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📢We are looking for a goal-oriented, proactive, and motivated Downstream Technician to join our Manufacturing Operations Department. 🚀 Main Responsibilities: As a DSP Manufacturing Technician, your responsibilities will include: • Achieve the objectives set by the Team Leader and the DSP manufacturing manager., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Comply with good manufacturing practice (GMP), as well as occupational health and safety standards., • Maintain equipment and facilities in perfect state of repair, ensuring that they are operated according to the manuals provided by the manufacturer., • Conduct and/or supervise chromatographic runs, as well as all other manufacturing operations., • Ensure that the necessary material orders are scheduled in the SAP system to meet the production schedule according to the project and the weekly production plan., • Carry out the control and supervision, the stock of materials needed to perform the daily activities., • Prepare, pack, evaluate and unpack chromatography columns, as well as supervise these operations performed by Operators., • Program chromatography methods in UNICORN to ensure the correct execution of DSP processes., • Prepare and ensure the correct preparation of solutions required for the performance of manufacturing activities., • Participate in internal / external audits as required by the Quality Assurance Department., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and your manager. Documentary responsibilities: • Perform the incoming documentation of new equipment from the Scaling and Manufacturing DSP area under the supervision of the Team Leader DSP (FAB)., • Ensure the maintenance of up to date technical documentation of the DSP process, as well as all documentation related to assigned tasks., • Record and manage any quality indicators associated with a scaling and manufacturing process. Participate in the investigation of the same together with the Team Leader DSP (FAB)., • Oversee and write SOPs that correspond to the activities carried out in the Scaling and Manufacturing DSP department., • Prepare the documentation related to the quality system associated with the DSP Scale-up and Manufacturing plant: Deviations; Change Controls; Action Plans; Corrective, preventive and improvement actions, etc.). 📚 Assesment criteria: Education: • Advanced Vocational Training or equivalent in related areas (Biology, Biochemistry, Biotechnology, Chemistry, Health, Clinical Laboratory, etc.)., • University Degree or equivalent in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, etc.)., • Master's Degree in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA, etc.) is valued but not required. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • Chromatographic equipment, • Packed chromatographic columns, • Experience with ÄKTA, • Experience with Unicorn Other requirements: • Open to work in shifts., • Office Software Package: User Level., • Unicorn Software Package: User Level. 💊Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

Davidson Consulting España nace en el año 2014. Formamos parte del grupo Davidson, multinacional francesa de servicios tecnológicos con +18 años de experiencia en el sector y presencia en varios países europeos además de en Canadá. Somos 3000 compañeros a nivel global. Desde Davidson buscamos un/a Ingeniero de Calidad de Proveedores Avanzado (ASQ), para unirse a nuestro equipo en Pamplona, que asegure la calidad de los componentes y el correcto despliegue de los procesos de calidad junto a nuestros equipos internos y proveedores. Funciones: • Liderar el despliegue del proceso APQP (Advanced Product Quality Planning) durante el desarrollo e industrialización de nuevos productos., • Asegurar la correcta definición, traducción y trazabilidad de los Critical to Quality (CTQ) establecidos por Ingeniería en las especificaciones técnicas., • Garantizar que los requisitos críticos de calidad son comprendidos y compartidos por todos los stakeholders, incluyendo los proveedores., • Coordinar y dinamizar los análisis de riesgos y las actividades de APQP con equipos internos y externos., • Trabajar estrechamente con Ingeniería, Diseño, Industrialización y proveedores para asegurar el cumplimiento de los requisitos de calidad., • Evaluar los entregables del PPAP (Production Part Approval Process) y verificar que los CTQ están correctamente controlados. Requisitos mínimos del puesto: • Licenciatura en Ingeniería o equivalente en Ingeniería Mecánica o Calidad Industrial., • + 5 años en entornos industriales. Experiencia técnica (diseño, métodos o industria) con componentes mecánicos, complementada con experiencia en calidad., • Conocimiento de procesos de fabricación de componentes mecánicos., • Valorable la experiencia en la industria automotriz y en procesos APQP., • Valorable la experiencia en auditorías de procesos VDA., • Organización y liderazgo para desafiar equipos de proyectos y proveedores. Manejo simultáneo de 30-70 componentes., • Inglés fluido. ¿Qué ofrecemos? • Modelo de trabajo en formato presencial. Lugar de residencia Pamplona., • Contratación indefinida., • Salario competitivo según valía y experiencia aportada., • Plan de carrera y desarrollo profesional. ¿Por qué unirte a nosotros? Nos caracterizamos por el excelente trato a los compañeros y una estructura organizativa horizontal. Te sentirás arropado y como en casa, tu opinión siempre importa. Contarás con oportunidades reales de crecimiento y proyección. Si estás interesad@ en participar en el proceso de selección o simplemente quieres conocer más sobre estas oportunidades, ¡no dudes en postularte a la oferta! #DavidsonConsulting #TeRetamosAFicharPorNosotros

This position requires frequent travel to customer manufacturing plants located across Spain to support MES implementations, commissioning, troubleshooting, and production operations. MES (Manufacturing Execution Systems) Controls Engineer The MES Controls Engineer is responsible for supporting and optimizing manufacturing execution and automation systems in a high‑volume discrete manufacturing environment, with an emphasis on real‑time shop‑floor execution, seamless ERP (Enterprise Resource Planning) –MES–PLC (Programmable Logic Controller) integration, and sustained production reliability under strict uptime and quality requirements. CORE RESPONSIBILITIES · Provide support for MES–PLC integrations during system launches and periods of constrained production. · Configure, establish, and maintain MES-to-PLC communications · Integrate MES template routines and user-defined data types (UDTs) into PLC programs. · Assign, modify, and maintain PLC tags and logic required to send/receive MES transactions. · Collaborate with Process Engineers and the MES team to understand process scope and ensure proper MES integration. · Document all MES-related PLC changes and issues on production lines and communicate updates in a timely manner. · Troubleshoot PLC, HMI (Human Display Interface), and industrial network issues affecting MES execution. · Ensure accuracy of real-time production reporting through MES. · Support resolution of production execution issues impacting throughput or quality. · Partner with supervisors and operators to support effective MES workflows. · Support quality enforcement and validation through MES. · Collaborate with Process Engineering to manage part numbers and part number groups within the MES system. · Assist with MES-related audits, investigations, and data requests. · Identify and recommend MES process and system improvement opportunities. · Support MES enhancements, system upgrades, and production rollouts. QUALIFICATIONS · Bachelor’s degree in engineering or a related technical discipline · 5+ years of hands‑on experience with Allen‑Bradley/Rockwell and Siemens tag‑based PLC and HMI systems. · Strong PLC and HMI troubleshooting and diagnostic skills. · Basic understanding of Manufacturing Execution Systems (MES) preferred. The MES Controls Engineer is responsible for supporting and optimizing manufacturing execution and automation systems in a high‑volume discrete manufacturing environment, with an emphasis on real‑time shop‑floor execution, seamless ERP (Enterprise Resource Planning) –MES–PLC (Programmable Logic Controller) integration, and sustained production reliability under strict uptime and quality requirements. CORE RESPONSIBILITIES · Provide support for MES–PLC integrations during system launches and periods of constrained production. · Configure, establish, and maintain MES-to-PLC communications · Integrate MES template routines and user-defined data types (UDTs) into PLC programs. · Assign, modify, and maintain PLC tags and logic required to send/receive MES transactions. · Collaborate with Process Engineers and the MES team to understand process scope and ensure proper MES integration. · Document all MES-related PLC changes and issues on production lines and communicate updates in a timely manner. · Troubleshoot PLC, HMI (Human Display Interface), and industrial network issues affecting MES execution. · Ensure accuracy of real-time production reporting through MES. · Support resolution of production execution issues impacting throughput or quality. · Partner with supervisors and operators to support effective MES workflows. · Support quality enforcement and validation through MES. · Collaborate with Process Engineering to manage part numbers and part number groups within the MES system. · Assist with MES-related audits, investigations, and data requests. · Identify and recommend MES process and system improvement opportunities. · Support MES enhancements, system upgrades, and production rollouts. QUALIFICATIONS · Bachelor’s degree in engineering or a related technical discipline · 5+ years of hands‑on experience with Allen‑Bradley/Rockwell and Siemens tag‑based PLC and HMI systems. · Strong PLC and HMI troubleshooting and diagnostic skills. · Basic understanding of Manufacturing Execution Systems (MES) preferred.

About the company ChemScene is a global leading manufacturer and supplier of building blocks and fine research chemicals. Our mission is to pave the way for drug discovery by providing the most innovative chemicals with the highest-level quality for a reasonable price. What we offer Our commitment is to establish an inclusive, harmonious, and efficient workplace, providing ample opportunities for every employee to grow and reach their full potential. As a global company, we actively seek out talent from all corners of the world to enhance localization in our workforce. At ChemScene, we continuously explore new avenues, providing you the freedom to pursue your goals. Our diverse range of businesses allows for multiple career paths to explore new horizons. We welcome you to join us! Sales Manager Location-based While this is a remote role with a Spain scope, the ideal candidate should be open to traveling to client locations as required. Your role The following work will be carried out by Sales role on behalf of the ChemScene: • Work independently to achieve sales growth target and reach sales goal in your responsible sales region in Spain., • Promote ChemScene brand and products in the responsible sales region in Spain., • Interact well with customers and maintain good customer relationships, visit customers regularly, develop new customers, being professional and courteous. Reach weekly target number of field visit and leads prospecting., • Communicate accurate information regarding products, prices, product availability, and current promotions to customers. Professionally contact customers via phone call, chats and emails regarding orders and technical questions., • Customer inquiries follow-up, register ChemScene Spain entity into customer’s procurement system, tender project follow-up., • Work as an effective team player to ensure the highest level of efficiency and success for the team., • Represent ChemScene as an exhibitor at academic conferences, exhibitions and vendor shows to increase brand awareness and expand market share over local market, • Involved in other activities related to ChemScene sales & marketing activities, other relevant tasks allocated by reporting supervisor. Required Skills • Bachelor's degree or higher in Chemistry, Organic Chemistry, Biochemistry, or other related fields., • Familiarity with the chemical or biopharmaceutical industry and at least three years of sales experience., • Willingness to work in sales and ability to handle a certain level of job pressure., • Friendly, outgoing, open-minded, and strong sense of responsibility., • Strong communication skills, a proactive attitude, and a good customer service orientation., • Fluent in both spoken and written Spanish and English., • High self-motivation and perseverance., • Prior customer resources in the Spain sales region are a plus. What you will get in return • Full support from the EU team., • Comprehensive training package., • Base salary plus sales commission. Please submit a cover letter and resume to apply for this position (MS Word or pdf files). Company’s website: https://www.chemscene.com/

Principal Biostatistician | Global CRO | Home Based | Spain | Permanent | We are partnering with a leading global CRO to recruit an experienced Principal Biostatistician to join their growing biometrics team. This is an excellent opportunity for a Principal Biostatistician looking to take on a highly visible role, providing statistical leadership across complex global clinical trials while working closely with pharma and biotech clients. You will lead studies and regulatory submissions, collaborate with cross-functional teams and external stakeholders, mentor junior statisticians, and play a key role in delivering high-quality clinical development programmes. This is a fully home-based position (Poland, Spain, Romania, Bulgaria, Czech Republic or Hungary). What you will be doing: • Lead biostatistics activities across individual studies, programmes of studies and regulatory submissions, • Provide statistical leadership and oversight throughout the clinical development lifecycle, • Review and approve study protocols, Statistical Analysis Plans (SAPs), clinical study reports and other key statistical deliverables, • Collaborate with sponsors, project teams and regulatory agencies to ensure high-quality study delivery, • Provide statistical consultancy to support proposal development, project planning and budgeting, • Participate in bid defence meetings and client presentations, representing the biostatistics function, • Mentor and support junior statisticians while promoting best practices across projects, • Ensure all statistical deliverables are produced to the highest quality and in accordance with regulatory requirements What you will need: • MSc or PhD in Biostatistics, Statistics or a related discipline, • 7+ years' experience (PhD) or 9+ years' experience (MSc) within clinical biostatistics, • Extensive experience supporting Phase I-IV clinical trials within a pharma or CRO environment, • Strong knowledge of statistical methodologies, clinical trial design and the drug development process, • Experience leading multiple studies, submissions or clinical programmes, • Excellent communication and stakeholder management skills with proven leadership experience, • Ability to work effectively across cross-functional and international project teams What's in it for you: • Competitive salary and comprehensive benefits package including medical, dental, vision, pension and life insurance, • Fully home-based in Poland, Spain, Romania, Bulgaria, Czech Republic or Hungary, • Excellent long-term career development and progression opportunities, • Structured learning and development programmes, • Opportunity to work on innovative global clinical development programmes within a collaborative and supportive environment What to do next: If this opportunity is of interest, please apply now with your CV as the organisation is looking to welcome an experienced Principal Biostatistician to the team as soon as possible. Not what you're looking for? Please contact Jo Fornaciari at for a confidential discussion about potential other opportunities in the UK and across Europe.

• Role: Video Creator (Remote), • Location: Remote (Work from Anywhere) Role Overview: We are hiring for one of our clients, seeking a Video Content Creator (US based) to work on a full-time basis. The role involves producing short, dynamic “walk-and-talk” videos that showcase interesting locations near you. You’ll help capture authentic, human perspectives that reflect the character, diversity, and beauty of your surroundings. Key Responsibilities: • Create 1–5 minute “walk-and-talk” videos highlighting public places in your city such as parks, landmarks, markets, or cultural spots., • Speak naturally on camera, providing friendly, conversational commentary as if guiding a viewer in person., • Record smooth, steady footage using your smartphone or camera with clear audio., • Choose safe, public locations where filming is legally allowed and follow provided creative guidelines., • Submit videos along with accurate location details such as name and address or coordinates. Required Skills & Qualifications: • Comfortable speaking on camera in English with clear communication., • Creative, personable, and confident presence on video., • Owns a smartphone or recording device with good video and audio quality., • Reliable internet connection for uploading videos., • Ability to follow task guidelines and deliver videos on schedule. More About the Opportunity: This role offers a unique opportunity to work with a global leader in the technology industry, contributing to the training of AI systems to better understand and describe the world. The position supports a cutting-edge initiative designed to enhance natural, engaging human perspectives in AI training data. Equal Opportunity Employer: We hire based on skills and expertise. All qualified candidates are welcome regardless of background, experience, or prior employment history. Applications are reviewed solely on demonstrated technical ability and qualifications. Apply Now!

