Trabajos quality en Vallcarca - Page 18Crear alertas

As Group SARIA , we create value for our partners and the environment by acting as a reliable service provider and manufacturer of quality products for the agricultural, energy, animal feed, food, catering and pharmaceutical industries.Our wide portfolio of products and services is based on the tran

As Group SARIA, we create value for our partners and the environment by acting as a reliable service provider and manufacturer of quality products for the agricultural, energy, animal feed, food, catering and pharmaceutical industries. Our wide portfolio of products and services is based on the transformation of animal by-products and organic waste into high-quality raw materials for new applications, conserving the scarce existing natural resources and making, through our business model, an important contribution to environmental sustainability. Todos los candidatos deben asegurarse de leer atentamente la siguiente descripción del puesto y la información antes de enviar su solicitud. At SARIA, we are building a culture where everyone can feel at home, regardless of their gender, age, culture, sexual orientation, religion and disability. Together, we are successful as a global team. We want to foster innovation and empower our teams to share new ways of thinking, making the most of diverse talent. Our activities are characterised by entrepreneurial thinking combined with a high degree of local ownership. At the same time, as a family business, we value a hands-on mindset and want each employee to grow and develop their skills and career. It is this combination that sets us apart as an employer and characterizes life at SARIA. We are excited for you to become part of our team and fully join the adventure ahead. If you want to work with us and be part of our team as: Android Developer Tasks Maintain and improve Kotlin Android apps. Integrate native features: RFID SDKs, scanning, camera, biometrics, NFC, offline sync. Design simple UX for industrial and non-technical users. Apply strong security practices (OWASP, secure data, permissions). Ensure reliability: logs, crash reporting, analytics, performance. Develop automated tests and support CI/CD. Collaborate on REST/JSON APIs and OAuth2/OIDC. Document decisions, SDK integrations, release notes. Work closely with end users (operators/drivers) and iterate based on feedback. Requirements 2+ years of Android Kotlin experience. Experience with hardware/SDK integration (ideally RFID). Ability to design simple workflows for non-technical users. Knowledge of REST APIs, caching, offline-first patterns. Mobile security practices (OWASP). Fluency with Git-based workflows and CI/CD (e.g., Azure DevOps/GitHub Actions/Jenkins). Testing experience (unit/instrumentation/UI). Good communication skills in English; able to collaborate with cross-functional and distributed teams. Nice to Have (Valued) Experience with Angular, node.js and express framework for web applications Experience with Ionic + Capacitor for cross-platform mobile apps and packaging to Android/iOS. Basic Swift/Swift UI for iOS modules or Capacitor plugins. Knowledge of OAuth2/OIDC flows in device/browser contexts. Experience with App Distribution/MDM (Managed Play Store/Intune), app signing, and release processes. Observability in mobile (Firebase Crashlytics, App Center, App Insights) and feature flagging. Familiarity with Clean Architecture, MVVM, and dependency injection (Hilt/Koin). xcskxlj Exposure to integration platforms and message brokers (e.g., APIs managed via API Management; Kafka is a plus). Professional experiences At least 3 years experience

Novogene is a leading global provider of genomic services and solutions. Leveraging the latest next-generation sequencing (NGS), bioinformatics expertise, and the largest sequencing capacity in the world, Novogene provides unsurpassed data quality and fast turnaround time to all our customers. Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación. We are currently recruiting for a Logistics Specialist based in Spain. We’re searching for a proactive professional who can optimise workflows, manage vendor relationships, and ensure our goods move across the globe with precision. Location: Remote in Spain, ideally in major cities Job descriptions: 1. Customer Shipment Support a. Proactive Guidance: Provide clients with clear sample shipment instructions, including packaging standards, labeling requirements, and pickup scheduling procedures. b. Pickup Coordination: Schedule on-demand pickup services for clients, coordinating with logistics providers (e.g., DHL, FedEx, UPS) or internal Novogene drivers to collect sample packages at specified locations and times. c. Dedicated Point of Contact: Serve as the primary logistics liaison for clients during the shipment process, addressing all inquiries regarding transit times, tracking, customs clearance, and related matters. 2. End-to-End Shipment Monitoring & Issue Resolution a. Full Journey Tracking: Monitor real-time status of client shipments from pickup, transit, and customs clearance through to final delivery at the laboratory. b. Exception Management: Proactively identify issues such as shipping delays, customs holds, or missing documentation, and promptly coordinate with customs authorities, logistics providers, clearance agents, and internal teams for resolution. c. Client Communication Bridge: Provide transparent and timely updates to clients in case of logistics issues, effectively managing their expectations. 3. Compliance & Documentation a. Document Pre-review: Assist clients by reviewing or providing templates for required customs documents (e.g., commercial invoice, packing list, product description) prior to shipment to ensure accuracy and prevent clearance delays. b. Compliance Advisory: Ensure clients are aware of and adhere to relevant regulations for the international transport of biological samples. 4. Vendor Coordination & Process Optimization a. Daily Liaison: Maintain regular communication with contracted logistics providers to manage pickup appointments, service complaints, and optimize shipping solutions and costs. b. Feedback & Improvement: Gather logistics-related feedback from clients and internal teams, and contribute to the development and optimization of client shipment processes to enhance overall efficiency and customer satisfaction. 5. Other Duties a. Dry Ice Ordering: Arrange dry ice for client shipments as required. b. A limited amount of business travel is acceptable. c. Additional tasks as assigned by the direct manager. Your skills and experience: ● Education: College diploma or above. Preference for degrees in Logistics, International Trade, Life Sciences, or related fields. ● Experience: • Minimum 1 year of experience in international express/logistics customer service, operations, or a related role, with direct client communication and resolution of logistics issues., • Familiarity with basic import/export customs clearance procedures in key European countries (e.g., Spain, UK, Germany)., • Prior experience in the biological or related industry's logistics, with knowledge of sample transportation specifics, is preferred. ● Skills & Competencies: • Language: Fluency in both Spanish and English (written and spoken) is required. Knowledge of Chinese is a plus., • Excellent customer service orientation and communication skills: patient, clear, proactive, and able to explain logistics processes and handle issues in a client-friendly manner., • Strong problem-solving ability: capable of quick response under pressure and coordinating multiple resources to resolve in-transit issues., • Detail-oriented: high sensitivity to tracking numbers, client information, and document details., • Technical Skills: Proficiency in Microsoft Office; capable of data consolidation and analysis. Novogene is an Equal Opportunity Employer that prohibits discrimination and harassment of any kind. Novogene is committed to ensuring all qualified applicants will receive consideration for employment without regard to race, colour, religion or belief, sex, sexual orientation, gender identity, nationality, disability, or any other legally-protected characteristics. All employment decisions at Novogene are based on business requirements for its positions and skill sets of applicants. xcskxlj The business is committed to providing an inclusive and accessible recruiting experience for candidates with disabilities or other physical or mental conditions. Our privacy policy: _up*MQ..&gclid=Cj0KCQjwuMuRBhCJARIsAHXdnqOgH94fnKpCUZRAZBfyifMnPwPWW-i79qDY1FSjDWJGyhkLfYM7xU0aAgBiEALw_wcB

We are looking for a highly organized people & operations manager with a go-getter attitude to join our team in Barcelona. You’ll be working closely with the Accounting and HR consultants to manage invoices, payroll, recruitment processes to provide support to our creative & marketing teams on a daily basis. You will be responsible for running both our Barcelona and Berlin offi ces. You are a people’s person with great communication skills. ¿Está considerando presentar su candidatura para este trabajo? Compruebe todos los detalles en esta descripción del puesto y luego haga clic en "Solicitar". What we offer: ● Full-time position, fi x term contract, reporting to the Managing Partner ● Collaborative atmosphere, working together in an interdisciplinary team where you’ll support other teams and receive support from the management team ● Autonomy, you can work with little supervision at a good pace ● Regular feedback exchange, participate in company off-sites, and access to a professional L&D budget to spend on conferences, seminars, and workshops ● Home office once a week ● Career development opportunities What should you bring: ● A good understanding of the HR basics such employee management, payroll administration and expenses by reporting them to our external consultants ● As well as the Finance basics such uploading monthly expenditure and collect bills from vendors by reporting them to our consultants, as well as managing the invoicing workfl ows and payments ● Ideally ERP user-savvy to help with our company administration (finance system, employee portal) ● Good organisational skills to support on travel bookings and events ● Spanish-speaker, and good level of spoken and written English Responsibilities include: ● Company’s accounting and HR in collaboration with with our external consultants ● Manage monthly expense reports ● Booking travel and other ad hoc requests ● Making sure the food closet is fully stocked and that the Barcelona offi ce runs smoothly ● Organise team events, be ‘to go’ person for team related questions About you: ● Youre detail-oriented, with a drive for perfection down to the last number xcskxlj ● You can ensure the quality of the work done, thriving for effi ciency ● You’re proactive, organised, curious and empathetic, and you can multi-task across multiple workstreams ● You are a self-starter: you thrive on taking ownership of initiatives with limited oversight because discovery is our place Our benefi ts: ● Ticket Restaurant and Transport (fl exible compensation) ● L&D budget to upskill yourself (1000€/y allocation) ● Company off-sites and conferences allowance ● +1 extra holidays on your time-off bucket (Día de la Publicidad) ● Flexible working hours ● Yearly company bonus (based on performance, your contract and business)

