal disruption to business operations, and successful transition to SAP's next-generation ERP system. If you have a strong track record of large-scale ERP migrations, especially involving SAP S/4HANA, and hands-on expertise with SAP’s migration tools, this is an excellent opportunity to bring that experience to a strategically important project. Key Responsibilities • Lead the end-to-end data migration from NetSuite to SAP S/4HANA , including planning, scoping, mapping, transformation, validation, and reconciliation., • Collaborate with business stakeholders, SAP functional leads, and technical teams to understand legacy data structures and ensure alignment with SAP S/4HANA Retail requirements., • Utilize SAP S/4HANA Migration Cockpit (LTMC) and Migration Object Modeler (LTMOM) for building and managing data migration objects., • Design and document data migration strategies, timelines, data cleansing approaches, and cutover plans., • Monitor and troubleshoot data migration issues, ensuring data quality, consistency, and auditability., • Provide knowledge transfer and training to internal teams regarding best practices in SAP S/4HANA data migration., • Support data validation activities including mock loads, dry runs, and go-live cutover execution. Required Qualifications • 5+ years of ERP data migration experience , with direct experience migrating from NetSuite to SAP S/4HANA strongly preferred. If not direct, must have deep experience with other ERP-to-SAP S/4HANA migrations., • Proven expertise with SAP S/4HANA Retail data structures and business processes., • Direct experience with SAP Public Cloud., • Strong hands-on experience using SAP S/4HANA Migration Cockpit (LTMC) and Legacy Transfer Migration Object Modeler (LTMOM) ., • Solid understanding of data mapping, cleansing, transformation, and reconciliation processes., • Excellent collaboration and communication skills, with the ability to work across functional and technical teams in a global environment., • Strong documentation, QA, and problem-solving skills related to data migration. Preferred Qualifications • Experience with large-scale global SAP implementations ., • Familiarity with NetSuite data structures and export methodologies., • Prior experience in retail, wholesale, or consumer products industries., • SAP S/4HANA certification is a plus. Join Our Global Team: We invite you to apply for the position at RE Partners. Join us in shaping the future of business technology consulting and transforming the way organizations thrive in a digital world. As a diverse, woman-owned global business, we pride ourselves on keeping talent happy – our 7% attrition rate speaks volumes. Bring your talented friends along and earn a referral bonus Equal Opportunity Employer: We are an equal opportunity employer and welcome applications from all qualified individuals regardless of race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, or veteran status.

At Gracia101 , we're seeking a Senior SAP MM-LE-WM Consultant to join the team. This is a Freelance and remote role, the role involves participating in projects and new implementations for a global company, supporting delivery across the full project lifecycle. Key Responsibilities Participate in SAP logistics projects and new implementations. Gather requirements and contribute to process design. Configure SAP MM, LE, and WM modules. Support testing, UAT, and knowledge transfer (KT). Handle Idocs and interfaces, including specifications, testing, processing, and error handling. Debug issues and provide solutions. Skills Needed Senior experience in SAP MM, LE, and WM. Expert in WM SAP standard. Hands-on experience with Idocs and interfaces. Proactive and solution-oriented. Good documentation and communication skills. High level of English to work with a global team. #J-18808-Ljbffr

Unique opportunity to work at the forefront of European photonics innovation, contributing to large-scale initiatives that shape the future of photonic integrated circuits Hands-on experience in managing complex, multi-partner projects while developing expertise in technology transfer, innovation ma

Unique opportunity to work at the forefront of European photonics innovation, contributing to large-scale initiatives that shape the future of photonic integrated circuits Hands-on experience in managing complex, multi-partner projects while developing expertise in technology transfer, innovation ma

Unique opportunity to work at the forefront of European photonics innovation, contributing to large-scale initiatives that shape the future of photonic integrated circuits Hands-on experience in managing complex, multi-partner projects while developing expertise in technology transfer, innovation ma

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The role involves responsibilities such as pilot plant supply, training in technical transfers, and preparing samples for analysis.

A leading services supplier in Barcelona is looking for a Technical Transfer Manager (NPI) to lead technology transfer execution for new product introductions. Responsibilities include cross-functional coordination and ensuring successful technology transfer, with on-site work required during shifts

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Support product launches from the new site following transfer in cooperation with Commercial Transfer Team, Supply Chain, QA, RA. Manager Global Technology Transfer is responsible for leading end-to-end Technology Transfer execution providing Project Management, scientific and technical expertise, e