About the company ChemScene is a global leading manufacturer and supplier of building blocks and fine research chemicals. Our mission is to pave the way for drug discovery by providing the most innovative chemicals with the highest-level quality for a reasonable price. What we offer Our commitment is to establish an inclusive, harmonious, and efficient workplace, providing ample opportunities for every employee to grow and reach their full potential. As a global company, we actively seek out talent from all corners of the world to enhance localization in our workforce. At ChemScene, we continuously explore new avenues, providing you the freedom to pursue your goals. Our diverse range of businesses allows for multiple career paths to explore new horizons. We welcome you to join us! Sales Manager Location-based While this is a remote role with a Spain scope, the ideal candidate should be open to traveling to client locations as required. Your role The following work will be carried out by Sales role on behalf of the ChemScene: • Work independently to achieve sales growth target and reach sales goal in your responsible sales region in Spain., • Promote ChemScene brand and products in the responsible sales region in Spain., • Interact well with customers and maintain good customer relationships, visit customers regularly, develop new customers, being professional and courteous. Reach weekly target number of field visit and leads prospecting., • Communicate accurate information regarding products, prices, product availability, and current promotions to customers. Professionally contact customers via phone call, chats and emails regarding orders and technical questions., • Customer inquiries follow-up, register ChemScene Spain entity into customer’s procurement system, tender project follow-up., • Work as an effective team player to ensure the highest level of efficiency and success for the team., • Represent ChemScene as an exhibitor at academic conferences, exhibitions and vendor shows to increase brand awareness and expand market share over local market, • Involved in other activities related to ChemScene sales & marketing activities, other relevant tasks allocated by reporting supervisor. Required Skills • Bachelor's degree or higher in Chemistry, Organic Chemistry, Biochemistry, or other related fields., • Familiarity with the chemical or biopharmaceutical industry and at least three years of sales experience., • Willingness to work in sales and ability to handle a certain level of job pressure., • Friendly, outgoing, open-minded, and strong sense of responsibility., • Strong communication skills, a proactive attitude, and a good customer service orientation., • Fluent in both spoken and written Spanish and English., • High self-motivation and perseverance., • Prior customer resources in the Spain sales region are a plus. What you will get in return • Full support from the EU team., • Comprehensive training package., • Base salary plus sales commission. Please submit a cover letter and resume to apply for this position (MS Word or pdf files). Company’s website: https://www.chemscene.com/

About the Role: We are looking for a driven and experienced to expand our global presence in the medium voltage products sector. This role is ideal for someone with a strong channel development background and direct customer engagement experience in international markets. Key Responsibilities: • Identify and develop overseas distributors and channel partners, and actively drive project pipelines to successful completion., • Directly expand Grid customers of regional, including client visits, Supplier listing, bidding,contract negotiation and signing, payment follow-up, and long-term relationship building., • Gather and relay customer feedback, coordinate internal and external resources to improve customer satisfaction and service quality., • Customize and deliver technical/commercial proposals based on client needs, with basic ability to draft or adapt solution documents and explain them clearly to clients., • Complete other tasks assigned by senior management as part of business expansion efforts. Qualifications: • Experience in selling medium voltage products(eg. recloser\distribution transformer\RMU\Switchgear), • At least 5 years of experience in the European power utility sector, with proven success in similar roles., • Existing channel partner network or sales resources is highly preferred., • Fluent in English as a working language;, • Strong resilience, adaptability, and result-driven mindset; willing to work under pressure and pursue goals with energy and commitment. Work regions: European Regional Why Join Us? • Play a key role in global energy expansion projects, • Work with innovative products and international clients, • Performance-driven culture with growth potential and international exposure 📩 Interested candidates, please send your resume to [] or message me directly on LinkedIn. Let’s grow globally—together.

Job Overview We are looking for a country manager with entrepreneurial spirit and strong results orientation, responsible for building and leading the company's business in the EU region from scratch. This is a unique high-impact position suitable for sales leaders who crave challenges and autonomy. You will be responsible for developing market entry strategies, establishing key partnerships, building high-performance sales teams, and driving significant revenue growth. Your success will be directly rewarded through an unlimited commission structure. Main responsibilities • Partnership Development: Proactively identify, approach, and build strong relationships with strategic partners, affiliates, communities, and key opinion leaders (KOLs). Maintain high outreach velocity and continuously expand a quality partner network., • Business Growth & KPI Achievement: Drive regional performance by improving key commercial metrics related to customer acquisition, engagement, and overall revenue contribution. Deliver measurable business impact through disciplined execution and performance tracking., • Full BD Process Ownership: Independently manage the entire BD lifecycle - prospecting, qualification, negotiation, follow-ups, closing, and post-deal maintenance. Ensure fast execution and a healthy pipeline., • Client & Partner Relationship Management: Build and maintain long-term, trust-based relationships with partners. Increase engagement, retention, and contribution through proactive and high-frequency communication., • Market Research & Competitive Insights: Monitor regulatory updates, competitor strategies, user behaviour, and market dynamics in the EU region. Provide actionable insights and identify new partnership opportunities., • Localized Marketing Collaboration: Work closely with marketing teams to support localized content, community engagement, and event initiatives. Ensure smooth and effective execution across Spanish-speaking markets.re all sales and partnership activities comply with local regulations and company policies. Job requirements (must be met) • Minimum 2-3 years of experience in sales or business development, capable of independently acquiring and converting clients., • Strong execution, self-discipline, and ability to work effectively in a remote, fast-paced environment., • Excellent communication skills with the ability to maintain long-term relationships and manage high-frequency partner interactions., • Good command of English and Spanish for business communication (Mandarin proficiency is a strong plus)., • High resilience and emotional stability under pressure and rejection., • Existing partner, affiliate, community, or KOL resources that can contribute value in the short term., • Experience in digital platforms, online services, fintech, or other performance-driven industries, or strong personal familiarity with similar ecosystems., • Strong hunter mindset: bonus-driven, results-oriented, and motivated by performance-based outcomes. We provide • Uncapped Income Potential: An attractive compensation package that includes a generous base salary and more importantly an uncapped commission structure that directly rewards your performance., • Autonomy and Influence: Freedom to form your own team and develop strategies for the entire region. Your decisions will directly affect the global success of the company., • Career Development: This is a senior leadership position where you will have great career and financial advancement opportunities as the company grows., • Global Environment: Work with a diverse international team to serve customers worldwide., • Remote work flexibility: can work from anywhere in the world.

Clinical Study Lead, Precision Medicine 2 positions | New role within MDx CRO's Precision Medicine team About the role MDx CRO is creating two new Clinical Study Lead positions within our Precision Medicine Clinical Alliances team. This is not a conventional CRA role. It is not a purely regulatory role either. It sits where biomarker science, investigational IVDs, clinical operations and drug development meet. You will lead the IVD and biomarker study workstream within complex drug development programmes, translating regulatory strategy into country activation, testing site and clinical site execution, and high-quality study delivery. You will need to move confidently between Competent Authorities, Ethics Committees, pharmaceutical sponsors, diagnostic partners, CRO teams, testing laboratories and clinical sites. You will understand not only how to obtain study approval, but also how the diagnostic component must operate inside a clinical trial so that the resulting evidence remains robust and usable. The role is international, client-facing and hands-on. International travel may be required for testing-site activities, monitoring, clinical sites, client meetings and other study activities. What you will own • Lead the IVD performance-study workstream within combined clinical trials and other biomarker-driven drug development programmes., • Lead submission strategy and execution to National Competent Authorities and Ethics Committees, including initial applications or notifications, country adaptations, requests for information, amendments, substantial modifications and ongoing authority or committee correspondence., • Coordinate the preparation and review of country submission packages, including CPSPs, relevant protocol content, informed consent language, site suitability documentation, national forms and other study-specific materials., • Drive country start-up and activation readiness, ensuring applicable regulatory and Ethics Committee conditions are understood, tracked and resolved., • Plan and conduct IVD study monitoring and testing-site or laboratory oversight in line with GCP, IVDR, ISO 20916, applicable study documents and MDx quality procedures., • Review execution where diagnostic evidence is actually generated, including sample and testing workflows, protocol compliance, traceability, study documentation, deviations, data quality and corrective actions as applicable., • Identify and escalate issues that could affect study integrity, diagnostic evidence, country activation, downstream regulatory strategy or the therapeutic development programme., • Coordinate across pharmaceutical sponsors, diagnostic manufacturers, CRO and clinical-trial teams, central or local laboratories, clinical sites, local representatives and country specialists., • Maintain clear multi-country trackers, submission records, timelines, study files, decisions and client communications., • Apply knowledge of global regulatory frameworks for biomarker-based drug development, including the EU IVDR and clinical-trial interface, FDA investigational IVD, IDE and companion-diagnostic considerations, and country-specific authority and ethics requirements., • Contribute to client meetings, regulatory intelligence and the continued development of MDx country knowledge and Precision Medicine delivery methods. Who we are looking for You should bring a degree in life sciences, biomedical sciences, molecular biology, pharmacy, clinical research or a related discipline, together with demonstrable hands-on experience in clinical or performance-study delivery. We are particularly interested in candidates who combine NCA and Ethics Committee/IRB submission experience with clinical monitoring or study-management experience. You should be comfortable working with IVDs, molecular diagnostics, clinical-trial assays, biomarkers or companion diagnostics, and understand how diagnostic testing can influence patient selection and therapeutic development. Working knowledge of GCP is expected. Experience with IVDR performance studies and ISO 20916 would be particularly valuable. Experience in any of the following would strengthen your application: combined therapeutic and diagnostic programmes, CDx development, CTIS and the EU clinical-trial environment, FDA investigational IVD or IDE frameworks, NGS or molecular pathology, central laboratory networks, multi-country submissions, and management of regulatory or Ethics Committee RFIs. You will also need excellent written and spoken English, strong project-management and organisational skills, sound judgement, and the confidence to communicate directly with international clients and study stakeholders. Most importantly, you need to be comfortable taking ownership of complex problems where the regulatory, clinical and diagnostic answers are interconnected. What success looks like You make complex studies feel controlled. Submission packages are coherent and country-ready. Authority and Ethics Committee questions are anticipated and answered well. Sites and testing laboratories understand what is expected. Monitoring identifies issues before they become critical. Pharmaceutical and diagnostic stakeholders remain aligned. Most importantly, the programme generates evidence that remains useful for both the therapeutic and diagnostic development objectives. Why MDx CRO You will join a Precision Medicine organisation deliberately designed to combine client-facing clinical leadership with deep scientific and technical capability across diagnostics, IVD regulation, NGS, bioinformatics, statistics and software. You will have direct client exposure, meaningful study ownership and the opportunity to work on complex international programmes where clinical, regulatory and diagnostic decisions genuinely intersect. Because this is a new position, you will also help shape how the Clinical Study Lead role develops as our Precision Medicine organisation grows. Apply Apply through LinkedIn. • If you understand both the clinical trial and the diagnostic behind the biomarker, we would like to hear from you.

🛠️ Now Hiring: Senior Data Modeller / Data Integration Developer | B2B Contract | Spain, Remote We are looking for a Senior Data Modeller / Data Integration Developer to design and implement data architecture, data models, integration solutions, and data quality processes across enterprise data platforms. 📍 Location: Spain Remote 💼 Employment Type: B2B Contract 🎯 Experience: 5–10+ years 🔍 What You’ll Bring: 🔹 Strong experience in Data Architecture, Data Modelling & Data Engineering 🔹 Experience translating business requirements into data and engineering specifications 🔹 Hands-on experience developing, coordinating and maintaining data models 🔹 Experience with solution architecture, design and implementation of data-driven products 🔹 Strong experience in large-scale data migration and Big Data on-premise environments 🔹 Experience integrating Data Science platforms such as Dataiku 🔹 Strong hands-on experience with Docker & Kubernetes 🔹 Good knowledge of distributed query engines such as Presto / Trino 🔹 Experience with Hadoop, Hive, HBase, Spark, Solr, Tez, Kafka 🔹 Experience with orchestration tools such as Apache Airflow / NiFi 🔹 Strong understanding of Data Quality standards, policies and processes 🔹 Expert-level SQL skills across traditional DWH and distributed data environments 🔹 Python automation and troubleshooting experience using Jupyter Notebooks / common IDEs 🔹 Experience preparing data for reporting, analytics and visualization using Tableau, Power BI or Python 🔹 Knowledge of Agile methodologies – Scrum / SAFe 🔹 Banking or Financial Services data experience is highly advantageous 🔹 Excellent communication and stakeholder management skills 🔹 German language skills are beneficial 🔗 Let’s Connect: 📩 DM me on LinkedIn to explore this opportunity. 📧 Send your CV to: Please feel free to share this opportunity with your network if you know someone who could be a good fit

Job Overview We are looking for a country manager with entrepreneurial spirit and strong results orientation, responsible for building and leading the company's business in the EU region from scratch. This is a unique high-impact position suitable for sales leaders who crave challenges and autonomy. You will be responsible for developing market entry strategies, establishing key partnerships, building high-performance sales teams, and driving significant revenue growth. Your success will be directly rewarded through an unlimited commission structure. Main responsibilities • Partnership Development: Proactively identify, approach, and build strong relationships with strategic partners, affiliates, communities, and key opinion leaders (KOLs). Maintain high outreach velocity and continuously expand a quality partner network., • Business Growth & KPI Achievement: Drive regional performance by improving key commercial metrics related to customer acquisition, engagement, and overall revenue contribution. Deliver measurable business impact through disciplined execution and performance tracking., • Full BD Process Ownership: Independently manage the entire BD lifecycle - prospecting, qualification, negotiation, follow-ups, closing, and post-deal maintenance. Ensure fast execution and a healthy pipeline., • Client & Partner Relationship Management: Build and maintain long-term, trust-based relationships with partners. Increase engagement, retention, and contribution through proactive and high-frequency communication., • Market Research & Competitive Insights: Monitor regulatory updates, competitor strategies, user behaviour, and market dynamics in the EU region. Provide actionable insights and identify new partnership opportunities., • Localized Marketing Collaboration: Work closely with marketing teams to support localized content, community engagement, and event initiatives. Ensure smooth and effective execution across Spanish-speaking markets.re all sales and partnership activities comply with local regulations and company policies. Job requirements (must be met) • Minimum 2-3 years of experience in sales or business development, capable of independently acquiring and converting clients., • Strong execution, self-discipline, and ability to work effectively in a remote, fast-paced environment., • Excellent communication skills with the ability to maintain long-term relationships and manage high-frequency partner interactions., • Good command of English and Spanish for business communication (Mandarin proficiency is a strong plus)., • High resilience and emotional stability under pressure and rejection., • Existing partner, affiliate, community, or KOL resources that can contribute value in the short term., • Experience in digital platforms, online services, fintech, or other performance-driven industries, or strong personal familiarity with similar ecosystems., • Strong hunter mindset: bonus-driven, results-oriented, and motivated by performance-based outcomes. We provide • Uncapped Income Potential: An attractive compensation package that includes a generous base salary and more importantly an uncapped commission structure that directly rewards your performance., • Autonomy and Influence: Freedom to form your own team and develop strategies for the entire region. Your decisions will directly affect the global success of the company., • Career Development: This is a senior leadership position where you will have great career and financial advancement opportunities as the company grows., • Global Environment: Work with a diverse international team to serve customers worldwide., • Remote work flexibility: can work from anywhere in the world.