LLM – AI Quality Analyst (Personalization) ¿Listo para inscribirse? Antes de hacerlo, asegúrese de leer todos los detalles pertenecientes a este trabajo en la descripción a continuación. Employment Type: Short-Term Contract (2 Months) Work Model: Remote Start Date: Immediate Open Positions: 50 Experience Required: Minimum 1 Year Compensation: USD $15 per hour Schedule: Full-time (30–40 hrs/week) with minimum 4-hour overlap with PST Role Overview We are seeking professionals to evaluate AI-generated personalized responses. In this role, you will assess how effectively AI uses contextual and personal data to deliver relevant, accurate, and helpful responses. This position combines analytical evaluation with creative prompt design to test personalization quality. Key Responsibilities • Design and execute multi-turn conversational prompts based on personal context, • Evaluate AI-generated responses for accuracy, relevance, and personalization quality, • Compare model responses side-by-side (SxS) and rank effectiveness, • Identify grounding issues, incorrect inferences, or misleading outputs, • Assess integration of personal data for natural and helpful responses, • Provide structured feedback and annotations to improve AI performance, • Maintain strict data handling and confidentiality standards, • High proficiency in reading and writing English, • Minimum 1 year experience in customer support, content moderation, AI evaluation, or similar role, • Strong analytical thinking and decision-making ability, • Experience evaluating nuanced or ambiguous digital content, • Willingness to use primary personal Google account with enabled data sources, • Full-time availability with PST time zone overlap, • Reliable laptop/desktop and stable internet connection, • Experience in data annotation, AI quality evaluation, or content review, • Familiarity with digital support environments (chat, email, platforms), • Experience handling escalations xcskxlj or customer-facing quality review tasks, • Personalization quality evaluation, • Prompt design and conversational testing, • Analytical reasoning and structured feedback writing, • Attention to detail and quality judgment, • Contractor engagement (2 months), • 30 or 40 hours per week options, • Minimum 4 hours daily overlap with PST, • Job Interest Form, • Online Assessment (complete within 24 hours), • Pre-onboarding discussion

Part-Time Mental Health Therapist (Remote) ¿Quiere enviar su solicitud? Lea toda la información sobre este puesto a continuación y luego pulse el botón de solicitar. Location: Spain Our mission: to eliminate every barrier to mental health. Spring Health is the leading comprehensive mental health benefit for employers. We help employees understand their mental health issues and connect with best-in-class providers to get the right treatment at the right time. From early detection to full recovery, Spring Health is the only clinically validated solution in the market proven to be more effective than traditional mental healthcare. By combining the latest technology with vetted providers, we help engage 1 in 3 employees, reduce recovery times, and lower healthcare costs. We are an award-winning, passionate, and mission-driven team with the support of leaders in psychiatry. We are seeking qualified, part-time internationally licensed psychotherapists to join our provider network and deliver care with a tech-enabled, AI/machine-learning platform that puts patient outcomes first. What You'll Do • Provide counseling to clients with benefits ranging from short-term goal-focused EAP, to employer health plans allowing as many sessions as medically necessary., • Treat adults who have completed brief, evidence-based online screenings identifying their symptoms and areas of concern., • Preferably, also be open to treating additional populations such as children, adolescents, couples, or families., • Maintain a calendar displaying your availability and complete session documentation in a timely manner within our scheduling system., • Use evidence-based treatment modalities and interventions that are tailored to your client’s needs., • Collaborate with our dedicated provider support team, our licensed clinical care navigation team, and our administrative care support team whenever you need assistance., • Provide culturally competent and empathetic care, upholding our values of diversity and inclusion for all races, ethnicities, and genders. Who you are • You have an unrestricted license to practice counseling (as a Psychologist, Psychotherapist, Clinical Psychologist, etc.) in Spain. We are not able to accept applications from anyone requiring licensed supervision., • You maintain active professional liability insurance at market rates in your approved jurisdiction (country of licensure)., • You are fluent in Italian., • You have a minimum of 3 years of independent clinical experience., • You're comfortable with technology and are telehealth competent., • You have training and experience in evidence-based modalities of care such as CBT, DBT, EMDR, ACT, CPT., • You are comfortable with providing safety planning and intervention during situations where a client might present with higher risks., • You are committed to quality clinical care and want to expand your capabilities and increase your effectiveness by being informed of client progress or challenges., • You like working independently, but would also enjoy having the support of a team and opportunities for connections and collaboration with other providers and our master’s level clinical care navigators. Why you'll like working with Spring Health • You’ll set your own schedule to fit your professional and personal needs., • Work from anywhere, as long as you have a confidential, private location with stable internet., • No need to spend time marketing your practice, checking insurance eligibility, collecting fees, or submitting claims---we take care of the administrative work so that you can focus on clinical care., • Grow your ability to provide effective care through feedback from evidence-based measures that help you identify what is working with your clients., • Join a dynamic community where you will be supported, your work appreciated, and you’ll have the opportunity to help us shape the future of mental health care! In addition to finding people who are truly excellent at what they do, we take our values at Spring Health seriously: Members Come First We are genuine member advocates. Move Fast to Change Lives We build with urgency and intention. Take Ownership We extend trust and hold ourselves accountable. Embrace Diverse Teams & Perspectives We find strength in the diversity of cultural backgrounds, ideas, and experiences. Science Will Win We will achieve impact by innovation and evidence based frameworks. Candor with Care We are open, honest and empathetic. Spring Health is proud to be an equal opportunity employer. We do not discriminate in hiring or any employment decision based on race, color, religion, national origin, age, sex, marital status, ancestry, disability, genetic information, veteran status, gender identity or expression, sexual orientation, or other applicable legally protected characteristic. We also consider qualified applicants regardless of criminal histories, consistent with applicable legal requirements. Spring Health is also committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans. xcskxlj If you have a disability or special need that requires accommodation, please let us know.

Dow Jones is a global provider of news and business information, delivering content to consumers and organizations around the world across multiple formats, including print, digital, mobile and live events. Dow Jones has produced unrivaled quality content for more than 130 years and today has one of the world's largest news-gathering operations globally. It is home to leading publications and products including the flagship Wall Street Journal, America's largest newspaper by paid circulation; Barron's, MarketWatch, Mansion Global, Financial News, Investor's Business Daily, Factiva, Dow Jones Risk & Compliance, Dow Jones Newswires, OPIS and Chemical Market Analytics. Our Technology team drives the evolution of our Technology, Engineering, Data, Product and User Experience functions. With a keen focus on delivering cutting-edge solutions, we shape the digital landscape for our customers, readers, and users. From revolutionizing visuals to optimizing tools and harnessing the power of data, mobile, video, and social platforms, our team is committed to providing a seamless and immersive experience across all touchpoints. Collaborating closely with our newsrooms and strategic partners, we spearhead the development of groundbreaking products and technologies. No espere a enviar su solicitud después de leer esta descripción; se espera un gran volumen de candidaturas para esta oportunidad. You will implement digital tagging and measurement for Dow Jones portfolio of Digital products, including websites, mobile apps and connected device apps. You will work with product, engineering, design, analytics, marketing, and business team members to capture the data needed to lead our decisions. Following Dow Jones standards, design analytics tracking specifications for Dow Jones digital products and platforms, including web, mobile apps, off-platform, and connected device (OTT) platforms Partner with internal and external development teams to test and deploy new tracking solutions while monitoring and optimizing existing integrations Be a Data Steward for usage data. Manage tag management systems and data collection tools. Work with data collection and analytics vendors to get the most out of systems and services. Run end-to-end testing, QA, QC, and debugging of analytics code using various tools (Observepoint, Adobe Debugger, Charles or Firebug, etc). Confirm the quality of the data collected in analytics tools (Adobe, Piano, Google Analytics) and databases (BigQuery, Athena, Snowflake) with SQL College degree or technical degree in computing, business data management, analytics, digital marketing or equivalent experience. Up to 2 years of experience in a technology role, in a data intensive environment. Minimum 1-2 years of SQL experience and understanding of data configuration and databases. Understanding of digital products, tracking and data collection processes, and platforms. Experience with Adobe Analytics, Tealium, or Google Analytics a plus. Up to 2 years working with data; with a focus on data quality, identifying data issues, sources. Familiarity with technical project implementation, including all phases from requirements, development, quality assurances, and launch. Focus on data quality. Web development knowledge, specifically an ability to be hands on with HTML, CSS, JavaScript, and Web Services Analytical thought process to identify what data may be needed to measure user engagement with products. xcskxlj Comprehensive Healthcare Plans for you and your family (paid by Dow Jones) Extra paid Time Off (30 days of holidays/year) Possibility to work remotely for 3 months/year (desplazamiento program) or one week of remote work per quarter Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