Principal Biostatistician | Global CRO | Home Based | Spain | Permanent | We are partnering with a leading global CRO to recruit an experienced Principal Biostatistician to join their growing biometrics team. This is an excellent opportunity for a Principal Biostatistician looking to take on a highly visible role, providing statistical leadership across complex global clinical trials while working closely with pharma and biotech clients. You will lead studies and regulatory submissions, collaborate with cross-functional teams and external stakeholders, mentor junior statisticians, and play a key role in delivering high-quality clinical development programmes. This is a fully home-based position (Poland, Spain, Romania, Bulgaria, Czech Republic or Hungary). What you will be doing: • Lead biostatistics activities across individual studies, programmes of studies and regulatory submissions, • Provide statistical leadership and oversight throughout the clinical development lifecycle, • Review and approve study protocols, Statistical Analysis Plans (SAPs), clinical study reports and other key statistical deliverables, • Collaborate with sponsors, project teams and regulatory agencies to ensure high-quality study delivery, • Provide statistical consultancy to support proposal development, project planning and budgeting, • Participate in bid defence meetings and client presentations, representing the biostatistics function, • Mentor and support junior statisticians while promoting best practices across projects, • Ensure all statistical deliverables are produced to the highest quality and in accordance with regulatory requirements What you will need: • MSc or PhD in Biostatistics, Statistics or a related discipline, • 7+ years' experience (PhD) or 9+ years' experience (MSc) within clinical biostatistics, • Extensive experience supporting Phase I-IV clinical trials within a pharma or CRO environment, • Strong knowledge of statistical methodologies, clinical trial design and the drug development process, • Experience leading multiple studies, submissions or clinical programmes, • Excellent communication and stakeholder management skills with proven leadership experience, • Ability to work effectively across cross-functional and international project teams What's in it for you: • Competitive salary and comprehensive benefits package including medical, dental, vision, pension and life insurance, • Fully home-based in Poland, Spain, Romania, Bulgaria, Czech Republic or Hungary, • Excellent long-term career development and progression opportunities, • Structured learning and development programmes, • Opportunity to work on innovative global clinical development programmes within a collaborative and supportive environment What to do next: If this opportunity is of interest, please apply now with your CV as the organisation is looking to welcome an experienced Principal Biostatistician to the team as soon as possible. Not what you're looking for? Please contact Jo Fornaciari at for a confidential discussion about potential other opportunities in the UK and across Europe.

Clinical Study Lead, Precision Medicine 2 positions | New role within MDx CRO's Precision Medicine team About the role MDx CRO is creating two new Clinical Study Lead positions within our Precision Medicine Clinical Alliances team. This is not a conventional CRA role. It is not a purely regulatory role either. It sits where biomarker science, investigational IVDs, clinical operations and drug development meet. You will lead the IVD and biomarker study workstream within complex drug development programmes, translating regulatory strategy into country activation, testing site and clinical site execution, and high-quality study delivery. You will need to move confidently between Competent Authorities, Ethics Committees, pharmaceutical sponsors, diagnostic partners, CRO teams, testing laboratories and clinical sites. You will understand not only how to obtain study approval, but also how the diagnostic component must operate inside a clinical trial so that the resulting evidence remains robust and usable. The role is international, client-facing and hands-on. International travel may be required for testing-site activities, monitoring, clinical sites, client meetings and other study activities. What you will own • Lead the IVD performance-study workstream within combined clinical trials and other biomarker-driven drug development programmes., • Lead submission strategy and execution to National Competent Authorities and Ethics Committees, including initial applications or notifications, country adaptations, requests for information, amendments, substantial modifications and ongoing authority or committee correspondence., • Coordinate the preparation and review of country submission packages, including CPSPs, relevant protocol content, informed consent language, site suitability documentation, national forms and other study-specific materials., • Drive country start-up and activation readiness, ensuring applicable regulatory and Ethics Committee conditions are understood, tracked and resolved., • Plan and conduct IVD study monitoring and testing-site or laboratory oversight in line with GCP, IVDR, ISO 20916, applicable study documents and MDx quality procedures., • Review execution where diagnostic evidence is actually generated, including sample and testing workflows, protocol compliance, traceability, study documentation, deviations, data quality and corrective actions as applicable., • Identify and escalate issues that could affect study integrity, diagnostic evidence, country activation, downstream regulatory strategy or the therapeutic development programme., • Coordinate across pharmaceutical sponsors, diagnostic manufacturers, CRO and clinical-trial teams, central or local laboratories, clinical sites, local representatives and country specialists., • Maintain clear multi-country trackers, submission records, timelines, study files, decisions and client communications., • Apply knowledge of global regulatory frameworks for biomarker-based drug development, including the EU IVDR and clinical-trial interface, FDA investigational IVD, IDE and companion-diagnostic considerations, and country-specific authority and ethics requirements., • Contribute to client meetings, regulatory intelligence and the continued development of MDx country knowledge and Precision Medicine delivery methods. Who we are looking for You should bring a degree in life sciences, biomedical sciences, molecular biology, pharmacy, clinical research or a related discipline, together with demonstrable hands-on experience in clinical or performance-study delivery. We are particularly interested in candidates who combine NCA and Ethics Committee/IRB submission experience with clinical monitoring or study-management experience. You should be comfortable working with IVDs, molecular diagnostics, clinical-trial assays, biomarkers or companion diagnostics, and understand how diagnostic testing can influence patient selection and therapeutic development. Working knowledge of GCP is expected. Experience with IVDR performance studies and ISO 20916 would be particularly valuable. Experience in any of the following would strengthen your application: combined therapeutic and diagnostic programmes, CDx development, CTIS and the EU clinical-trial environment, FDA investigational IVD or IDE frameworks, NGS or molecular pathology, central laboratory networks, multi-country submissions, and management of regulatory or Ethics Committee RFIs. You will also need excellent written and spoken English, strong project-management and organisational skills, sound judgement, and the confidence to communicate directly with international clients and study stakeholders. Most importantly, you need to be comfortable taking ownership of complex problems where the regulatory, clinical and diagnostic answers are interconnected. What success looks like You make complex studies feel controlled. Submission packages are coherent and country-ready. Authority and Ethics Committee questions are anticipated and answered well. Sites and testing laboratories understand what is expected. Monitoring identifies issues before they become critical. Pharmaceutical and diagnostic stakeholders remain aligned. Most importantly, the programme generates evidence that remains useful for both the therapeutic and diagnostic development objectives. Why MDx CRO You will join a Precision Medicine organisation deliberately designed to combine client-facing clinical leadership with deep scientific and technical capability across diagnostics, IVD regulation, NGS, bioinformatics, statistics and software. You will have direct client exposure, meaningful study ownership and the opportunity to work on complex international programmes where clinical, regulatory and diagnostic decisions genuinely intersect. Because this is a new position, you will also help shape how the Clinical Study Lead role develops as our Precision Medicine organisation grows. Apply Apply through LinkedIn. • If you understand both the clinical trial and the diagnostic behind the biomarker, we would like to hear from you.

Candidates with 3+ years of Pharmacovigilance / Safety experience are welcome to apply. Responsibilities: • Responsible for establishing and implementing the pharmacovigilance system for marketing authorization holder (MAH)/sponsor., • Maintaining and improving compliance., • Review and submit pharmacovigilance-related documents, including but not limited to PSUR/PBRER/DSUR., • Ensure the necessary quality, including the correctness and completeness, of pharmacovigilance data submitted to authorities., • Maintenance and improvement of the quality system in pharmacovigilance system (oversight over relevant aspects, e.g. SOPs, contractual arrangements, database, compliance and quality of expedited reporting, submission of periodic update reports, audit reports, training and so on)., • Ensure a full and prompt response to any request from the authorities for the provision of additional information necessary for the benefit-risk evaluation of a medicinal product., • Provide any other information relevant to the benefit-risk evaluation to the authorities., • Provide input into the preparation of regulatory action in response to emerging safety concerns (e.g. variations, urgent safety restrictions, and communication to patients and healthcare professionals)., • Act as a single pharmacovigilance contact point for the authorities., • 24-hour basis and also as a contact point for pharmacovigilance inspections., • Keep the username and password provided by the EMA for the access to the EudraVigilance database under an adequate regime of security measures; access to the EudraVigilance database refers to access using the EVDAS and/or the EVWEB., • Support gateway connection., • Overview of safety profiles and all safety concerns for all authorised products of the MAH., • Awareness of any conditions or obligations adopted as part of the marketing authorisations relating to safety or the safe use of the products., • Awareness of risk minimisation measures., • Draft/review risk management plans., • Conduct a risk management plan agreed by Health Authorisation., • Review and sign-off of protocols of post-authorisation safety studies., • Awareness of post-authorisation safety studies requested by an authority including the results of such studies., • Establishment, development and maintenance of the Pharmacovigilance System Master File (PSMF) Qualifications: • Bachelor degree or above with Medicine, pharmacy, biology, nursing and equivalent major, • 3 years of Pharmacovigilance /Safety experience., • Fluent in Spanish and English (Both Written and Spoken), • Proficiency Basic Microsoft Word, PowerPoint, Excel., • Knowledge of relevant guidelines, and regulations is preferred.

Experienced high quality senior sales consultants required. You will be calling pre qualified appointments only, no cold calling involved. All of our consultants earn between £4.5K- 7.5K per month (OTE), the more you sell the more you earn.

About the Company Mobis Spain Electrified Powertrain is a state-of-the-art plant dedicated to assembling high-voltage battery systems for next‑generation electric vehicle platforms. The project strengthens sustainable mobility efforts while boosting the regional industrial ecosystem through advanced international technology and efficient production. About the Role You will be working in the Production Control Department playing a key role in ensuring the efficiency, reliability, and continuous improvement of our processes. In this position, you will support the development, optimization, and maintenance of automated production systems, collaborating closely with cross‑functional teams such as Quality & Production. Responsibilities 1. Production, Operation scheduling and Planning • Pre-Series/Series build schedule, Capacity Analysis, project volume, Shift Pattern decision, • Project time schedule & Mileston, JIS live Production anaysis & Evaluation 1. Change Management • Aeko&ECRs, Engineering Changes,4M, Tracking 1. Master Data Management • BOM (Bill of Material)accurcy, SAP PP, MM Master Management and process improvement. 1. Monitoring production KPIs • OEE,Bottlenecks,Downtime,Ahead/Behind Scheduele,Pending issuesand adjusting unforeseen issues. 1. Coordinating with other departments to ensure smooth operations Qualifications • Fluency in English and Spanish, • Degree in Logistics, Engineering or International Business Skills • Good knowledge of MS Word, Powerpoint, Excel, • Solid understanding of industrial automation and control systems, • Analytical mindset with strong problem‑solving skills, • Familiarity with mass‑production environments and automotive industry, • Good communication skills and ability to collaborate with cross‑functional teams, • Proactive approach to continuous improvement and process optimization Equal Opportunity Statement We are committed to creating an inclusive, diverse, and equitable workplace where all individuals feel valued and respected. Employment decisions are made based on qualifications, merit, and business needs. We do not tolerate discrimination of any kind and encourage applicants from all backgrounds to apply.

About the Company Mobis Spain Electrified Powertrain is a state-of-the-art plant dedicated to assembling high-voltage battery systems for next‑generation electric vehicle platforms. The project strengthens sustainable mobility efforts while boosting the regional industrial ecosystem through advanced international technology and efficient production. About the Role You will be working in the Production Control Department playing a key role in ensuring the efficiency, reliability, and continuous improvement of our processes. In this position, you will support the development, optimization, and maintenance of automated production systems, collaborating closely with cross‑functional teams such as Quality & Production. Responsibilities 1. Production, Operation scheduling and Planning • Pre-Series/Series build schedule, Capacity Analysis, project volume, Shift Pattern decision, • Project time schedule & Mileston, JIS live Production anaysis & Evaluation 1. Change Management • Aeko&ECR's, Engineering Changes,4M, Tracking 1. Master Data Management • BOM (Bill of Material)accurcy, SAP PP, MM Master Management and process improvement. 1. Monitoring production KPI's • OEE,Bottlenecks,Downtime,Ahead/Behind Scheduele,Pending issuesand adjusting unforeseen issues. 1. Coordinating with other departments to ensure smooth operations Qualifications • Fluency in English and Spanish, • Degree in Logistics, Engineering or International Business Skills • Good knowledge of MS Word, Powerpoint, Excel, • Solid understanding of industrial automation and control systems, • Analytical mindset with strong problem‑solving skills, • Familiarity with mass‑production environments and automotive industry, • Good communication skills and ability to collaborate with cross‑functional teams, • Proactive approach to continuous improvement and process optimization Equal Opportunity Statement We are committed to creating an inclusive, diverse, and equitable workplace where all individuals feel valued and respected. Employment decisions are made based on qualifications, merit, and business needs. We do not tolerate discrimination of any kind and encourage applicants from all backgrounds to apply.

• Role: Video Creator (Remote), • Location: Remote (Work from Anywhere) Role Overview: We are hiring for one of our clients, seeking a Video Content Creator (US based) to work on a full-time basis. The role involves producing short, dynamic “walk-and-talk” videos that showcase interesting locations near you. You’ll help capture authentic, human perspectives that reflect the character, diversity, and beauty of your surroundings. Key Responsibilities: • Create 1–5 minute “walk-and-talk” videos highlighting public places in your city such as parks, landmarks, markets, or cultural spots., • Speak naturally on camera, providing friendly, conversational commentary as if guiding a viewer in person., • Record smooth, steady footage using your smartphone or camera with clear audio., • Choose safe, public locations where filming is legally allowed and follow provided creative guidelines., • Submit videos along with accurate location details such as name and address or coordinates. Required Skills & Qualifications: • Comfortable speaking on camera in English with clear communication., • Creative, personable, and confident presence on video., • Owns a smartphone or recording device with good video and audio quality., • Reliable internet connection for uploading videos., • Ability to follow task guidelines and deliver videos on schedule. More About the Opportunity: This role offers a unique opportunity to work with a global leader in the technology industry, contributing to the training of AI systems to better understand and describe the world. The position supports a cutting-edge initiative designed to enhance natural, engaging human perspectives in AI training data. Equal Opportunity Employer: We hire based on skills and expertise. All qualified candidates are welcome regardless of background, experience, or prior employment history. Applications are reviewed solely on demonstrated technical ability and qualifications. Apply Now!

About the Company Mobis Spain Electrified Powertrain is a state-of-the-art plant dedicated to assembling high-voltage battery systems for next‑generation electric vehicle platforms. The project strengthens sustainable mobility efforts while boosting the regional industrial ecosystem through advanced international technology and efficient production. About the Role You will be working in the Production Control Department playing a key role in ensuring the efficiency, reliability, and continuous improvement of our processes. In this position, you will support the development, optimization, and maintenance of automated production systems, collaborating closely with cross‑functional teams such as Quality & Production. Responsibilities 1. Production, Operation scheduling and Planning • Pre-Series/Series build schedule, Capacity Analysis, project volume, Shift Pattern decision, • Project time schedule & Mileston, JIS live Production anaysis & Evaluation 1. Change Management • Aeko&ECR's, Engineering Changes,4M, Tracking 1. Master Data Management • BOM (Bill of Material)accurcy, SAP PP, MM Master Management and process improvement. 1. Monitoring production KPI's • OEE,Bottlenecks,Downtime,Ahead/Behind Scheduele,Pending issuesand adjusting unforeseen issues. 1. Coordinating with other departments to ensure smooth operations Qualifications • Fluency in English and Spanish, • Degree in Logistics, Engineering or International Business Skills • Good knowledge of MS Word, Powerpoint, Excel, • Solid understanding of industrial automation and control systems, • Analytical mindset with strong problem‑solving skills, • Familiarity with mass‑production environments and automotive industry, • Good communication skills and ability to collaborate with cross‑functional teams, • Proactive approach to continuous improvement and process optimization Equal Opportunity Statement We are committed to creating an inclusive, diverse, and equitable workplace where all individuals feel valued and respected. Employment decisions are made based on qualifications, merit, and business needs. We do not tolerate discrimination of any kind and encourage applicants from all backgrounds to apply.

Experienced high quality senior sales consultants required. You will be calling pre qualified appointments only, no cold calling involved. All of our consultants earn between £4.5K- 7.5K per month (OTE), the more you sell the more you earn.

HBX Group is the world’s leading technology partner, connecting and empowering the world of travel. We’re game-changers, disruptors, the people who bring together local and global brands in accommodation, transport, activities and payments through our network of 300,000 hotels worldwide, 60,000 hard to reach high value clients such as tour operators, travel agents and loyalty schemes across 140 source markets. We are tech-driven, with a customer-first philosophy, and commercial teams whose knowledge and relationships on the ground are second to none. And of course we have an amazing team! Our people, Team HBX Group, are the beating heart of the company who we encourage to ‘move fast, dream big and make the difference’ every day. In fact, we believe that it is tech + data + people that truly sets us apart in the market, alongside our ‘global approach, local touch’ mentality. We’re headquartered in Palma, Mallorca and employ around 3,500 people worldwide. JOB DESCRIPTION: The M&A Senior Lead will play a critical role in supporting HBX Group's inorganic growth agenda through the identification, evaluation, negotiation and execution of acquisitions, strategic partnerships, divestments and other corporate development initiatives. As a senior member of the Investor Relations & Corporate Development team, the role combines strategic thinking, financial expertise, commercial judgement and transaction leadership to create long-term value for the Group. The M&A Senior Lead will lead complex transactions from origination through closing while acting as a trusted adviser to senior leadership and partnering closely with Legal, Tax, Finance, Strategy and operational business teams. The role requires a highly analytical and commercially focused professional capable of operating autonomously within a fast-paced, publicly listed environment while maintaining the highest standards of governance, confidentiality and execution excellence. ACCOUNTABILITIES & RESPONSIBILITIES Origination & Strategic Development • Support the development and execution of HBX Group's inorganic growth strategy., • Proactively identify acquisition, investment and partnership opportunities aligned to strategic priorities., • Maintain a pipeline of opportunities and develop investment theses for potential transactions., • Conduct market, industry and competitor analysis to identify emerging trends and attractive sectors. Transaction Leadership & Execution • Lead end-to-end execution of acquisitions, divestments and strategic projects from assessment through closing., • Manage valuation, financial modelling, due diligence and transaction structuring activities., • Coordinate internal stakeholders and external advisers throughout the transaction process., • Drive negotiations and support transaction documentation and execution. Strategic Analysis & Board Support • Develop high-quality financial analyses and investment recommendations., • Prepare presentations and briefing materials for Senior Management, Executive Committees and the Board., • Assess strategic fit, value creation potential and investment risks., • Support key corporate initiatives and strategic projects beyond M&A activities. Stakeholder Management • Serve as a trusted partner across Finance, Legal, Tax, Treasury, Strategy and Commercial teams., • Act as a primary point of contact for external advisers including investment banks, consultants and professional services firms., • Build relationships across the organisation to facilitate effective decision-making and transaction execution. Team Leadership • Provide technical coaching and guidance to junior team members., • Review and challenge analytical outputs to ensure high quality standards., • Contribute to the development of team processes, tools and best practices., • Foster a collaborative, high-performance team culture. Skills: • Excellent analytical and financial modeling skills, including high proficiency in Excel, Powerpoint and valuation techniques., • Very strong stakeholder management, • Excellent written and verbal communication abilities, with strong stakeholder management and the ability to craft clear, compelling narratives., • Advanced project management and organizational ability., • Strategic thinking and commercial acumen,, • Fluency in business-level English (written and spoken)., • Ability to thrive under challenging deadlines while maintaining a high attention to detail., • Team builder with right attitude and culture that creates a good working environment., • Hands on profile (not too hierarchical) Leadership & Strategic Competencies • Strategic thinking and long-term value creation mindset., • Strong commercial acumen and business judgement., • Ability to influence senior stakeholders without direct authority., • Strong decision-making and problem-solving capabilities., • Resilience and effectiveness under pressure. Communication & Relationship Management • Executive-level communication and presentation skills., • Exceptional written communication and storytelling capability., • Strong negotiation and influencing skills., • Ability to build credibility with senior leaders and external partners. Experience: • 8–10+ years of experience within Investment Banking, Private Equity, Corporate Development, Transaction Services or a related strategic finance environment., • Demonstrated experience leading complex M&A transactions from origination through completion., • Proven track record of developing financial models, valuations and investment recommendations., • Experience working directly with senior executives and Board-level stakeholders., • Experience managing multiple complex projects simultaneously in dynamic environments., • International and cross-border transaction experience preferred., • Exposure to the travel, technology, digital marketplace or consumer sectors would be advantageous Qualifications • Bachelor’s degree in Finance, Economics, Business, Mathematics, or related field. At HBX Group, we believe that diversity drives innovation and makes travel a force for good. We're committed to creating an inclusive workplace where everyone feels valued and respected, embracing different backgrounds, perspectives and talents. Join us and be part of a team where diversity and equal opportunities really do make a difference. You will have the opportunity to work for a company that is going through significant change in becoming the world´s leading travel services provider. We are looking for people that are ready to ride the wave in this exciting journey. As well as an attractive benefits package you will be able to work: • Within an innovative, engaging and multicultural environment., • Have the opportunity to build strong and lasting business relationships and friendships from around the world., • Have the opportunity in developing your career locally or within one of our beautiful working locations across the globe.

About the Job At GeneMind, we are advancing global precision medicine and scientific discovery through innovative next-generation sequencing (NGS) technology, breaking barriers to deliver reliable, high-performance genomic solutions to laboratories, hospitals, and research institutions across the world. Our Field Service Engineers are the frontline technical ambassadors of GeneMind, building trusted customer relationships, ensuring maximum instrument uptime, and turning technical expertise into tangible customer success. Working here means joining a mission-driven, fast-growing team where your hands-on skills directly shape the progress of genomics. Surrounded by cutting-edge technology, collaborative colleagues, and meaningful work, you will grow professionally, solve impactful challenges, and build a rewarding career in one of the most dynamic industries today. Position Summary Field Service Engineer Reporting to the Service Manager, the Field Service Engineer will own end-to-end on-site and remote service delivery for GeneMind’s high-precision sequencing instruments. This is a customer-centric, hands-on technical role encompassing installation, commissioning, preventive maintenance, hardware troubleshooting, repair, and technical training. You will be responsible for sustaining optimal instrument performance, driving high customer satisfaction, and supporting the reliable operation of genomic testing and research workflows—this is not purely a desk-based role, but a dynamic position requiring field execution and technical problem-solving. Key Measures Of Success • On-time instrument installation & commissioning with zero critical post-installation defects, • High instrument uptime & fast resolution of hardware-related technical faults, • Strong customer satisfaction scores and long-term customer loyalty, • Effective knowledge transfer to distributor service teams and end-user technicians, • Accurate & compliant service documentation, including maintenance records and repair reports, • Proactive preventive maintenance execution to minimize unplanned downtime Position Responsibilities • Prepare comprehensive materials, documentation, and packaging for instrument installation, on-site commissioning, and after-sales maintenance, ensuring full readiness for all service activities., • Evaluate required supplies, components, and checklists for product demonstrations, coordinate preparation efforts, and follow through to guarantee flawless demo execution., • Deliver responsive hardware technical support and maintenance services for customers post-sale, conducting both on-site and remote troubleshooting to resolve malfunctions efficiently., • Design and deliver structured technical training for distributor Field Service Engineers and customer laboratory staff, building their capability to operate and maintain instruments independently., • Perform routine on-site inspections to assess instrument operating status, proactively identify potential issues, and assist customers in maintaining consistent, reliable instrument performance., • Maintain detailed, accurate service records, project documents, and technical reports in compliance with company policies and quality management standards., • Collaborate cross-functionally with sales, application, and R&D teams to share customer feedback, resolve complex technical issues, and improve overall product reliability and customer experience. Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs. Position Requirements • Bachelor’s degree or above in Automation, Electronics, Electrical Engineering, Semiconductor, Mechatronics, or related technical disciplines., • 3+ years of hands-on hardware maintenance experience in medical devices, precision analytical instruments, or life science equipment., • Proficiency in instrument assembly, disassembly, circuit troubleshooting, mechanical calibration, and hardware fault resolution for high-precision equipment., • Excellent verbal communication skills, with the ability to draft clear, compliant project documents, service reports, and technical records independently., • Strong learning agility and adaptability, with the ability to quickly master complex genomic sequencing instruments and emerging technical knowledge., • Good oral English proficiency; fluent English skills are highly preferred to support global customers and cross-regional collaboration., • Willing and able to travel frequently domestically and internationally as required to fulfill service obligations., • Customer-focused mindset, strong sense of responsibility, attention to detail, and professional work ethic with a commitment to quality service. All listed requirements are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities. Preferred Experience & Skills • Prior experience servicing NGS sequencers, PCR instruments, or other laboratory genomic/analytical equipment is strongly preferred., • Experience delivering technical training, supporting distributor service teams, or managing multi-site service operations., • Familiarity with medical device quality systems, including ISO13485, GMP, or relevant regulatory compliance standards., • Advanced hands-on expertise with electrical, mechanical, and optical components of precision laboratory instruments., • Experience supporting global customers or cross-cultural technical collaboration., • Proactive problem-solving skills and ability to work independently with minimal supervision in field settings. Who We Are GeneMind is a leading global innovator and manufacturer of next-generation sequencing (NGS) systems, powered by independent core intellectual property. We develop and deliver high-performance, reliable sequencing solutions to empower precision medicine, scientific research, and public health initiatives worldwide. We are deeply committed to fostering an inclusive, supportive workplace that values diversity, professional growth, and collaborative innovation. We prioritize employee development, encourage curiosity, and empower every team member to make a meaningful impact on our mission to advance genomic technology for global health equity. Equal Opportunity Employer: We celebrate diversity and are committed to creating an inclusive environment for all employees. We provide equal employment opportunities without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

¡Ampliamos nuestro equipo! 🔎 ¿Buscas un nuevo reto donde desarrollar tu carrera y aprender nuevas tecnologías? Entonces sigue leyendo porque esto te puede interesar. Scalian es una empresa de más de 6.000 personas con una dimensión internacional, con oficinas en Europa y América del Norte. Estamos especializados en dar servicios a diferentes clientes enfocados en Data, Cloud e Inteligencia Artificial. ¿Qué buscamos? Buscamos un/a profesional con experiencia en el sector industrial, para colaborar en la mejora del rendimiento y la capacidad productiva de un proveedor. La misión principal será ayudar a un supplier a alcanzar los niveles de producción planificados, trabajando de forma presencial en sus instalaciones y coordinando con el Tier 1 y el propio proveedor. Requisitos mínimos: • Experiencia de al menos 2 años en entornos industriales (Supply Chain y/o Calidad)., • Experiencia en "Transfers of Work" o trasferencias de trabajo, • Experiencia en sector aeroespacial será positivamente valorado, • Nivel alto de inglés hablado y escrito ¿Qué tendrás con nosotros? ⛱ 25 días laborables de vacaciones 💻 Teletrabajo 📝 Contrato indefinido 📚 Formación continua, certificaciones, meetups y planes de desarrollo profesional personalizados para que podamos seguir creciendo juntos. Contamos con acceso a plataformas internas con contenido abierto para que lo disfrutes cuando tú quieras y a tu ritmo. 🕐 Jornada completa con horario flexible para facilitar la conciliación entre vida familiar y profesional. 🎉 After works en las oficinas 🎂 La tarde del cumpleaños libre 🏋️ ♀️ Descuentos en gimnasios 💲Programas de retribución flexible: seguro médico, tarjeta restaurante, abono de transporte, cheques para escuelas infantiles. ⚖️ En Scalian valoramos la diversidad e impulsamos un entorno de trabajo inclusivo, donde todas las personas, independientemente de su género, identidad, edad o procedencia, puedan desarrollarse profesionalmente. 🌏 Como parte del grupo Scalian, abrimos nuestras fronteras y crecemos internacionalmente. ♻️ En el grupo apostamos por iniciativas sostenibles. ¡Despega en tu carrera con Scalian Spain!✈