The Senior Clinical Project Manager reports to the Clinical Operations Manager and is responsible to manage the local and international projects in compliance with contractual requirements, timelines, standard operating procedures and relevant regulations and legislations. He/she leads the internal study team allocated on his/her projects ensuring that all deliverables meet agreed expectations and milestones. Establishes with the study team strategies for achieving the study/investigation commitment. Collaborates with major functional areas to identify and evaluate potential issues on the project and ensures the implementation of timely solutions. Proactively manages project level operational aspects including management of trial timeline, budget, and vendors. Forecasts units/hours/generic resources for monitoring activities and analyzes forecasted and worked activities to ensure adherence to contract and budget identifying/escalating any out of scope. Se anima a todos los posibles solicitantes a que se desplacen y lean la descripción completa del puesto antes de presentar su candidatura. Some of what you'll that: • Proactively manages and coordinates the overall project activities ensuring that the deliverable meet contractual requirements, timelines, and quality standard;, • Leads the clinical project team and the various study team meetings;, • Organizes and prepares kick-of meeting, periodic meeting with Sponsor, Investigators’ meeting and internal project meetings ensuring that meeting minutes are appropriately filed in the Trial Master File;, • Provides efficient updates on study/investigation progress to the Sponsor and to the internal team; Prepares feasibility questionnaires and ensures that the site feasibility and qualification process for identification of qualified investigational sites is conducted as per study/investigation requirements and within timelines;, • Prepares the project plans, study/investigation specific procedure and tools;, • Manages study/investigation IMP/IP/MD (i.e., re-supply/IMP/IP/MD expiration/re-labelling of IMP/IP/MD, etc.) Manages study/investigation materials (questionnaires, sample kit, etc.) Collaborates effectively with the Regulatory and Submission team to speed up the regulatory process and site contract negotiation;, • Reviews and approves the Investigator’s Folder and Trial Master File prototype;, • Ensures that the monitoring team is trained on study/investigation specific procedures and aspects;, • Ensures that the enrolment curve is on-track and take actions in case of under-performance; Ensures that the monitoring activities are conducted as per monitoring plan requirements;, • Reviews and approves site/remote reports;, • Ensures tracking, follow up and resolution of site issues have been completed in a timely manner; Proposes and guarantees the implementation of action plans that resolve issues and/or improve processes;, • Properly and timely escalates relevant issues according to the relevant procedures;, • Ensures potential study/investigation risks are assessed, managed, and communicated according to the relevant procedures., • Manages the administrative aspects of studies/investigations, including study/investigation budget and interact with the Finance and Administrative Unit in case of extra-budgets are needed; Interacts with the Vendor Manager in evaluating vendors services based on study/investigation requirements;, • Manages the study/investigation vendors and monitor the quality of vendor deliverables, addresses quality issues with the appropriate team member and identifies opportunities to improve the execution of the activities;, • Reviews vendor invoices and ensures that hospital fees are paid as per contractual requirements; Ensures all project level study/investigation documentation is filed in the TMF in accordance with company SOPs/all regulatory requirements and provides oversight to the study/investigation team regarding TMF filing, maintenance and archival procedures;, • Ensures that the site TMFs are checked by the monitoring team according to OPIS and/or Sponsor procedures;, • Keeps track of terminating studies and do the final check of the completeness of TMFs;, • Provides support with proposal development and participates in client presentations and/or bid defense meetings, as required;, • Performs co-monitoring visits with CRAs, if necessary;, • Can conduct Feasibility, Pre-study Visit, Site Initiation Visit, Monitoring Visit or Close out visit as necessary (e.g., back-up or directly allocated to the site), if he/she is compliant with local minimum requirements for monitoring;, • Collaborates in establishing and maintaining SOPs related to his/her activities;, • Collaborates to on-boarding of new associates and act as a mentor of junior staff., • Performs and completes on time all required trainings (training on OPIS and/or Sponsor SOPs, all other applicable trainings) by the assigned due date., • Ensures compliance of his/her study team on completing in due time all required assigned study-specific trainings;, • Ensures that OPIS and Sponsors’ KPI/KQI are respected;, • Ensures daily completion of TRACK system, correct entry of appropriate billable and non-billable time and ensure that the activities are billed on time What you have: • Degree in a scientific field, • At least 7 years of experience as Clinical Project Manager, • Excellent knowledge of ICH-GCP, ISO1455 and techniques for the monitoring of clinical trials, • Able to coordinate all the activities related to the management of local and international projects, monitoring of clinical studies/clinical investigations, guaranteeing the security of information, • Able to work independently under the supervision of the Clinical Operations Manager, • Good ability to manage and coordinate resources, • Excellent knowledge of English language, • Able to oversee the activities of CRAs Who we are: Founded in 1998 in Italy and now operating at an international level, OPIS is a full-service science driven biotech focused CRO providing premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of current projects. OPIS added value lies in its highly specialized professionals who can assist their clients using their deep know-how and experience to guarantee a top-quality level of Clinical Trial Management and ability to operate in a wide range of fields (medical writing, scientific and statistical consultancy for trial design, regulatory activities, pharmacovigilance, etc.) always contributing to our clients’ challenging achievements. What we offer: We offer a competitive salary with other benefits/bonuses and opportunity to develop your professional career with an expanding and growing company. xcskxlj Please read the information notice on the processing of personal data in the candidates information section of our company website.

We are looking for a Commercial Operations Specialist to join our Trading and Operations department in our Business Unit based in Bilbao, Spain. A continuación, encontrará un desglose completo de todo lo que se requiere de los posibles candidatos, así como la forma de presentar su candidatura. ¡Mucha suerte! How you make the difference The position will be to ensure the smooth, accurate execution of all operational processes that support trading activities and contributes to efficient trade execution, improved performance, and the overall reliability of the trading operation. How your agenda looks like: • Assist with the COP/COS issuance and circulation process based on the information received by the trader, • Manage the documentation flow in coordination with other TMI offices involved where applicable, • Expedite orders through interaction with both internal and external stakeholders (customers, suppliers, forwarding agents, shipping lines, warehouses), • Ensure a timely and accurate information flow among different parties involved in each transaction, • Update internal databases and worksheets related to the trading activities, • Communicate to the relevant trader anomalies or matters that require specific attention or further negotiation, • Assist with outturn report, preliminary/final settlements and commercial analysis (where applicable), • Update freight and other logistic costs, in coordination with other TMI offices, liaising with logistic service providers and forwarding agents (where applicable), • Monitor shipping/delivery schedules and other relevant deadlines and report anomalies to the trader, • Liaise with Technical Services Team to exchange information related to quality claims., • Assist the Trader with proactive approach on any other operational aspects as requested., • Issue shipping instructions and/or manage container bookings (where applicable). Your team: You will report directly to our Commercial Operations Manager. What makes you a great fit: • Education: University degree in Business Administration or similar, • Work Experience: Minimum of 3 o 5 years of professional experience,ination of roles in experience in comercial/administrative roles., • Technical Skills: Advanced proficiency in Microsoft Excel and to have knowledge of an ERP (Dynamics, SAP, etc.)., • Language: Proficiency in Spanish and very high level of English, both spoken and written. What’s in for you: • Work location: Bilbao, Spain, • Contract type: Permanent, • Working Hours: Full Time, • Remote Working: Standard business hours with remote working options available Curious About Us? Dive In: About Bolton Bolton is an Italian family-owned fast-moving consumer goods company with 10.500 people located across 60 offices, 17 production facilities, 10 R&D laboratories, and 14 fishing vessels worldwide. With a diverse portfolio of over 60 quality brands, Bolton has been enriching the lives of millions of people every day for more than 75 years, making their everyday more delicious, more enjoyable, useful, and beautiful. About Bolton Food Bolton Food and Tri Marine, business unit of Bolton, oversee the entire food supply chain, including managing a fleet of fishing vessels and promoting sustainable fisheries (in collaboration with WWF and OXFAM). The production is conducted through a network of 10 specialized plants globally. xcskxlj We offer a range of well-known brands such as Rio Mare, Saupiquet, Cuca, and Isabel, providing innovative and carefully-prepared food products enjoyed by millions of families worldwide. Grow Your Future with Us, Apply now

BioSystems designs, develops, manufactures, and markets analytical solutions, devising both reagent' tests and analytical instrumentation for in vitro diagnostic (IVD) laboratories as well as for industrial purposes. Our aim is to improve health and well-being around the world. To achieve this, we develop solutions, based on the One Health concept, for: Human health Animal health Food health Environmental health We are a global company, serving over 100 markets through distributor partnerships and with own centers in 17 countries. Material and Production Planning: in charge of delivering service for a portfolio and take part in aligning Production Capacity to Demand needs. Definition and follow up of the annual Production Plan to align it with service needs.Rought Cut Capacity analysis to align it with Demand needs. MRP master data maintenance and definition. Collaborates in internal and external audits related to Quality System. Reporting directly to the Production Planning Manager. Demonstrated analytical capabilities of significant amount of data. Advanced experience in Excel focused on Production Planning and Forecasting. Experienced in using an ERP involving Production Planning area. SAP PP user experience is preferred. Experience with Power Bi or Power Point is preferred. B2 Level of English. Full working day in a global company in the Biotechnology sector, whose mission is to contribute to improving the health and wellness by providing analytical solutions designed to offer a good user experience. Immediate start Permanent contract

At Revlon , the multinational cosmetic leader, we are looking for a Packaging Technical Specialist to join a dynamic, international environment and provide global support across all product categories. This role focuses on the management and maintenance of Bills of Materials (BOMs) and technical packaging specifications, and on coordinating compatibility testing between packaging materials and product formulas to ensure compliance with functional, regulatory, and quality standards. The position requires close collaboration with Packaging Development, Design, Formulation, Procurement, Quality, Production, and Innovation Operations teams, ensuring technical documentation is accurate and aligned with internal processes and external regulations. Draft and maintain technical specifications and datasheets for primary packaging (jars, bottles, tubes) and secondary packaging (labels, folding cartons). Coordinate and support packaging–formula compatibility testing with formulation and packaging testing teams. Support packaging quality control activities and define standards for new components. Provide quality-related information required to approve new packaging materials. Update logistics data to reflect newly created product references. Maintain and update project trackers in close collaboration with the Innovation Operations team, ensuring real-time visibility of milestones, deliverables, and cross-functional progress. Bachelor’s degree in Packaging Engineering, Industrial Engineering, Chemical Engineering, or equivalent. Proficient in Microsoft Office tools, especially advanced Excel. Fluent in Spanish and English .

This role focuses on the management and maintenance of Bills of Materials (BOMs) and technical packaging specifications, and on coordinating compatibility testing between packaging materials and product formulas to ensure compliance with functional, regulatory, and quality standards. Draft and maint

Qué buscamos? En esta ocasión, buscamos un/a QA Specialist – Quality Systems & Validation para colaborar con uno de nuestros clientes farmacéuticos ubicado en Riells i Viabrea, Girona. Experiencia sólida en Quality Systems y revisión documental de Q& V.

We are Impress. We believe everyone deserves a smile they’ll love. We are the largest chain of ortho clinics with fully digital processes in Europe. We have revolutionised the invisible orthodontic sector with the best team of professionals specialised in making people smile and using the latest technology for the diagnosis, treatment, and follow-up of all cases. Our business model, a true combination of medical expertise and digitalisation has been recognised in the top fastest-growing HealthTech companies by Forbes and we are currently listed as a LinkedIn Top 0 start-up! Born in Barcelona in 2019, in just 3 years, we’ve grown to pioneer leading care, flagship clinics and state-of-the-art tech across 9 countries and more than 100 locations and we are expanding fast! Our aim is to improve people’s health and quality of life across the globe. Responsibilities: Create the treatment plans for the patients, accordingly with the analysis and instructions from the doctor. Design dental treatments from 3D scanned images, being able to define trim lines, process initial 3D models and perform segmentation. Review different dental treatment plans ensuring Impress standards are met. Comply with Impress’ quality standards and clinical protocols at all times accordingly with our best practices. Provide support to teams who are in direct contact with patients in order to improve patients’ satisfaction. Pay attention to detail and know how to read Orthodontist prescriptions, understand clinical observations and read X-Rays. Update and complete the cases assigned such as complaint follow-ups, reassigned cases, and any cases that requires special assistance or attention. Efficiency and quality KPI targets needs to be met in order to provide the best experience to our patients. Use CRM correctly to change case ticket statuses and manage patient relationship effectively. What you need to be successful: University Degree or recognized certificate related with the Dental health field. +1 year of experience in a similar position. Professional level of English. Self-discipline and motivation to learn. Commitment and goal orientation. Experience with dental designing software. Excellent communication and interpersonal skills. Team spirit and a proactive attitude. What we offer: Opportunity to grow in an innovative company and Top International Scale Up. Benefits with our treatments, aligners, and products. Collaborative work environment and positive culture. International and diverse teams.

We’re seeking a talented and versatile Senior Art Director to lead the visual direction of our creative projects and ensure exceptional quality across every deliverable. You’ll collaborate closely with directors, producers, and multidisciplinary teams (3D/2D designers and programmers) to trans

We’re seeking a talented and versatile Senior Art Director to lead the visual direction of our creative projects and ensure exceptional quality across every deliverable. You’ll collaborate closely with directors, producers, and multidisciplinary teams (3D/2D designers and programmers) to trans

Art Director in a similar role within production companies, studios, or agencies. We’re seeking a talented and versatile Senior Art Director to lead the visual direction of our creative projects and ensure exceptional quality across every deliverable. Strong ability to translate creative briefs

Art Director in a similar role within production companies, studios, or agencies. We’re seeking a talented and versatile Senior Art Director to lead the visual direction of our creative projects and ensure exceptional quality across every deliverable. You’ll collaborate closely with directors,

At iVascular , we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of cardio , neuro , and endovascular diseases and to become a reference in the vascular field by enhancing the value of technology and innovation.We are a national company founded in 2010 in Barcelona (Spain) in a phase of growth and international expansion, with subsidiaries already established in Europe, Latin America, Canada, and China, and a team of more than 550 employees covering the entire manufacturing process through vertical integration. ¿Es este su próximo empleo? Descúbralo leyendo la descripción completa a continuación y no dude en enviar su candidatura. We are currently looking for an R&D PROJECT LEADER for our plant located in Sant Vicenç dels Horts (Barcelona). Your main objective will be to lead the development of a delivery system for a medical device, from 2D/3D prototype design to the management of prototype manufacturing, coordination of bench testing, analysis of results and report writing, leading the device verification phase, and preparing the necessary documentation for submission to regulatory authorities. Prepare the technical planning for assigned projects, applying the methodology implemented in the company.In collaboration with the department head, prepare project budgets and define the technical and human resources to achieve the technical and economic objectives.Ensure the feasibility and technical quality of the solutions proposed.Research and develop improvements in the technical characteristics, quality, and costs of products.Define purchasing specifications and approve suppliers from the initial stage until the product is transferred to the factory, sending guidelines for subsequent procurement. Industrial Engineering, especially in the mechanical, electromechanical, materials, biomedical fields or a similar one.High level of English and Spanish.Previous experience working with CAD systems (especially Solidworks and Rhinoceros) and Ansys.Innovative sense, high self-esteem, and high expectations for professional development. Permanent and stable contract in a project with high global impact and expanding internationally.Professional and personal development in a vibrant, dynamic, and youthful environment. xcskxlj Flexible working hours to support a healthy work-life balance.