Davidson Consulting España nace en el año 2014. Formamos parte del grupo Davidson, multinacional francesa de servicios tecnológicos con +18 años de experiencia en el sector y presencia en varios países europeos además de en Canadá. Somos 3000 compañeros a nivel global. Desde Davidson buscamos un/a Ingeniero de Calidad de Proveedores Avanzado (ASQ), para unirse a nuestro equipo en Pamplona, que asegure la calidad de los componentes y el correcto despliegue de los procesos de calidad junto a nuestros equipos internos y proveedores. Funciones: • Liderar el despliegue del proceso APQP (Advanced Product Quality Planning) durante el desarrollo e industrialización de nuevos productos., • Asegurar la correcta definición, traducción y trazabilidad de los Critical to Quality (CTQ) establecidos por Ingeniería en las especificaciones técnicas., • Garantizar que los requisitos críticos de calidad son comprendidos y compartidos por todos los stakeholders, incluyendo los proveedores., • Coordinar y dinamizar los análisis de riesgos y las actividades de APQP con equipos internos y externos., • Trabajar estrechamente con Ingeniería, Diseño, Industrialización y proveedores para asegurar el cumplimiento de los requisitos de calidad., • Evaluar los entregables del PPAP (Production Part Approval Process) y verificar que los CTQ están correctamente controlados. Requisitos mínimos del puesto: • Licenciatura en Ingeniería o equivalente en Ingeniería Mecánica o Calidad Industrial., • + 5 años en entornos industriales. Experiencia técnica (diseño, métodos o industria) con componentes mecánicos, complementada con experiencia en calidad., • Conocimiento de procesos de fabricación de componentes mecánicos., • Valorable la experiencia en la industria automotriz y en procesos APQP., • Valorable la experiencia en auditorías de procesos VDA., • Organización y liderazgo para desafiar equipos de proyectos y proveedores. Manejo simultáneo de 30-70 componentes., • Inglés fluido. ¿Qué ofrecemos? • Modelo de trabajo en formato presencial. Lugar de residencia Pamplona., • Contratación indefinida., • Salario competitivo según valía y experiencia aportada., • Plan de carrera y desarrollo profesional. ¿Por qué unirte a nosotros? Nos caracterizamos por el excelente trato a los compañeros y una estructura organizativa horizontal. Te sentirás arropado y como en casa, tu opinión siempre importa. Contarás con oportunidades reales de crecimiento y proyección. Si estás interesad@ en participar en el proceso de selección o simplemente quieres conocer más sobre estas oportunidades, ¡no dudes en postularte a la oferta! #DavidsonConsulting #TeRetamosAFicharPorNosotros

This position requires frequent travel to customer manufacturing plants located across Spain to support MES implementations, commissioning, troubleshooting, and production operations. MES (Manufacturing Execution Systems) Controls Engineer The MES Controls Engineer is responsible for supporting and optimizing manufacturing execution and automation systems in a high‑volume discrete manufacturing environment, with an emphasis on real‑time shop‑floor execution, seamless ERP (Enterprise Resource Planning) –MES–PLC (Programmable Logic Controller) integration, and sustained production reliability under strict uptime and quality requirements. CORE RESPONSIBILITIES · Provide support for MES–PLC integrations during system launches and periods of constrained production. · Configure, establish, and maintain MES-to-PLC communications · Integrate MES template routines and user-defined data types (UDTs) into PLC programs. · Assign, modify, and maintain PLC tags and logic required to send/receive MES transactions. · Collaborate with Process Engineers and the MES team to understand process scope and ensure proper MES integration. · Document all MES-related PLC changes and issues on production lines and communicate updates in a timely manner. · Troubleshoot PLC, HMI (Human Display Interface), and industrial network issues affecting MES execution. · Ensure accuracy of real-time production reporting through MES. · Support resolution of production execution issues impacting throughput or quality. · Partner with supervisors and operators to support effective MES workflows. · Support quality enforcement and validation through MES. · Collaborate with Process Engineering to manage part numbers and part number groups within the MES system. · Assist with MES-related audits, investigations, and data requests. · Identify and recommend MES process and system improvement opportunities. · Support MES enhancements, system upgrades, and production rollouts. QUALIFICATIONS · Bachelor’s degree in engineering or a related technical discipline · 5+ years of hands‑on experience with Allen‑Bradley/Rockwell and Siemens tag‑based PLC and HMI systems. · Strong PLC and HMI troubleshooting and diagnostic skills. · Basic understanding of Manufacturing Execution Systems (MES) preferred. The MES Controls Engineer is responsible for supporting and optimizing manufacturing execution and automation systems in a high‑volume discrete manufacturing environment, with an emphasis on real‑time shop‑floor execution, seamless ERP (Enterprise Resource Planning) –MES–PLC (Programmable Logic Controller) integration, and sustained production reliability under strict uptime and quality requirements. CORE RESPONSIBILITIES · Provide support for MES–PLC integrations during system launches and periods of constrained production. · Configure, establish, and maintain MES-to-PLC communications · Integrate MES template routines and user-defined data types (UDTs) into PLC programs. · Assign, modify, and maintain PLC tags and logic required to send/receive MES transactions. · Collaborate with Process Engineers and the MES team to understand process scope and ensure proper MES integration. · Document all MES-related PLC changes and issues on production lines and communicate updates in a timely manner. · Troubleshoot PLC, HMI (Human Display Interface), and industrial network issues affecting MES execution. · Ensure accuracy of real-time production reporting through MES. · Support resolution of production execution issues impacting throughput or quality. · Partner with supervisors and operators to support effective MES workflows. · Support quality enforcement and validation through MES. · Collaborate with Process Engineering to manage part numbers and part number groups within the MES system. · Assist with MES-related audits, investigations, and data requests. · Identify and recommend MES process and system improvement opportunities. · Support MES enhancements, system upgrades, and production rollouts. QUALIFICATIONS · Bachelor’s degree in engineering or a related technical discipline · 5+ years of hands‑on experience with Allen‑Bradley/Rockwell and Siemens tag‑based PLC and HMI systems. · Strong PLC and HMI troubleshooting and diagnostic skills. · Basic understanding of Manufacturing Execution Systems (MES) preferred.

3PBioViAn is seeking a Head of QA (Audits, Inspections, Suppliers and Plant) to lead the internal audit program, supplier qualification activities, and GMP/compliance initiatives. You will drive audit execution, CAPA, and inspections readiness to support regulatory inspections including FDA inspections. The role requires advanced English (C1), a Life Sciences degree (Masters desirable), and 3–4 years in QA within pharma/biotech. Located in Navarre, relocation support offered for outside Navarra. #J-18808-Ljbffr

Davidson Consulting España nace en el año 2014. Formamos parte del grupo Davidson, multinacional francesa de servicios tecnológicos con +18 años de experiencia en el sector y presencia en varios países europeos además de en Canadá. Somos 3000 compañeros a nivel global. Desde Davidson buscamos un/a Ingeniero de Calidad de Proveedores Avanzado (ASQ), para unirse a nuestro equipo en Pamplona, que asegure la calidad de los componentes y el correcto despliegue de los procesos de calidad junto a nuestros equipos internos y proveedores. Funciones: • Liderar el despliegue del proceso APQP (Advanced Product Quality Planning) durante el desarrollo e industrialización de nuevos productos., • Asegurar la correcta definición, traducción y trazabilidad de los Critical to Quality (CTQ) establecidos por Ingeniería en las especificaciones técnicas., • Garantizar que los requisitos críticos de calidad son comprendidos y compartidos por todos los stakeholders, incluyendo los proveedores., • Coordinar y dinamizar los análisis de riesgos y las actividades de APQP con equipos internos y externos., • Trabajar estrechamente con Ingeniería, Diseño, Industrialización y proveedores para asegurar el cumplimiento de los requisitos de calidad., • Evaluar los entregables del PPAP (Production Part Approval Process) y verificar que los CTQ están correctamente controlados. Requisitos mínimos del puesto: • Licenciatura en Ingeniería o equivalente en Ingeniería Mecánica o Calidad Industrial., • + 5 años en entornos industriales. Experiencia técnica (diseño, métodos o industria) con componentes mecánicos, complementada con experiencia en calidad., • Conocimiento de procesos de fabricación de componentes mecánicos., • Valorable la experiencia en la industria automotriz y en procesos APQP., • Valorable la experiencia en auditorías de procesos VDA., • Organización y liderazgo para desafiar equipos de proyectos y proveedores. Manejo simultáneo de 30-70 componentes., • Inglés fluido. ¿Qué ofrecemos? • Modelo de trabajo en formato presencial. Lugar de residencia Pamplona., • Contratación indefinida., • Salario competitivo según valía y experiencia aportada., • Plan de carrera y desarrollo profesional. ¿Por qué unirte a nosotros? Nos caracterizamos por el excelente trato a los compañeros y una estructura organizativa horizontal. Te sentirás arropado y como en casa, tu opinión siempre importa. Contarás con oportunidades reales de crecimiento y proyección. Si estás interesad@ en participar en el proceso de selección o simplemente quieres conocer más sobre estas oportunidades, ¡no dudes en postularte a la oferta! #DavidsonConsulting #TeRetamosAFicharPorNosotros

This role is for an experienced Field Application Engineer with technical knowledge of Fluke Industrial Products and the applications these products are used in. The Field Application Engineer will enable the local sales team to drive growth for the selected Fluke products in the region. They will be the technical go-to expert for the selected products and will provide pre-and post-sales technical support for distributors, end-customers and the local sales teams. • Support the local sales team and customers with application, technical and competitive information, • Provide Pre & Post sales technical support to our field sales team, distribution channels and end users, • Develop technical skills through training provided by product experts, self-learning on the job and liaising with factory-based technical support engineers, • Provide sales support at shows, conferences, seminars and roadshows; be able to prepare and deliver presentations and product demonstrations virtually and on-site, • Develop training programs for both online and classroom delivery, • Work with Fluke’s CRM (Microsoft Dynamics Software) to record customer communications and track opportunities, • Assist EMEA sales and marketing team with New Product Introductions (NPIs), • Work with EMEA team and Sales Program Managers to develop ideas for regional marketing activities, • Provide technical assistance to Inside Sales team, • Strong proven technical product and application knowledge preferably on the Fluke Products or with Industrial Test and Measurement products, • Able to present and demonstrate measurement solutions to end users, • Able to communicate and motivate via different media platforms., • Understands the principles of sales and solutions selling., • Build relationship with key customers based on technical knowledge., • Ability to work effectively in a cross-functional team environment, • A high level of independence and ability to “self-educate”., • Fluent in Spanish and English., • Knowledge of additional languages ( Portuguese, Italian) is highly valued. Fortive's essential technology makes the world safer and more productive. We accelerate transformation in high-impact fields like workplace safety, build environments, and healthcare. We are a global industrial technology innovator with a startup spirit. Our forward-looking companies lead the way in healthcare sterilization, industrial safety, predictive maintenance, and other mission-critical solutions. We're a force for progress, working alongside our customers and partners to solve challenges on a global scale, from workplace safety in the most demanding conditions to advanced technologies that help providers focus on exceptional patient care. We are a diverse team 10,000 strong, united by a dynamic, inclusive culture and energized by limitless learning and growth. We use the proven Fortive Business System (FBS) to accelerate our positive impact. At Fortive, we believe in you. We believe in your potential—your ability to learn, grow, and make a difference. At Fortive, we believe in us. We believe in the power of people working together to solve problems no one could solve alone. At Fortive, we believe in growth. We're honest about what's working and what isn't, and we never stop improving and innovating. Fortive: For you, for us, for growth. Fluke is leading the world in creating software, test tools and technology that will support customers today and in the future. We are a customer-obsessed market leader with a strong reputation for reliability, quality and safety.A wholly owned subsidiary of Fortive Corporation (www.fortive.com), Fluke is a global corporation headquartered in the greater Seattle area. Driven by the successful Fortive Business System, Fluke offers the passion of a startup with the resources of a Fortune 500 company. We are focused on the growth of our individual employees, teams and the Fluke brand. We Are an Equal Opportunity Employer. Fortive Corporation and all Fortive Companies are proud to be equal opportunity employers. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity or expression, or other characteristics protected by law. Fortive and all Fortive Companies are also committed to providing reasonable accommodations for applicants with disabilities. Individuals who need a reasonable accommodation because of a disability for any part of the employment application process, please contact us at applyassistance@fortive.com. #J-18808-Ljbffr

We are working on a Senior Womenswear Fashion Design Manager on behalf of a leading international fashion retail business based in Kuwait. This is an exciting opportunity to join a design-led organisation that continues to invest heavily in product innovation, brand development and international growth. Working as part of an established creative team, the successful candidate will play a central role in shaping seasonal womenswear collections for a broad and discerning customer base. THE POSITION WILL REQUIRE RELOCATION TO KUWAIT The Role The Senior Fashion Designer will be responsible for developing commercially successful collections from concept through to final product, combining strong creative vision with an in-depth understanding of customer trends and market dynamics. Working closely with buying, merchandising and sourcing teams, you will ensure collections are delivered on time, within budget and in line with the overall brand direction. Key Responsibilities Design and develop seasonal womenswear collections across multiple product categories. Research global fashion, consumer and lifestyle trends to identify new opportunities. Produce mood boards, colour palettes, fabric selections and design concepts. Collaborate closely with buying, technical and production teams throughout the product development cycle. Work with suppliers and manufacturers to ensure design integrity and quality standards are maintained. Attend fit sessions, review samples and oversee collection refinement through to final sign-off. Support the development of a strong and differentiated product identity aligned to the brand strategy. Candidate Profile Proven experience as a Senior Fashion Designer within a premium or high-volume fashion retail environment. Recent experience with an internationally recognised retailer. Strong understanding of womenswear product development, fabric sourcing and commercial design. A creative eye combined with excellent technical and product development capabilities. Ability to balance innovation with commercial awareness and customer insight. Confident communicator, capable of working effectively across international teams and supplier networks. Package Competitive tax-free salary and benefits package. Relocation assistance where required. Long-term opportunity to contribute to the growth of an ambitious and well-invested international fashion group.