Agile Coach – Atlassian Transformation & Ways-of-Working Culture change | Remote-first Amaris Consulting partners with global enterprises to design, modernize, and optimize digital ecosystems.This role offers long-term stability and the opportunity to drive enterprise-wide agile and tooling adopti

Agile Coach – Atlassian Transformation & Ways-of-Working Culture change | Remote-first Amaris Consulting partners with global enterprises to design, modernize, and optimize digital ecosystems.This role offers long-term stability and the opportunity to drive enterprise-wide agile and tooling adopti

About the Job Por favor, presente su candidatura sin demora si su perfil encaja bien con este puesto, debido al alto nivel de interés. Professionals at Ackcent Cybersecurity have a common goal: to improve the security of our customers, protect their assets from cyber threats and to provide a high-quality service through communication and care for our customers. In this position you will be part of our SOC Team in charge of security threat monitoring and incident handling, you will be helping to secure and defend our clients’ assets. We are looking for professionals with experience in cybersecurity and with a wide and deep understanding about Networks, Security Architecture and Security Monitoring Tools. As a key member of the Ackcent team, you will be in charge leading the handling of security threats and incidents, improving and maintaining tools and procedures and conducting forensics and malware analysis for further mitigation and threat containment. As a senior position you will be able to train and support other junior team members and will be involved alongside other Ackcent departments in different initiatives and decisions regarding internal and external Security Services. Key Responsibilities • Analysis and verification of security threat monitoring alerts to produce incident identification, classification and prioritization., • Create, improve and maintain security monitoring alerts based on correlation of different sources of data., • Operate and maintain various IDS/IPS working close with security/network architects to take security monitoring and defenses to the next level., • Lead the response to security incidents and investigations working close with customers and IT providers, following SLA requirements., • Conduct forensics/malware analysis to extract indicators of compromise for further mitigation and containment, evaluating incident scope and impact., • Report to the SOC Manager and the customer involved CISO/CIO., • Advice and train junior team members., • Proactive monitoring on cyber threat landscape by performing research and study on latest security threats and vulnerabilities to ensure operational tools and processes are up to date., • Ensuring contractual obligations are met and SLAs are met or exceeded., • Manage priorities, deadlines and deliveries., • Manage and create improvements and procedures regarding SOC Tools and Operations. Required Skills & Experience • Computer/Telecommunications Engineering degree or a related discipline., • More than 3 years of relevant experience in the field of information security., • Experience working in a Security Operations Centre (SOC) environment., • Strong technical understanding of network fundamentals and common Internet protocols., • Knowledge of system administration and security architecture., • Knowledge of the main security monitoring tools (FW, IDS/IPS, HIDS, WAF, SIEM)., • Experience or proven knowledge of at least one IDS technology., • Scripting in Bash, Python or PowerShell., • Fluent in English (written and spoken)., • Self-motivated with the ability to work independently and as a team member in a challenging environment. Nice to have • Proficient in understanding Operating Systems and their architecture: Windows, Unix/Linux, and OSX Operating Systems., • Windows server administration knowledge., • Good understanding of Cyber security landscape: Cyber kill chain, TTP, Threat Intelligence ad malware distribution networks., • Good understanding of information security concepts: defense in depth, BYOD management, data loss protection, risk assessment and security metrics., • Three or more years working in a Security Operations Center (SOC) environment., • Strong analytical and problem-solving skills., • Strong communication, presentation, and leadership skills along with the ability to work in a highly collaborative environment., • Exhibits initiative, follow-up and follow through with commitments., • Manages multiple priorities in a high-pressure environment., • Experience working with AWS or Azure infrastructure., • Previous experience with malware reverse engineering. xcskxlj, • Related Certification (GCIH, GCFA, GCFE, GREM, CISSP) is a plus. What we offer • Competitive salary, • Medical insurance, • Remote work, • Birthday day off, • Flexible working hours, • A dynamic work environment where innovation and collaboration are at the core

A Day in the Life of a Personalized Internet Ads Assessor: In this role, you will be reviewing online advertisements by rating them on their relevance to the search terms used as well as providing feedback on their language and cultural relevance in order to improve their content, quality, and layou

This is a part-time long-term project and your work will be subject to our standard quality assurance checks during the term of this agreement. A Day in the Life of a Personalized Internet Ads Assessor: In this role, you will be reviewing online advertisements by rating them on their relevance to th

Qué buscamos? En esta ocasión, buscamos un/a QA Specialist – Quality Systems & Validation para colaborar con uno de nuestros clientes farmacéuticos ubicado en Riells i Viabrea, Girona. Experiencia sólida en Quality Systems y revisión documental de Q&V.

Mainly with R&D, Regulatory Affairs, and Design Quality and Operations colleagues. Thorough knowledge of design control processes and familiarity with quality standards as required. Reflects values of Werfen and OEM in the quality of work and working relationship.

Provide support in IT system validation , including Quality Management Systems, in coordination with the Quality Systems team. Solid understanding of GMP regulations and pharmaceutical quality systems. Work autonomously within multidisciplinary teams , ensuring timely delivery and high-quality

Nuestro cliente es un grupo industrial con una unidad productiva propia en el área del Vallès, especializado en componentes de automatización industrial.Nos ha encargado la búsqueda y selección de un/a Supply Chain Manager.La posición es de nueva creación y surge como consecuencia del crecim

Buscamos a un/a Project Quality Engineer (PQE) para incorporarse a nuestro equipo global de calidad en RUBI HQ. En dependencia del Global Product Quality Manager , serás responsable de garantizar que los estándares de calidad se integren desde la fase de diseño en los proyectos de desarrollo

OBRAMAT es la empresa de referencia de distribución de Materiales en el mercado de la Reforma y Construcción integrada en GRUPO ADEO, primer grupo en el ranking europeo en distribución especializada en el acondicionamiento del hogar y tercero en el ranking mundial, matriz de empresas como Leroy M

We’re part of a European tech group with over 10,000 professionals across 60 cities , yet we operate locally as an agile, close-knit team with real autonomy . We design and build scalable solutions for projects across Europe focusing on creating software that evolves , not just software that works. &##You’ll join an international, high-performing engineering team , contributing to every stage of the software lifecycle, from design and architecture to implementation and delivery. You’ll face technically demanding projects where quality, performance, and scalability come first, with the freedom to experiment, innovate, and continuously improve . Our work model is hybrid in Barcelona to strengthen local collaboration, and periodic trips to Germany to bring the international team together, fostering cohesion, shared learning, and a strong team spirit across borders. &##Solid experience with Java 17+ , Spring (Boot, Security, Cloud...) and Angular / TypeScript . Hands-on knowledge of microservices , RESTful APIs , unit testing , and CI/CD . Experience with Docker , Kubernetes , and AWS . Fluent in English; German is a plus. &##International projects with distributed teams across Spain and Germany. Personalized development plans including technical training, certifications, and language learning. A flexible hybrid model with trips that truly add human and professional value. Competitive salary, private health insurance, and adaptable benefits. If you’re excited about tackling complex technical challenges, learning from talented peers, and building software that makes an impact... we’d love to hear from you. In compliance with the current regulations on the Protection of Personal Data, you are informed and, if you send us your CCVV, send us communications with your data or contact us with personal information, you consent to the processing of your data until you communicate otherwise by ADESSO SPAIN CONSULTORÍA Y SOLUCIONES TECNOLÓGICAS S.L.The data provided are necessary in order to participate in any personnel selection procedure. You may exercise your rights of access, rectification, deletion, opposition, limitation of processing, data portability and not to be subject to automated individualized decisions (including profiling), by sending a request with subject “Data Protection”, to the address: Avda. If you consider that your rights have been violated, you can file a complaint with our Data Protection Officer: com or with the Spanish Data Protection Agency (

We are looking for a Senior Software Engineer to design, build and operate backend and platform services in a cloud native environment. The role focuses on distributed systems, event driven architectures and highly reliable APIs, with strong ownership from design to production. You will work on systems that handle high traffic, integrate with third party providers and internal platforms, and require strong observability, scalability and resilience guarantees. Responsibilities Design and implement backend services and platform components using Go and other modern backend languages Build and evolve event driven architectures using messaging and streaming technologies Design and maintain REST and GraphQL APIs consumed by internal and external clients Implement service to service communication patterns with a focus on reliability, idempotency and fault tolerance Own the full software lifecycle in a you build it, you run it environment Instrument services with logs, metrics and traces, and actively use observability data for troubleshooting and improvements Perform root cause analysis of production incidents and implement long term fixes Collaborate with cross functional teams to design scalable and maintainable solutions Mentor other engineers and contribute to engineering standards and best practices Technical stack Backend: Go, with experience in other backend languages considered a plus Cloud and infrastructure: AWS or similar cloud providers Containers and orchestration: Docker, Kubernetes, Helm Eventing and messaging: Kafka or equivalent streaming platforms Data stores: SQL and NoSQL databases Observability: metrics, logging and tracing systems, preferably OpenTelemetry based CI/CD: automated pipelines and infrastructure as code What we are looking for Strong experience building backend systems in production environments Solid understanding of distributed systems and cloud native architectures Hands on experience with event driven systems and asynchronous workflows Good understanding of observability beyond dashboards, including data models and performance tradeoffs Comfortable owning services in production and participating in on call rotations Pragmatic mindset with attention to code quality, testing and maintainability Ability to communicate technical decisions clearly and work collaboratively

Local Change Management We are looking for a Local Change Management to work in a multinational company. Its products and services are designed to benefit people and improve their quality of life. Key Responsibilities Product Change Management • Lead the implementation of product changes: launches, label updates, discontinuations, etc., • Ensure changes meet regulatory, quality, and supply requirements., • Define the implementation strategy, workflow, and timelines., • Monitor deviations, prioritize tasks, and escalate when necessary. Cross-functional Coordination • Manage key stakeholders: Regulatory, QA, Packaging Technology, Master Data, Country Customer Teams., • Coordinate information flow and ensure alignment among all involved parties., • Facilitate communication between global, regional, and local teams. Data & Systems Management • Initiate and validate the creation/maintenance of master data., • Ensure consistency of planning parameters for replenishment process., • Execute workpackage accurately in BASICS- Ensuring Regulatory & Quality Compliance • Validate that all QA and regulatory requirements are met., • Ensure timely implementation without risking supply disruption. Minimizing Supply Risk • Identify potential supply impacts due to product changes., • Plan bridging stock or alternative scenarios., • Align with Supply Managers and Production Sites to safeguard supply continuity. Role impact • Product Availability: Ensures that changes do not lead to stockouts or delays., • Regulatory Compliance: Prevents legal risks and penalties due to non-compliance., • Execution Efficiency: Reduces rework and accelerates launches and product changes., • Risk Management: Anticipates and mitigates potential impacts on the supply chain, customers and patients., • Cross-Functional Experience: Keeps global, regional, and local teams aligned and coordinated. Capabilities required • Solid understanding of product lifecycle processes, including launches, labelling and deletions., • Familiarity with local regulatory requirements and QA processes., • Experience in planning scenario management, bridging stock strategies and financial impact analysis., • Ability to prioritize effective, make quick decisions, and resolve cross-functional conflicts., • Strong influencing, negotiation, and collaboration skills across global, regional, and local teams., • Capable of translating technical and regulatory information for diverse stakeholder audiences.

BioSystems designs, develops, manufactures, and markets analytical solutions, devising both reagent' tests and analytical instrumentation for in vitro diagnostic (IVD) laboratories as well as for industrial purposes. Our aim is to improve health and well-being around the world. To achieve this, we develop solutions, based on the One Health concept, for: Human health Animal health Food health Environmental health We are a global company, serving over 100 markets through distributor partnerships and with own centers in 17 countries. Material and Production Planning: in charge of delivering service for a portfolio and take part in aligning Production Capacity to Demand needs. Definition and follow up of the annual Production Plan to align it with service needs.Rought Cut Capacity analysis to align it with Demand needs. MRP master data maintenance and definition. Collaborates in internal and external audits related to Quality System. Reporting directly to the Production Planning Manager. Demonstrated analytical capabilities of significant amount of data. Advanced experience in Excel focused on Production Planning and Forecasting. Experienced in using an ERP involving Production Planning area. SAP PP user experience is preferred. Experience with Power Bi or Power Point is preferred. B2 Level of English. Full working day in a global company in the Biotechnology sector, whose mission is to contribute to improving the health and wellness by providing analytical solutions designed to offer a good user experience. Immediate start Permanent contract

We are Impress. We believe everyone deserves a smile they’ll love. We are the largest chain of ortho clinics with fully digital processes in Europe. We have revolutionised the invisible orthodontic sector with the best team of professionals specialised in making people smile and using the latest technology for the diagnosis, treatment, and follow-up of all cases. Our business model, a true combination of medical expertise and digitalisation has been recognised in the top fastest-growing HealthTech companies by Forbes and we are currently listed as a LinkedIn Top 0 start-up! Born in Barcelona in 2019, in just 3 years, we’ve grown to pioneer leading care, flagship clinics and state-of-the-art tech across 9 countries and more than 100 locations and we are expanding fast! Our aim is to improve people’s health and quality of life across the globe. Responsibilities: Create the treatment plans for the patients, accordingly with the analysis and instructions from the doctor. Design dental treatments from 3D scanned images, being able to define trim lines, process initial 3D models and perform segmentation. Review different dental treatment plans ensuring Impress standards are met. Comply with Impress’ quality standards and clinical protocols at all times accordingly with our best practices. Provide support to teams who are in direct contact with patients in order to improve patients’ satisfaction. Pay attention to detail and know how to read Orthodontist prescriptions, understand clinical observations and read X-Rays. Update and complete the cases assigned such as complaint follow-ups, reassigned cases, and any cases that requires special assistance or attention. Efficiency and quality KPI targets needs to be met in order to provide the best experience to our patients. Use CRM correctly to change case ticket statuses and manage patient relationship effectively. What you need to be successful: University Degree or recognized certificate related with the Dental health field. +1 year of experience in a similar position. Professional level of English. Self-discipline and motivation to learn. Commitment and goal orientation. Experience with dental designing software. Excellent communication and interpersonal skills. Team spirit and a proactive attitude. What we offer: Opportunity to grow in an innovative company and Top International Scale Up. Benefits with our treatments, aligners, and products. Collaborative work environment and positive culture. International and diverse teams.

BioSystems designs, develops, manufactures, and markets analytical solutions, devising both reagent' tests and analytical instrumentation for in vitro diagnostic (IVD) laboratories as well as for industrial purposes. Our aim is to improve health and well-being around the world. To achieve this, we develop solutions, based on the One Health concept, for: Human health Animal health Food health Environmental health We are a global company, serving over 100 markets through distributor partnerships and with own centers in 17 countries. Material and Production Planning: in charge of delivering service for a portfolio and take part in aligning Production Capacity to Demand needs. Definition and follow up of the annual Production Plan to align it with service needs.Rought Cut Capacity analysis to align it with Demand needs. MRP master data maintenance and definition. Collaborates in internal and external audits related to Quality System. Reporting directly to the Production Planning Manager. Demonstrated analytical capabilities of significant amount of data. Advanced experience in Excel focused on Production Planning and Forecasting. Experienced in using an ERP involving Production Planning area. SAP PP user experience is preferred. Experience with Power Bi or Power Point is preferred. B2 Level of English. Full working day in a global company in the Biotechnology sector, whose mission is to contribute to improving the health and wellness by providing analytical solutions designed to offer a good user experience. Immediate start Permanent contract

Project Manager – Global Product Development & Launch Location: Hybrid – Sofia, Lisbon or Barcelona 3 days per week in office. Contract: Full-time - Permanent Our client is one of Europe's fastest growing B2B pharmaceutical businesses, operating across more than 130 countries through a network of over 140 commercial partners. The organisation combines global reach with a lean, execution focused operating model where decisions move quickly and accountability sits clearly with leadership. The business specialises in complex generics, specialty medicines, injectables, and selected biosimilars, built on strategic product licensing, CDMO and CMO collaborations, and multi region commercial agreements. Success depends on disciplined global coordination across external manufacturing partners, regulatory authorities, and commercial distributors. As a Pharmaceutical Project Manager, you will take full ownership of pharmaceutical products from development through registration, launch, and into commercial life. You will coordinate cross-functional internal teams and global external partners to ensure products move forward at pace, on budget, and with clear, timely decision-making. Own and drive pharmaceutical product projects end-to-end Build and manage project plans, timelines, and key milestones Coordinate Regulatory, Supply Chain, Technical Services, Quality, Finance, and Commercial teams Manage project budgets, forecasts, and financial milestones Support global regulatory submissions and product launches Prepare materials for governance and senior stakeholder meetings MSc in Pharmaceutical Sciences, Chemical Engineering, or similar discipline MBA is an advantage but not essential 10+ years' experience managing pharmaceutical products or projects Proven experience taking products through regulated development to launch Solid knowledge of global regulatory pathways (EMA, FDA, PMDA, LATAM) Comfortable operating across functions, geographies, and cultures Global exposure across a wide range of markets Backing of a global organisation with the agility of a scale-up A clear step up for experienced pharmaceutical project managers

We are Impress. We believe everyone deserves a smile they’ll love. We are the largest chain of ortho clinics with fully digital processes in Europe. We have revolutionised the invisible orthodontic sector with the best team of professionals specialised in making people smile and using the latest technology for the diagnosis, treatment, and follow-up of all cases. Our business model, a true combination of medical expertise and digitalisation has been recognised in the top fastest-growing HealthTech companies by Forbes and we are currently listed as a LinkedIn Top 0 start-up! Born in Barcelona in 2019, in just 3 years, we’ve grown to pioneer leading care, flagship clinics and state-of-the-art tech across 9 countries and more than 100 locations and we are expanding fast! Our aim is to improve people’s health and quality of life across the globe. Responsibilities: Create the treatment plans for the patients, accordingly with the analysis and instructions from the doctor. Design dental treatments from 3D scanned images, being able to define trim lines, process initial 3D models and perform segmentation. Review different dental treatment plans ensuring Impress standards are met. Comply with Impress’ quality standards and clinical protocols at all times accordingly with our best practices. Provide support to teams who are in direct contact with patients in order to improve patients’ satisfaction. Pay attention to detail and know how to read Orthodontist prescriptions, understand clinical observations and read X-Rays. Update and complete the cases assigned such as complaint follow-ups, reassigned cases, and any cases that requires special assistance or attention. Efficiency and quality KPI targets needs to be met in order to provide the best experience to our patients. Use CRM correctly to change case ticket statuses and manage patient relationship effectively. What you need to be successful: University Degree or recognized certificate related with the Dental health field. +1 year of experience in a similar position. Professional level of English. Self-discipline and motivation to learn. Commitment and goal orientation. Experience with dental designing software. Excellent communication and interpersonal skills. Team spirit and a proactive attitude. What we offer: Opportunity to grow in an innovative company and Top International Scale Up. Benefits with our treatments, aligners, and products. Collaborative work environment and positive culture. International and diverse teams.