We are working on a Senior Womenswear Fashion Design Manager on behalf of a leading international fashion retail business based in Kuwait. This is an exciting opportunity to join a design-led organisation that continues to invest heavily in product innovation, brand development and international growth. Working as part of an established creative team, the successful candidate will play a central role in shaping seasonal womenswear collections for a broad and discerning customer base. THE POSITION WILL REQUIRE RELOCATION TO KUWAIT The Role The Senior Fashion Designer will be responsible for developing commercially successful collections from concept through to final product, combining strong creative vision with an in-depth understanding of customer trends and market dynamics. Working closely with buying, merchandising and sourcing teams, you will ensure collections are delivered on time, within budget and in line with the overall brand direction. Key Responsibilities Design and develop seasonal womenswear collections across multiple product categories. Research global fashion, consumer and lifestyle trends to identify new opportunities. Produce mood boards, colour palettes, fabric selections and design concepts. Collaborate closely with buying, technical and production teams throughout the product development cycle. Work with suppliers and manufacturers to ensure design integrity and quality standards are maintained. Attend fit sessions, review samples and oversee collection refinement through to final sign-off. Support the development of a strong and differentiated product identity aligned to the brand strategy. Candidate Profile Proven experience as a Senior Fashion Designer within a premium or high-volume fashion retail environment. Recent experience with an internationally recognised retailer. Strong understanding of womenswear product development, fabric sourcing and commercial design. A creative eye combined with excellent technical and product development capabilities. Ability to balance innovation with commercial awareness and customer insight. Confident communicator, capable of working effectively across international teams and supplier networks. Package Competitive tax-free salary and benefits package. Relocation assistance where required. Long-term opportunity to contribute to the growth of an ambitious and well-invested international fashion group.

About the company ChemScene is a global leading manufacturer and supplier of building blocks and fine research chemicals. Our mission is to pave the way for drug discovery by providing the most innovative chemicals with the highest-level quality for a reasonable price. What we offer Our commitment is to establish an inclusive, harmonious, and efficient workplace, providing ample opportunities for every employee to grow and reach their full potential. As a global company, we actively seek out talent from all corners of the world to enhance localization in our workforce. At ChemScene, we continuously explore new avenues, providing you the freedom to pursue your goals. Our diverse range of businesses allows for multiple career paths to explore new horizons. We welcome you to join us! Sales Manager Location-based While this is a remote role with a Spain scope, the ideal candidate should be open to traveling to client locations as required. Your role The following work will be carried out by Sales role on behalf of the ChemScene: • Work independently to achieve sales growth target and reach sales goal in your responsible sales region in Spain., • Promote ChemScene brand and products in the responsible sales region in Spain., • Interact well with customers and maintain good customer relationships, visit customers regularly, develop new customers, being professional and courteous. Reach weekly target number of field visit and leads prospecting., • Communicate accurate information regarding products, prices, product availability, and current promotions to customers. Professionally contact customers via phone call, chats and emails regarding orders and technical questions., • Customer inquiries follow-up, register ChemScene Spain entity into customer’s procurement system, tender project follow-up., • Work as an effective team player to ensure the highest level of efficiency and success for the team., • Represent ChemScene as an exhibitor at academic conferences, exhibitions and vendor shows to increase brand awareness and expand market share over local market, • Involved in other activities related to ChemScene sales & marketing activities, other relevant tasks allocated by reporting supervisor. Required Skills • Bachelor's degree or higher in Chemistry, Organic Chemistry, Biochemistry, or other related fields., • Familiarity with the chemical or biopharmaceutical industry and at least three years of sales experience., • Willingness to work in sales and ability to handle a certain level of job pressure., • Friendly, outgoing, open-minded, and strong sense of responsibility., • Strong communication skills, a proactive attitude, and a good customer service orientation., • Fluent in both spoken and written Spanish and English., • High self-motivation and perseverance., • Prior customer resources in the Spain sales region are a plus. What you will get in return • Full support from the EU team., • Comprehensive training package., • Base salary plus sales commission. Please submit a cover letter and resume to apply for this position (MS Word or pdf files). Company’s website: https://www.chemscene.com/

We are looking for a QA Specialist (QC Laboratory) to join our Quality Assurance Team. As QA Specialist (QC Laboratory), your responsibilities will include: • Act as the Quality Assurance representative within the Quality Control laboratory, ensuring compliance with GMP regulations and quality standards., • Provide active QA on-the-floor support, ensuring immediate quality guidance and promoting GMP and documentation best practices across laboratory activities., • Perform critical review of analytical documentation, laboratory records, calculations, chromatograms, integrations, analytical results and raw data., • Ensure Data Integrity compliance following ALCOA+/ALCOA++ principles, guaranteeing traceability, reliability, availability and integrity of both electronic and paper-based records., • Oversee GMP-compliant use of laboratory computerized systems and equipment, including LIMS, Empower 3, Gen 5 and other analytical platforms., • Review user access management, audit trails, backups and data archival processes whenever applicable., • Participate in deviation investigations, root cause analysis, impact assessments and CAPA definition, implementation and effectiveness verification., • Prepare, review and improve SOPs related to Quality Control, Data Integrity, raw data management, computerized systems and audit trail reviews., • Support the qualification and training of laboratory personnel in GMP requirements, Data Integrity principles and Good Documentation Practices., • Support analytical method validation and transfer activities, ensuring compliance with applicable regulatory requirements., • Collaborate closely with QC, QA, IT, Validation and other cross‑functional departments to maintain a culture of quality and continuous improvement., • Bachelor’s degree in Chemistry, Biotechnology, Biology, Biochemistry, Pharmacy or other related scientific discipline., • Minimum 4 years of experience in QA, QC or equivalent roles within a GMP-regulated pharmaceutical or biotechnology environment., • Proven experience in raw data review, analytical results verification, deviation investigations, CAPA management and GMP documentation., • Strong knowledge of GMP requirements, Good Documentation Practices and Data Integrity principles., • Working knowledge of EU GMP Annex 11, FDA 21 CFR Part 11 and GAMP 5 regulations., • Experience with laboratory computerized systems such as LIMS, Empower 3 and/or Gen 5., • Knowledge of analytical techniques including HPLC, UPLC, UV, IR, ELISA and microbiological/biological methods., • Experience in analytical method transfer and validation activities will be highly valued., • Master’s degree or postgraduate qualification in Quality, Pharmaceutical Industry, Computerized Systems Validation (CSV) or Data Integrity will be considered an asset., • Spanish fluent and English B2/C1 level, with the ability to review GMP documentation in English., • Previous experience in biotechnology/CDMO environments working with recombinant proteins, monoclonal antibodies, biosimilars, ADCs or other biologics will be highly valued., • You will have 26 paid days off: 23 vacation days + 2 personal days + 1 day off set by the company., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income tax (childcare, health insurance, training, etc.)., • Company benefits club, which allows 3P employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, Fnac, Rituals, El Corte Inéls, etc.)., • Flexible working hours during the week and a reduce work day on Friday of 7h., • Special Summer working day of 7h during July and August., • 3PBio is committed to the continuous, updated and personalized improvement of our personnel’s learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision‑making processes., • All new hires who reside outside of Navarra are provided with a relocation service and/or assistance. We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and cGMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human an animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. #J-18808-Ljbffr

Job Overview We are looking for a country manager with entrepreneurial spirit and strong results orientation, responsible for building and leading the company's business in the EU region from scratch. This is a unique high-impact position suitable for sales leaders who crave challenges and autonomy. You will be responsible for developing market entry strategies, establishing key partnerships, building high-performance sales teams, and driving significant revenue growth. Your success will be directly rewarded through an unlimited commission structure. Main responsibilities • Partnership Development: Proactively identify, approach, and build strong relationships with strategic partners, affiliates, communities, and key opinion leaders (KOLs). Maintain high outreach velocity and continuously expand a quality partner network., • Business Growth & KPI Achievement: Drive regional performance by improving key commercial metrics related to customer acquisition, engagement, and overall revenue contribution. Deliver measurable business impact through disciplined execution and performance tracking., • Full BD Process Ownership: Independently manage the entire BD lifecycle - prospecting, qualification, negotiation, follow-ups, closing, and post-deal maintenance. Ensure fast execution and a healthy pipeline., • Client & Partner Relationship Management: Build and maintain long-term, trust-based relationships with partners. Increase engagement, retention, and contribution through proactive and high-frequency communication., • Market Research & Competitive Insights: Monitor regulatory updates, competitor strategies, user behaviour, and market dynamics in the EU region. Provide actionable insights and identify new partnership opportunities., • Localized Marketing Collaboration: Work closely with marketing teams to support localized content, community engagement, and event initiatives. Ensure smooth and effective execution across Spanish-speaking markets.re all sales and partnership activities comply with local regulations and company policies. Job requirements (must be met) • Minimum 2-3 years of experience in sales or business development, capable of independently acquiring and converting clients., • Strong execution, self-discipline, and ability to work effectively in a remote, fast-paced environment., • Excellent communication skills with the ability to maintain long-term relationships and manage high-frequency partner interactions., • Good command of English and Spanish for business communication (Mandarin proficiency is a strong plus)., • High resilience and emotional stability under pressure and rejection., • Existing partner, affiliate, community, or KOL resources that can contribute value in the short term., • Experience in digital platforms, online services, fintech, or other performance-driven industries, or strong personal familiarity with similar ecosystems., • Strong hunter mindset: bonus-driven, results-oriented, and motivated by performance-based outcomes. We provide • Uncapped Income Potential: An attractive compensation package that includes a generous base salary and more importantly an uncapped commission structure that directly rewards your performance., • Autonomy and Influence: Freedom to form your own team and develop strategies for the entire region. Your decisions will directly affect the global success of the company., • Career Development: This is a senior leadership position where you will have great career and financial advancement opportunities as the company grows., • Global Environment: Work with a diverse international team to serve customers worldwide., • Remote work flexibility: can work from anywhere in the world.

About Us HBX Group is a leading B2B ecosystem player in the TravelTech space, connecting and empowering businesses in the ever-evolving world of travel. We drive growth for our clients and partners while removing friction from the end-to-end travel experience. Our cloud-based technology platforms offer fast and reliable access to a unique portfolio of travel products & services, while rich data and intelligence seamlessly connect supply and demand worldwide. Job Summary We are looking for a Corporate Strategy Manager to play a pivotal role in shaping and delivering the Group’s strategic priorities. Partnering closely with the Head of Corporate Strategy and senior leadership, this role combines rigorous analytical thinking with strong synthesis and executive-level presentation skills to develop materials that directly influence key strategic decisions at executive, board, and investor levels. You will help define the company’s long‑term vision and strategic pillars, informed by deep market expertise and understanding of the competitive landscape while elevating the quality and consistency of strategic planning across the organization. This is a high‑impact role suited for candidates with a strong background in strategy consulting or equivalent strategic roles in complex, fast‑moving environments. The position is remote within Spain, with the option to work hybrid from Mallorca for those planning or willing to relocate. Job Responsibilities Support Group Strategy Definition & Strategic Planning • Partner with the Head of Corporate Strategy to drive the strategy definition and management agenda, including multi‑year plans (e.g. 3YP)., • Build a robust strategic fact base through deep analysis of market trends, competitive dynamics, internal performance, and emerging risks and opportunities., • Co‑define strategic pillars and objectives with senior leadership to guide prioritization and initiative design., • Establish and maintain a clear strategy planning framework, ensuring cross‑functional alignment with Finance, Commercial Strategy, and Commercial Planning & Performance. Lead Market Insights & Intelligence (Market Lighthouse) • Develop and continuously update proprietary ecosystem market models (e.g. Accommodation, M&E) to size and identify segmented growth opportunities., • Lead primary research through direct engagement with clients, suppliers, external experts, and internal stakeholders across Sales, Sourcing, Product, and Finance., • Produce competitive landscape analyses covering strategic positioning, growth, profitability, and market share to inform commercial and strategic actions., • Deliver regular market and industry updates to senior management and Board. Shape Strategic Discoveries & Growth Opportunities • Identify and assess new business and diversification opportunities (e.g. adjacent services, new verticals, emerging business models)., • Monitor and interpret industry and competitor shifts (e.g. pricing pressure, margin trends, consolidation) to support timely executive decisions. Skillset and Experience Required • Minimum 5 years of relevant experience in strategy consulting and/or corporate strategy roles within complex, international organizations., • Full professional proficiency in English is essential; additional languages are a plus., • Strong strategic leadership and problem‑solving capabilities, with experience leading complex, high‑visibility initiatives in ambiguous, fast‑moving environments., • Outstanding analytical rigor and financial acumen, including market and competitive analysis, business cases, P&L modeling, and quantitative strategic planning., • Exceptional synthesis, storytelling, and presentation skills, with a proven ability to translate complex data into clear, actionable insights for senior and executive audiences., • Highly collaborative and influential operator, able to manage multiple priorities, build strong cross‑functional relationships, and influence outcomes without formal authority. At HBX Group, we believe that diversity drives innovation and makes travel a force for good. We're committed to creating an inclusive workplace where everyone feels valued and respected, embracing different backgrounds, perspectives and talents. Join us and be part of a team where diversity and equal opportunities really do make a difference.