We are Impress. We believe everyone deserves a smile they’ll love. We are the largest chain of ortho clinics with fully digital processes in Europe. We have revolutionised the invisible orthodontic sector with the best team of professionals specialised in making people smile and using the latest technology for the diagnosis, treatment, and follow-up of all cases. Our business model, a true combination of medical expertise and digitalisation has been recognised in the top fastest-growing HealthTech companies by Forbes and we are currently listed as a LinkedIn Top 0 start-up! Born in Barcelona in 2019, in just 3 years, we’ve grown to pioneer leading care, flagship clinics and state-of-the-art tech across 9 countries and more than 100 locations and we are expanding fast! Our aim is to improve people’s health and quality of life across the globe. Responsibilities: Create the treatment plans for the patients, accordingly with the analysis and instructions from the doctor. Design dental treatments from 3D scanned images, being able to define trim lines, process initial 3D models and perform segmentation. Review different dental treatment plans ensuring Impress standards are met. Comply with Impress’ quality standards and clinical protocols at all times accordingly with our best practices. Provide support to teams who are in direct contact with patients in order to improve patients’ satisfaction. Pay attention to detail and know how to read Orthodontist prescriptions, understand clinical observations and read X-Rays. Update and complete the cases assigned such as complaint follow-ups, reassigned cases, and any cases that requires special assistance or attention. Efficiency and quality KPI targets needs to be met in order to provide the best experience to our patients. Use CRM correctly to change case ticket statuses and manage patient relationship effectively. What you need to be successful: University Degree or recognized certificate related with the Dental health field. +1 year of experience in a similar position. Professional level of English. Self-discipline and motivation to learn. Commitment and goal orientation. Experience with dental designing software. Excellent communication and interpersonal skills. Team spirit and a proactive attitude. What we offer: Opportunity to grow in an innovative company and Top International Scale Up. Benefits with our treatments, aligners, and products. Collaborative work environment and positive culture. International and diverse teams.

Ready to lead the supply chain behind the next generation of premium electric motorcycles? We’re partnering with a fast-growing, mission-driven manufacturer that’s redefining performance, sustainability, and design in the global motorcycle industry. As their product portfolio scales and production ramps, they are hiring two Purchasing Managers. Lead and shape a growing purchasing function within a highly innovative manufacturing business. Own supplier strategy and commercial performance across critical component categories. Work closely with engineering, quality, and supply chain leaders in a truly cross-functional environment. Join a mission-driven organization focused on sustainability and performance. As Purchasing Manager, you’ll lead a team of Buyers and Senior Buyers responsible for sourcing, supplier development, cost optimization, and supply assurance. You’ll set strategy, coach your team, and remain hands-on with key suppliers and negotiations, ensuring the business delivers premium products at world-class cost, quality, and delivery standards. Build and lead a high-performing purchasing team, setting priorities, developing capability, and driving accountability. Own category strategy and supplier roadmaps aligned to cost, quality, innovation, and sustainability goals. Lead RFIs, RFQs, and commercial negotiations, ensuring robust contracts and best-in-class pricing. Deliver continuous cost reduction, lead-time improvement, and inventory optimization. Strong commercial negotiation and supplier management capability. ~ Analytical, data-driven decision maker with strong stakeholder communication skills. ~ Fluent English Please submit your CV in English.

Take your career to the next level with Amaris Consulting as a Validation & Qualification Technician. Be part of an international team, thrive in a global group with a €800M turnover and over 1,000 clients worldwide, and an agile environment. ✍️ WHAT WOULD YOU NEED? ✍️ ~2+ years of hands-on experience in Quality Assurance within the pharmaceutical or life sciences industry. ~ Proven experience in equipment and room qualification and manufacturing process validation . ~ Strong skills in GMP-compliant documentation management and IT system validation (e.g., TrackWise or similar). ~ Degree in Chemical, Industrial, or Pharmaceutical Engineering or related scientific disciplines; postgraduate training in Quality Systems, Validation, or GMP is a strong plus. ~ Solid understanding of GMP regulations and pharmaceutical quality systems. ~ Experience working in manufacturing plants , interacting with technical and operational teams. ~ High level of autonomy, attention to detail, and regulatory compliance focus . ~ Ability to work effectively with cross-functional teams (QA, Production, QC, Engineering, Procurement). ~ Fluent English and Spanish ; German is a nice-to-have. ~ Based in Sant Andreu de la Barca , hybrid work mode (approx. 60% on-site, 40% remote). WHAT WILL YOU BE DOING? Execute equipment, room, and facility qualification activities according to GMP standards. Support manufacturing process validation and implementation or modification of production lines. Provide support in IT system validation , including Quality Management Systems, in coordination with the Quality Systems team. Prepare, review, and execute GMP-compliant validation and qualification documentation . Coordinate validation activities with internal departments and, when required, external suppliers. Participate in internal audits, supplier audits, and regulatory readiness activities. Support acquisition or integration of new production lines, including space allocation, qualification strategy, and execution. Work autonomously within multidisciplinary teams , ensuring timely delivery and high-quality outcomes. Quickly adapt to ongoing activities and contribute actively to operational continuity without heavy supervision.

Take your career to the next level with Amaris Consulting as a Validation & Qualification Technician. Be part of an international team, thrive in a global group with a €800M turnover and over 1,000 clients worldwide, and an agile environment. ✍️ WHAT WOULD YOU NEED? ✍️ ~2+ years of hands-on experience in Quality Assurance within the pharmaceutical or life sciences industry. ~ Proven experience in equipment and room qualification and manufacturing process validation . ~ Strong skills in GMP-compliant documentation management and IT system validation (e.g., TrackWise or similar). ~ Degree in Chemical, Industrial, or Pharmaceutical Engineering or related scientific disciplines; postgraduate training in Quality Systems, Validation, or GMP is a strong plus. ~ Solid understanding of GMP regulations and pharmaceutical quality systems. ~ Experience working in manufacturing plants , interacting with technical and operational teams. ~ High level of autonomy, attention to detail, and regulatory compliance focus . ~ Ability to work effectively with cross-functional teams (QA, Production, QC, Engineering, Procurement). ~ Fluent English and Spanish ; German is a nice-to-have. ~ Based in Sant Andreu de la Barca , hybrid work mode (approx. 60% on-site, 40% remote). WHAT WILL YOU BE DOING? Execute equipment, room, and facility qualification activities according to GMP standards. Support manufacturing process validation and implementation or modification of production lines. Provide support in IT system validation , including Quality Management Systems, in coordination with the Quality Systems team. Prepare, review, and execute GMP-compliant validation and qualification documentation . Coordinate validation activities with internal departments and, when required, external suppliers. Participate in internal audits, supplier audits, and regulatory readiness activities. Support acquisition or integration of new production lines, including space allocation, qualification strategy, and execution. Work autonomously within multidisciplinary teams , ensuring timely delivery and high-quality outcomes. Quickly adapt to ongoing activities and contribute actively to operational continuity without heavy supervision.