🛠️ Now Hiring: Senior Data Modeller / Data Integration Developer | B2B Contract | Spain, Remote We are looking for a Senior Data Modeller / Data Integration Developer to design and implement data architecture, data models, integration solutions, and data quality processes across enterprise data platforms. 📍 Location: Spain Remote 💼 Employment Type: B2B Contract 🎯 Experience: 5–10+ years 🔍 What You’ll Bring: 🔹 Strong experience in Data Architecture, Data Modelling & Data Engineering 🔹 Experience translating business requirements into data and engineering specifications 🔹 Hands-on experience developing, coordinating and maintaining data models 🔹 Experience with solution architecture, design and implementation of data-driven products 🔹 Strong experience in large-scale data migration and Big Data on-premise environments 🔹 Experience integrating Data Science platforms such as Dataiku 🔹 Strong hands-on experience with Docker & Kubernetes 🔹 Good knowledge of distributed query engines such as Presto / Trino 🔹 Experience with Hadoop, Hive, HBase, Spark, Solr, Tez, Kafka 🔹 Experience with orchestration tools such as Apache Airflow / NiFi 🔹 Strong understanding of Data Quality standards, policies and processes 🔹 Expert-level SQL skills across traditional DWH and distributed data environments 🔹 Python automation and troubleshooting experience using Jupyter Notebooks / common IDEs 🔹 Experience preparing data for reporting, analytics and visualization using Tableau, Power BI or Python 🔹 Knowledge of Agile methodologies – Scrum / SAFe 🔹 Banking or Financial Services data experience is highly advantageous 🔹 Excellent communication and stakeholder management skills 🔹 German language skills are beneficial 🔗 Let’s Connect: 📩 DM me on LinkedIn to explore this opportunity. 📧 Send your CV to: Please feel free to share this opportunity with your network if you know someone who could be a good fit

Select how often (in days) to receive an alert: REQUISITION ID: 12870 LOCATION: Sarriguren, ES, 31621 Madrid, M, ES, 28001 As part of our growth we are looking for a Senior Power Platform & Data Solutions Lead. In this role, this person will maintain, support and further evolve the Microsoft Power Platform and data solutions ecosystem used to manage the global Engineering project and resource portfolio. The role combines hands-on solution development, data modelling, process automation, advanced analytics, reporting and technical leadership for digitalization initiatives across Engineering and adjacent business functions. You will perform the following tasks: YOUR TASKS: • Maintain, support and continuously improve existing Power Platform-based business applications, automations and reporting solutions, • Lead the technical implementation of new digitalization initiatives across Engineering and adjacent functions such as Finance, R&D and Operations, including:, • Business application design and development, • Dataverse data modelling and data governance, • Integration with Microsoft Planner Premium and other enterprise data sources (ERP/PLM), • Process automation using Power Automate, • Power BI reporting, semantic models and advanced analytics, • Troubleshooting, documentation and contribution to application lifecycle management practices, • Collaborate with global stakeholders across Spain, Germany, India and other international locations, providing technical guidance, user support and training when required, • Coordinate external IT service providers supporting the department’s digital solutions, ensuring proper follow-up, service quality and alignment with business needs YOUR PROFILE: • Bachelor’s* or Master’s degree in Engineering, Computer Science, Information Systems, Data Analytics, Business Intelligence, Software Engineering, Telecommunications, Mathematics, Physics or a comparable field, • Minimum 5–7 years of professional experience in business applications, data analytics, BI, process automation or similar fields, including at least 3 years of hands-on experience with Microsoft Power Platform, • Specialization in the Microsoft Power Platform technology stack will be highly valued. Microsoft certifications related to Power Platform, Azure, Data, AI or Microsoft 365 will be considered an advantage, particularly PL-400, PL-200, PL-600, DP-600 or equivalent certifications, • Proven proficiency and hands‑on experience in the end‑to‑end design, development, deployment and maintenance of Power Platform solutions, including Power Apps, Dataverse, Power Automate,Power BI and advanced Excel, • Strong analytical mindset, structured communication skills and ability to translate business needs into scalable technical solutions. The candidate should be autonomous, proactive, well organized and comfortable working in an international environment., • Experience with AI, big data, Microsoft Fabric, Python, machine learning or advanced analytics will be considered a plus, • Fluent in English. Spanish & German would be a plus *For foreign qualifications, recognition as the corresponding Spanish degree equivalency is required when applying. YOUR BENEFITS In addition to the opportunity to make our world a little more sustainable, we offer you: *Some offers may varyby location Nordex adheres to a policy of equal employment opportunity. All employment decisions are made without regard to religion, age, sex, color, national origin, handicap, or other protected class and are in full compliance with all federal and state laws. Recruitment Fraud Notice:Please note that our People Attraction department will only contact youvia official @nordex-online.com email addresses or authorized recruitment partners.You can find more information about our application processon our website. The manufacture of wind energy plants in the on-shore segment has been our core competence and passion for around 40years. With more than 57GW installed capacity worldwide, our turbines supply sustainable energy to more than 80% of the global energy market and we are one of the largest companies in the wind industry. National subsidiaries in more than 40markets and production facilities in Germany, Spain, Brazil, the USA, Mexico and India offer our more than 10,400employees the opportunity for international and intercultural cooperation. We are growing and together driving forward the expansion of alternative energies worldwide - if you wish, from now on with you. Join the #TeamNordex #J-18808-Ljbffr

We are looking for a Head of QA (Audits, Inspections, Suppliers and Plant) to join our Quality Assurance Team. In this role, you will be responsible for managing, coordinating, and executing the company's internal audit program, supplier qualification activities, and compliance initiatives. You will play a key role in ensuring the Quality Management System remains compliant with GMP requirements and supports successful regulatory inspections, including FDA inspections. As Head of QA (Audits, Inspections, Suppliers and Shop Floor), your responsibilities will include: • Develop and execute the company's internal audit plan aligned with quality and compliance objectives., • Lead and coordinate internal audits across the organization., • Design and manage supplier qualification and monitoring programs., • Execute supplier qualification audits and assessments., • Monitor and analyze quality KPIs and performance indicators., • Identify, investigate, and elevate GMP non-conformities when appropriate., • Lead and support compliance improvement projects., • Participate in regulatory inspections, customer audits, and mock inspections., • Contribute to FDA inspection readiness and follow-up activities., • Collaborate with cross-functional teams to ensure adherence to quality standards and regulatory requirements., • Support company integration initiatives and quality improvement projects., • Ensure effective implementation of corrective and preventive actions (CAPA)., • Bachelor's degree in Biology, Biochemistry, Chemistry, Pharmacy, or a related Life Sciences field., • Master's degree in a relevant scientific discipline is highly desirable., • 3-4 years of experience within a Quality Assurance environment in the pharmaceutical, biotech, or healthcare industry., • Strong knowledge of GMP regulations and Quality Management Systems., • Experience conducting internal audits and supplier qualification activities., • Exposure to FDA inspections is considered a strong advantage., • Experience managing compliance and continuous improvement projects., • Advanced English level (C1 or equivalent) is required., • Additional languages are a plus., • You will have 26 paid days off: 23 vacation days + 2 personal days + 1 day off set by the company., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income tax (childcare, health insurance, training, etc.)., • Company benefits club, which allows 3P employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, Fnac, Rituals, El Corte Inglés, etc.)., • Flexible working hours during the week and a reduce work day on Friday of 7h., • Special Summer working day of 7h during July and August., • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • All new hires who reside outside of Navarra are provided with a relocation service and/or assistance. We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and cGMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human an animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. #J-18808-Ljbffr

¡Ampliamos nuestro equipo! 🔎 ¿Buscas un nuevo reto donde desarrollar tu carrera y aprender nuevas tecnologías? Entonces sigue leyendo porque esto te puede interesar. Scalian es una empresa de más de 6.000 personas con una dimensión internacional, con oficinas en Europa y América del Norte. Estamos especializados en dar servicios a diferentes clientes enfocados en Data, Cloud e Inteligencia Artificial. ¿Qué buscamos? Buscamos un/a profesional con experiencia en el sector industrial, para colaborar en la mejora del rendimiento y la capacidad productiva de un proveedor. La misión principal será ayudar a un supplier a alcanzar los niveles de producción planificados, trabajando de forma presencial en sus instalaciones y coordinando con el Tier 1 y el propio proveedor. Requisitos mínimos: • Experiencia de al menos 2 años en entornos industriales (Supply Chain y/o Calidad)., • Experiencia en "Transfers of Work" o trasferencias de trabajo, • Experiencia en sector aeroespacial será positivamente valorado, • Nivel alto de inglés hablado y escrito ¿Qué tendrás con nosotros? ⛱ 25 días laborables de vacaciones 💻 Teletrabajo 📝 Contrato indefinido 📚 Formación continua, certificaciones, meetups y planes de desarrollo profesional personalizados para que podamos seguir creciendo juntos. Contamos con acceso a plataformas internas con contenido abierto para que lo disfrutes cuando tú quieras y a tu ritmo. 🕐 Jornada completa con horario flexible para facilitar la conciliación entre vida familiar y profesional. 🎉 After works en las oficinas 🎂 La tarde del cumpleaños libre 🏋️ ♀️ Descuentos en gimnasios 💲Programas de retribución flexible: seguro médico, tarjeta restaurante, abono de transporte, cheques para escuelas infantiles. ⚖️ En Scalian valoramos la diversidad e impulsamos un entorno de trabajo inclusivo, donde todas las personas, independientemente de su género, identidad, edad o procedencia, puedan desarrollarse profesionalmente. 🌏 Como parte del grupo Scalian, abrimos nuestras fronteras y crecemos internacionalmente. ♻️ En el grupo apostamos por iniciativas sostenibles. ¡Despega en tu carrera con Scalian Spain!✈

Geek+ is a global technology company specializing in smart logistics. We apply advanced robotics and artificial intelligence technologies to create solutions for warehouse and factory operations. With the rise of e-commerce and the demand for faster and more flexible movement of goods, warehouse and manufacturing operators are facing increasingly complex production and logistic challenges today. Speed, product diversification, same-day delivery, volume, safety… these concerns are impacting a wide range of industries, from apparel, retail, automotive, to even electronics, energy and pharmaceutical industries. Geek+ was founded to be the solution to these problems. We make logistics affordable, efficient, flexible, safe and agile. Our vision is to establish a fully automated and intelligent supply chain globally. Responsibilities: • Participate in the full lifecycle of on-site implementation and project delivery for AMR-based warehouse automation projects across Europe, • Support the Project Manager in coordinating customers, suppliers, installation teams, and internal functions such as R&D, Product, and Software to ensure smooth project execution, • Track project schedules and coordinate and monitor on-site installation, equipment commissioning, system integration, testing, and acceptance activities, • Support the management of on-site work quality, safety, and operational compliance.Identify field issues and project risks in a timely manner and drive them toward effective resolution, • Prepare and maintain project documentation, including installation records, acceptance documents, risk lists, and lessons learned, • Support the coordination and management of on-site resources, including personnel, equipment, materials, and external partners, • Contribute to the standardization and continuous improvement of project delivery processes to improve implementation quality and delivery efficiency, • Travel frequently across Europe according to project requirements Required Qualifications, Capabilities, and Skills: • Bachelor’s or master’s degree in Industrial Engineering and Management, Electrical Engineering and Information Technology, Automation Engineering, or a related field, • Strong interest in project management, automation systems, and project delivery, • Good organizational, coordination, communication, and cross-functional collaboration skills, • Strong problem-analysis skills and the ability to proactively follow up on and drive issues toward resolution, • Responsible, proactive, and team-oriented, with a strong field service mindset, • Professional working proficiency in English. Spanish language skills are a plus, • Willingness and ability to travel frequently across Europe Preferred Qualifications: • Internship or professional experience in automation, logistics systems, equipment installation, or project implementation, • Experience in project coordination, supplier coordination, or customer communication, • A valid EU driving licence

3PBIOVIAN is seeking a QA Specialist (QC Laboratory) to join our Quality Assurance Team in Navarra. You will act as QA representative within the QC laboratory, ensure GMP compliance, and provide on-the-floor QA support across laboratory activities. The role requires at least 4 years in QA/QC in GMP environments, experience with data integrity, raw data review and deviation investigations, plus proficiency with LIMS, Empower 3 and Gen 5. A Bachelor’s in a related science is required. #J-18808-Ljbffr

¡Ampliamos nuestro equipo! 🔎 ¿Buscas un nuevo reto donde desarrollar tu carrera y aprender nuevas tecnologías? Entonces sigue leyendo porque esto te puede interesar. Scalian es una empresa de más de 6.000 personas con una dimensión internacional, con oficinas en Europa y América del Norte. Estamos especializados en dar servicios a diferentes clientes enfocados en Data, Cloud e Inteligencia Artificial. ¿Qué buscamos? Buscamos un/a profesional con experiencia en el sector industrial, para colaborar en la mejora del rendimiento y la capacidad productiva de un proveedor. La misión principal será ayudar a un supplier a alcanzar los niveles de producción planificados, trabajando de forma presencial en sus instalaciones y coordinando con el Tier 1 y el propio proveedor. Requisitos mínimos: • Experiencia de al menos 2 años en entornos industriales (Supply Chain y/o Calidad)., • Experiencia en "Transfers of Work" o trasferencias de trabajo, • Experiencia en sector aeroespacial será positivamente valorado, • Nivel alto de inglés hablado y escrito ¿Qué tendrás con nosotros? ⛱ 25 días laborables de vacaciones 💻 Teletrabajo 📝 Contrato indefinido 📚 Formación continua, certificaciones, meetups y planes de desarrollo profesional personalizados para que podamos seguir creciendo juntos. Contamos con acceso a plataformas internas con contenido abierto para que lo disfrutes cuando tú quieras y a tu ritmo. 🕐 Jornada completa con horario flexible para facilitar la conciliación entre vida familiar y profesional. 🎉 After works en las oficinas 🎂 La tarde del cumpleaños libre 🏋️ ♀️ Descuentos en gimnasios 💲Programas de retribución flexible: seguro médico, tarjeta restaurante, abono de transporte, cheques para escuelas infantiles. ⚖️ En Scalian valoramos la diversidad e impulsamos un entorno de trabajo inclusivo, donde todas las personas, independientemente de su género, identidad, edad o procedencia, puedan desarrollarse profesionalmente. 🌏 Como parte del grupo Scalian, abrimos nuestras fronteras y crecemos internacionalmente. ♻️ En el grupo apostamos por iniciativas sostenibles. ¡Despega en tu carrera con Scalian Spain!✈