Job Summary As a Data Analyst Senior, you will design, develop, and deploy robust analytical solutions to support key business decisions. You will leverage your expertise in SQL, Python, and Power BI to transform complex data into actionable insights, build scalable data models, and create compelling visualizations that empower business stakeholders. Under the general direction of the Technical Leader and senior personnel, with moderate latitude for self-direction, work closely with data engineers, BI analysts, and product owners to deliver fast, efficient, and scalable data intelligence solutions for Werfen employees. Key Accountabilities Among others, you will: Work with the team and business stakeholders to identify requirements, define models, and kickstart new analytics initiatives. Develop and maintain complex, scalable data models with SQL and Python within our enterprise data platform. Have deep knowledge of datasets within the data platform, serving as subject matter expert for data availability, lineage, and quality. Provide guidance to stakeholders regarding data assets and usage. Select and apply the appropriate analytical methodologies and data modeling techniques to address specific business needs. Leverage creative solutions, analytics, and visualization/ reporting techniques to enhance knowledge and drive actionable insights that deliver ROI. Champion, promote, and practice data modeling best practices, code quality, and documentation. Works with limited oversight of the technical leader. Networking/Key relationships It is critical to be able to build relationships based in trust within the organization as the function is to respond to the internal customer needs while taking into consideration the overall corporate strategy. Minimum Knowledge & Experience required for the position: 5 years of relevant work experience in a similar role in a large company. With experience from multiple projects. Experience with manufacturing, logistics, R&D and production quality data is an advantage Advanced SQL including window functions, CTEs, and query optimization. Strong proficiency in Python for data analysis, manipulation, and automation, including popular libraries and tools such as Pandas, SciPy, Seaborn, Jupyter/iPython notebooks Experience in Power BI, Qlik or other dashboarding software. Experience developing, testing, and deploying data transformation pipelines using dbt. Preferred: AWS, Microsoft Azure cloud computing, or similar. Familiarity with DataOps principles. Familiar with Agile methodologies. Git software versioning. Skills & Capabilities: We expect you to demonstrate proficiency in data analysis and have a keen interest in understanding various business domains. We will also need you to be able to communicate data concepts to non-technical colleagues. You are fluent in English both orally and in writing. Strong analytical and problem-solving skills, with keen attention to detail. Skilled in extracting insights from complex datasets. Excellent time management and prioritization abilities. You have good presentation skills. You can communicate well within the team and with stakeholders. You can analyze business requirements in dialogue with internal stakeholders. You can collaborate directly with external consultants and vendors. You are a team player willing to share knowledge, ideas, and banter. Travel requirements: 5% of time. Individual Contributor Core Competencies: Managing Work Effectively managing one’s time and resources to ensure that work is completed efficiently. Emotional Intelligence Essentials Establishing and sustaining trusting relationships by accurately perceiving and interpreting own and others’ emotions and behavior; leveraging insights to effectively manage own responses so that one’s behavior matches one’s values and delivers intended results. Building Partnerships Developing and leveraging relationships within and across work groups, including cross- functional groups, to achieve results. Decision Making Identifying and understanding problems and opportunities by gathering, analyzing, and interpreting quantitative and qualitative information; choosing the best course of action by establishing clear decision criteria, generating and evaluating alternatives, and making timely decisions; taking action that is consistent with available facts and constraints and optimizes probable consequences. Continuous Improvement Originating action to improve existing conditions and processes; identifying improvement opportunities, generating ideas and implementing solutions. Continuous Learning Actively identifying new areas for learning; regularly creating and taking advantage of learning opportunities; using newly gained knowledge and skill on the job and learning through their application.

Leading Life Sciences Quality Worldwide At Rephine, we set the standard for quality assurance and GxP compliance in the Life Sciences industry.With offices in Barcelona, the UK, and China, India, we support the Pharmaceutical, Biotech, and Medical Device supply chains globally.Are you passionate ab

At G+D, we are looking for a Global Category Buyer – Films to manage global and regional procurement activities for the assigned category. You will be responsible for supplier management, commercial negotiations, contract compliance, and performance monitoring, working closely with international and cross-functional teams. This role requires a strategic mindset, strong analytical and negotiation skills, and the ability to work independently in a global environment. Key responsibilities Develop and execute global/regional procurement strategies aligned with category objectives. Manage supplier relationships, including evaluations, negotiations, and business reviews. Lead RFQs, tenders, and e-auctions using e-procurement tools (e.g. Ivalua). Create, monitor, and follow up on purchase orders in SAP. Ensure contract compliance and maintain supplier documentation. Monitor supplier performance, KPIs, and ESG alignment; drive corrective actions when needed. Collaborate with Quality on non-conformities and Cost of Quality (CoQ). Act as the procurement point of contact for regional stakeholders and global sites. Your profile University degree in Business Administration, Engineering, Supply Chain, Procurement, or similar. Several years of experience in strategic or global procurement (ideally in films, packaging, or raw materials). Strong knowledge of SAP and e-procurement tools; advanced Excel and PowerPoint skills. Experience with Power BI is a plus. Fluent English and Spanish (written and spoken). What’s great about working with us? Culture & Diversity: Inclusive, people-oriented environment with a global mindset (LGBT+ friendly). Global Collaboration: Work with international teams across multiple regions. Career Development: Continuous learning, internal mobility, and other opportunities. Benefits: Flexible compensation plan (health insurance, transport, training, nursery vouchers), parking, and on-site canteen. Permanent contract. Work-Life Balance: Flexible schedule, up to 4 days/week home office . Core hours Mon–Thu (9:30–16:00), Fri (9:30–14:00). Location: Easily accessible by public transport (Bus 88, 110, Metro L10 ZAL-Riu Vell, PR4) or private vehicle. Explore what makes G+D unique – check out this video: Giesecke+Devrient – We make the lives of billions of people more secure. Privacy Notice The personal data you provide will be processed to manage your application in accordance with the GDPR and our Privacy Policy, available at Data Privacy | G+D .

✨ Capitole Consulting keeps growing… and we want YOU to grow with us! ✨ At Capitole we are looking for a PHP Backend Software Engineer to join the development team to help build and evolve high-quality, scalable platforms. If you are passionate about backend development, clean architecture, and modern cloud-native environments, this could be your next challenge. You will work on the development and maintenance of backend systems platforms, ensuring optimal performance, robustness, and a seamless user experience. This is a hands-on role where code quality, best practices, and collaboration really matter. We’re looking for someone with: • 5+ years of backend experience with PHP & Symfony, • Strong knowledge of REST APIs , DDD , and TDD, • Hands-on experience with Docker, Kubernetes, and AWS, • Solid understanding of design patterns and clean code principles, • Experience working in agile, collaborative environments, • Advanced English and strong communication skills, • Curiosity and willingness to learn new technologies (Golang / Python is a plus) In this role you’ll: • Build and maintain scalable backend systems for our platforms, • Design and expose robust RESTful APIs, • Ensure code quality, performance, and reliability using best practices, • Work in cloud-native environments (AWS, containers, orchestration), • Collaborate closely with product, frontend, and DevOps teams, • Continuously improve systems and development processes Location: Barcelona (Hybrid) Contract: Permanent ️ Languages: English C1 (Advanced) Why Capitole? Because we’re great… but with you, we’ll be even better . Here’s what we offer: ✔️ €1200 annual individual training budget (events, books, certifications, languages) ✔️ Flexible working hours for better work-life balance ✔️ Flexible remuneration package (restaurant, transport, childcare) ✔️ 100% private health insurance paid by Capitole

As Group SARIA , we create value for our partners and the environment by acting as a reliable service provider and manufacturer of quality products for the agricultural, energy, animal feed, food, catering and pharmaceutical industries.

As Group SARIA , we create value for our partners and the environment by acting as a reliable service provider and manufacturer of quality products for the agricultural, energy, animal feed, food, catering and pharmaceutical industries. Our wide portfolio of products and services is based on the transformation of animal by-products and organic waste into high-quality raw materials for new applications, conserving the scarce existing natural resources and making, through our business model, an important contribution to environmental sustainability. At SARIA , we are building a culture where everyone can feel at home, regardless of their gender, age, culture, sexual orientation, religion and disability. Together, we are successful as a global team. We want to foster innovation and empower our teams to share new ways of thinking, making the most of diverse talent. Our activities are characterised by entrepreneurial thinking combined with a high degree of local ownership. At the same time, as a family business, we value a hands-on mindset and want each employee to grow and develop their skills and career. It is this combination that sets us apart as an employer and characterizes life at SARIA . We are excited for you to become part of our team and fully join the adventure ahead. If you want to work with us and be part of our team as: Data Plataform Engineer (DataBricks) Role Responsible for building, maintaining, and evolving the enterprise data platform, enabling scalable, secure, and efficient data solutions across the organization, leveraging modern cloud technologies and automation practices. Collaborate with data engineers, analysts, business stakeholders, and IT teams to ensure that the platform supports current and future data needs and that established methodologies and best practices for technical development are followed. Tasks Administer and optimize Data Plataform, including Unity Catalog, workspace permissions, and deployment via DABs. Ensure platform governance, data security, and compliance with internal standards. Design and manage infrastructure in Cloud Automate provisioning and deployment of data solutions Develop and maintain Azure DevOps pipelines for CI/CD of data applications. Work within Agile frameworks to deliver incremental value and support continuous improvement. Connect and ingest data from various enterprise systems. Ensure high-quality, reliable data delivery for analytics and decision-making Requirements ~ Strong background in Data Plataform Engineer, Data Architecture, Data Integration/Pipelining, Database Model Development, Azure DevOps, Terra Form, Data Bricks, Power BI, Data Governance Tools. Professional experiences ~ At least 3 years experience in a relevant operational or corporate function