We are your Energy Technology Partner . We electrify, automate, and digitalize every industry, business, and home, driving efficiency and sustainability for all. La siguiente información ofrece un resumen de las habilidades, cualidades y cualificaciones necesarias para este puesto. At Schneider Electric, our values – IMPACT (Inclusion, Mastery, Purpose, Action, Curiosity, Teamwork) – are the foundation of everything we do. Becoming an Impact Maker means turning sustainability ambitions into actions at the intersection of automation, electrification, and digitization. Are you ready to lead the digital transformation to create a more sustainable world? If you are up to challenge your creativity and make an impact, we are excited to welcome you! As a Senior Project Manager , you lead the end-to-end execution of projects involving physical products, electromechanical hardware, equipment and infrastructure , ensuring delivery within committed timelines, budget, quality and customer requirements, aligning team efforts with offer goals and ensuring that Agile principles and practices are adhered to throughout the offer lifecycle. You coordinate cross-functional engineering teams and work closely with stakeholders involved in areas such as electromechanical, testing, marketing, industrialization, manufacturing and supply chain . This role requires a strong Project Management background in electronicmechanical hardware or industrial environments . Experience with Agile and Scrum methodologies is also important, as you will work with backlogs, priorities, iterations and cross-functional teams. However, this is not a software-focused Scrum Master position : the core of the role is managing the execution of projects linked to tangible products and systems. You ensure alignment and partnership with Product Owners and other stakeholders to ensure portfolio prioritization and execution throughout the project lifecycle. You translate objectives and customer requirements into clear execution plans, coordinate activities across different disciplines, and manage risks, dependencies, resources, costs and timelines. You facilitate the appropriate Agile/Scrum rituals, support backlog prioritization and help teams improve their way of working. You remove impediments, drive decision-making and promote continuous improvement while keeping a strong focus on delivery and project execution . You exercise independent judgment to resolve issues impacting project results, often working across multiple teams and in situations where priorities or dependencies may change. You act as an intermediary between the development teams and stakeholders, ensuring that all parties are kept informed and aligned. Key Responsibilities Lead the end-to-end execution of projects related with electromechanical hardware products , from customer requirements through planning and delivery. Enable aligned execution with Team/Squad goals and backlog. Deliver the global roadmap of offers and releases, considering technology, feasibility, resources, and faster Time-to-Market Develop. Coordinate cross-functional teams and ensure clear ownership of activities and deliverables, Product Portfolio Management management, including the milestone planning, budget forecasting, and tracking on the expense and resource. Partner with the Product Owner and key stakeholders to align priorities, backlog and project execution. Apply Agile/Scrum where appropriate to organize and improve project delivery. Facilitate key team rituals such as planning, regular team updates, reviews and retrospectives. Identify and manage project risks, dependencies and impediments , driving decisions and escalation when needed. Coordinate with suppliers, factories, external partners or customers when required by the project. Communicate, provide clear project status to stakeholders and act as a key point of contact for project execution. Support continuous improvement and help execution teams improve performance, collaboration and autonomy. Qualifications Must have Significant experience as a Project Manager, Technical Project Manager or similar role managing engineering projects . Proven experience managing projects involving electromechanical hardware, physical products, industrial equipment or electromechanical systems . Experience coordinating cross-functional teams . Strong experience managing project scope, milestones, risks, dependencies, resources, budgets and timelines. Experience working with Agile, Scrum . Strong stakeholder management, communication, facilitation and decision-making skills. Comfortable working in technical environments with multiple disciplines and dependencies. Strong demonstrable leadership skills. Nice to have Experience with product development, prototypes, testing, validation, industrialization, manufacturing, marketing in complex environment. Scrum Master, Agile or Project Management certification. Experience using Jira and project portfolio management tools . Experience working with Product Owners and managing backlogs. Experience with Offer Change Management and Offer Life Cycle Management milestones. Experience coordinating suppliers, factories or external partners. We adapt to you: With our flexible schedule, you'll have the freedom to adjust your work hours to accommodate your personal needs and responsibilities. We know how great it is to work from home. With our hybrid work plan, you can enjoy working from the comfort of your home. Need more time to relax and disconnect? With our Holy Pack, you can purchase additional vacation days to recharge when you need it most. Celebrate holidays your way! With Floating Holidays, you can exchange holidays for other days that better suit your plans and personal preferences. Need additional time to explore new experiences or focus on personal projects? With the Sabbatical Pack, you can request up to 2 months of extra leave (unpaid). We value the importance of family and want to support you in all aspects of your life. Our Global Family Leave Policy provides flexible paid conditions for when you need it most, whether you're about to be a parent, need time to overcome a loss, or to care for a loved one. We take care of you: With access to the health and wellness platform Wellwo, you and up to 5 people of your choice can enjoy access to wellness content, nutrition counseling, fitness classes, and more! From dance classes to booking a hotel spa, we offer an agreement with Wellhub so you can access a network of thousands of gyms and sports centers to keep your body active in the way you like best. Your well-being is our priority. You will have medical service at your workplace for close attention to any medical needs. We empower you: With Career Hub, our AI-driven professional development platform, you can connect with job opportunities, projects, and mentors at Schneider Electric globally. We offer you the opportunity to be a shareholder of Schneider Electric and share in our achievements with our stock ownership program. We celebrate everyone's talent and success with our recognition program, through which you can give and receive points for your achievements and redeem them for gift cards at your favorite stores. You will have life insurance for your protection. We offer you a Flexible Remuneration Plan in which you can choose from a variety of options, such as health insurance, meal vouchers, childcare vouchers, transportation vouchers, training, and more. With Club Schneider, you will enjoy special discounts at your favorite stores, restaurants, travel agencies, and other external services. xiphteb Participate in company-subsidized volunteer programs to contribute to our community and have a positive impact on your environment. Bring your Agile expertise to a team that's ready to achieve great things together — apply now!

LLM Language Evaluation Specialist – Spain Project-based | Spain | Remote We are looking for Catalan language specialists to participate in a long-term LLM Language Evaluation Project focused on evaluating the quality and accuracy of AI-generated content. The project is expected to continue for 3+ months, with selected candidates first completing a trial evaluation before joining the production stage. 🔍 What You Will Do • Evaluate AI/LLM-generated content in Catalan according to detailed project guidelines., • Assess whether the content is accurate, natural, and linguistically appropriate., • Identify and classify language-related issues, including:, • Mistranslation or inaccurate translation, • Missing or omitted content, • Incorrect terminology or word usage, • Spelling, grammar, punctuation, and spacing errors, • Word- or phrase-level issues, • Other issues affecting the quality and readability of the content, • Identify abnormal cases, such as non-Slovak content, language identification errors, duplicate content, or content requiring rejection., • Apply evaluation criteria consistently and provide structured evaluation results., • Maintain high accuracy and attention to detail throughout the project. 🎯 Requirements • High proficiency in Catalan., • Previous experience with Large Language Model (LLM), AI evaluation, AI training, data annotation, localization, translation, or related projects is required., • Strong understanding of Slovak grammar, vocabulary, terminology, and natural language usage., • Strong ability to identify subtle language errors and distinguish between acceptable and incorrect expressions., • Ability to understand and follow detailed evaluation guidelines., • Strong attention to detail and execution ability., • Comfortable working with structured digital documents and online tools. Relevant professional or industry experience is a plus, but not mandatory. 📋 Project Information • Project: LLM Language Evaluation, • Target Language: Catalan, • Duration: 3+ months, • Work Mode: Remote / Project-based, • Start: September 24, 2026. Before starting project work, all selected candidates will go through a 1–5 day trial and training period to familiarize themselves with the project guidelines and evaluation process. The trial and training period is paid at the normal project rate, so candidates will be compensated for their time and completed work during this period. Recruitment Notice We never charge candidates any fees at any stage of the recruitment or onboarding process.

Reconnect customers. Build relationships. Create new opportunities. At andagon, we have been focused on software quality for more than 25 years. We support companies with Quality Assurance, Software Testing and Test Automation – and we want to further strengthen and develop our existing and former customer relationships. We are looking for a Customer Success & Reactivation Manager who enjoys connecting with people, building relationships and turning great conversations into new business opportunities. Your Responsibilities • Reactivate former and inactive customers and bring existing relationships back to life, • Build and develop long-term relationships with key contacts and decision-makers, • Understand customers’ current challenges, needs and upcoming projects, • Identify up-selling and cross-selling potential and develop qualified business opportunities, • Ensure consistent follow-up and manage customer activities in our CRM, • Work closely with Sales and Delivery to turn customer needs into concrete solutions and projects What You Bring • Experience in Customer Success, Account Management, Inside Sales or Business Development in a B2B environment, • Experience in proactive customer outreach and developing existing or former customer accounts, • Strong phone communication skills and confidence in proactively approaching customers – you don’t wait for customers to come to you, • Commercial mindset and the ability to identify customer needs and business potential, • Strong communication skills, reliability and consistent follow-up, • Structured, independent and results-oriented way of working, including confident use of CRM systems, • German C1–C2 and English B2 or higher A plus: Experience in IT services, IT consulting, SaaS or Software Quality, as well as up-selling and cross-selling. What You Can Expect A role with a high level of ownership and direct impact on our customer development. You will take over existing contacts and former customer relationships with real potential – and have the freedom to turn them into new conversations, opportunities and long-term partnerships. If you enjoy combining relationship management with a commercial mindset and are motivated by reconnecting and developing customers, we’d love to hear from you.

• Role: Video Creator (Remote), • Location: Remote (Work from Anywhere) Role Overview: We are hiring for one of our clients, seeking a Video Content Creator (US based) to work on a full-time basis. The role involves producing short, dynamic “walk-and-talk” videos that showcase interesting locations near you. You’ll help capture authentic, human perspectives that reflect the character, diversity, and beauty of your surroundings. Key Responsibilities: • Create 1–5 minute “walk-and-talk” videos highlighting public places in your city such as parks, landmarks, markets, or cultural spots., • Speak naturally on camera, providing friendly, conversational commentary as if guiding a viewer in person., • Record smooth, steady footage using your smartphone or camera with clear audio., • Choose safe, public locations where filming is legally allowed and follow provided creative guidelines., • Submit videos along with accurate location details such as name and address or coordinates. Required Skills & Qualifications: • Comfortable speaking on camera in English with clear communication., • Creative, personable, and confident presence on video., • Owns a smartphone or recording device with good video and audio quality., • Reliable internet connection for uploading videos., • Ability to follow task guidelines and deliver videos on schedule. More About the Opportunity: This role offers a unique opportunity to work with a global leader in the technology industry, contributing to the training of AI systems to better understand and describe the world. The position supports a cutting-edge initiative designed to enhance natural, engaging human perspectives in AI training data. Equal Opportunity Employer: We hire based on skills and expertise. All qualified candidates are welcome regardless of background, experience, or prior employment history. Applications are reviewed solely on demonstrated technical ability and qualifications. Apply Now!

Clinical Study Lead, Precision Medicine 2 positions | New role within MDx CRO's Precision Medicine team About the role MDx CRO is creating two new Clinical Study Lead positions within our Precision Medicine Clinical Alliances team. This is not a conventional CRA role. It is not a purely regulatory role either. It sits where biomarker science, investigational IVDs, clinical operations and drug development meet. You will lead the IVD and biomarker study workstream within complex drug development programmes, translating regulatory strategy into country activation, testing site and clinical site execution, and high-quality study delivery. You will need to move confidently between Competent Authorities, Ethics Committees, pharmaceutical sponsors, diagnostic partners, CRO teams, testing laboratories and clinical sites. You will understand not only how to obtain study approval, but also how the diagnostic component must operate inside a clinical trial so that the resulting evidence remains robust and usable. The role is international, client-facing and hands-on. International travel may be required for testing-site activities, monitoring, clinical sites, client meetings and other study activities. What you will own • Lead the IVD performance-study workstream within combined clinical trials and other biomarker-driven drug development programmes., • Lead submission strategy and execution to National Competent Authorities and Ethics Committees, including initial applications or notifications, country adaptations, requests for information, amendments, substantial modifications and ongoing authority or committee correspondence., • Coordinate the preparation and review of country submission packages, including CPSPs, relevant protocol content, informed consent language, site suitability documentation, national forms and other study-specific materials., • Drive country start-up and activation readiness, ensuring applicable regulatory and Ethics Committee conditions are understood, tracked and resolved., • Plan and conduct IVD study monitoring and testing-site or laboratory oversight in line with GCP, IVDR, ISO 20916, applicable study documents and MDx quality procedures., • Review execution where diagnostic evidence is actually generated, including sample and testing workflows, protocol compliance, traceability, study documentation, deviations, data quality and corrective actions as applicable., • Identify and escalate issues that could affect study integrity, diagnostic evidence, country activation, downstream regulatory strategy or the therapeutic development programme., • Coordinate across pharmaceutical sponsors, diagnostic manufacturers, CRO and clinical-trial teams, central or local laboratories, clinical sites, local representatives and country specialists., • Maintain clear multi-country trackers, submission records, timelines, study files, decisions and client communications., • Apply knowledge of global regulatory frameworks for biomarker-based drug development, including the EU IVDR and clinical-trial interface, FDA investigational IVD, IDE and companion-diagnostic considerations, and country-specific authority and ethics requirements., • Contribute to client meetings, regulatory intelligence and the continued development of MDx country knowledge and Precision Medicine delivery methods. Who we are looking for You should bring a degree in life sciences, biomedical sciences, molecular biology, pharmacy, clinical research or a related discipline, together with demonstrable hands-on experience in clinical or performance-study delivery. We are particularly interested in candidates who combine NCA and Ethics Committee/IRB submission experience with clinical monitoring or study-management experience. You should be comfortable working with IVDs, molecular diagnostics, clinical-trial assays, biomarkers or companion diagnostics, and understand how diagnostic testing can influence patient selection and therapeutic development. Working knowledge of GCP is expected. Experience with IVDR performance studies and ISO 20916 would be particularly valuable. Experience in any of the following would strengthen your application: combined therapeutic and diagnostic programmes, CDx development, CTIS and the EU clinical-trial environment, FDA investigational IVD or IDE frameworks, NGS or molecular pathology, central laboratory networks, multi-country submissions, and management of regulatory or Ethics Committee RFIs. You will also need excellent written and spoken English, strong project-management and organisational skills, sound judgement, and the confidence to communicate directly with international clients and study stakeholders. Most importantly, you need to be comfortable taking ownership of complex problems where the regulatory, clinical and diagnostic answers are interconnected. What success looks like You make complex studies feel controlled. Submission packages are coherent and country-ready. Authority and Ethics Committee questions are anticipated and answered well. Sites and testing laboratories understand what is expected. Monitoring identifies issues before they become critical. Pharmaceutical and diagnostic stakeholders remain aligned. Most importantly, the programme generates evidence that remains useful for both the therapeutic and diagnostic development objectives. Why MDx CRO You will join a Precision Medicine organisation deliberately designed to combine client-facing clinical leadership with deep scientific and technical capability across diagnostics, IVD regulation, NGS, bioinformatics, statistics and software. You will have direct client exposure, meaningful study ownership and the opportunity to work on complex international programmes where clinical, regulatory and diagnostic decisions genuinely intersect. Because this is a new position, you will also help shape how the Clinical Study Lead role develops as our Precision Medicine organisation grows. Apply Apply through LinkedIn. • If you understand both the clinical trial and the diagnostic behind the biomarker, we would like to hear from you.

Principal Biostatistician | Global CRO | Home Based | Spain | Permanent | We are partnering with a leading global CRO to recruit an experienced Principal Biostatistician to join their growing biometrics team. This is an excellent opportunity for a Principal Biostatistician looking to take on a highly visible role, providing statistical leadership across complex global clinical trials while working closely with pharma and biotech clients. You will lead studies and regulatory submissions, collaborate with cross-functional teams and external stakeholders, mentor junior statisticians, and play a key role in delivering high-quality clinical development programmes. This is a fully home-based position (Poland, Spain, Romania, Bulgaria, Czech Republic or Hungary). What you will be doing: • Lead biostatistics activities across individual studies, programmes of studies and regulatory submissions, • Provide statistical leadership and oversight throughout the clinical development lifecycle, • Review and approve study protocols, Statistical Analysis Plans (SAPs), clinical study reports and other key statistical deliverables, • Collaborate with sponsors, project teams and regulatory agencies to ensure high-quality study delivery, • Provide statistical consultancy to support proposal development, project planning and budgeting, • Participate in bid defence meetings and client presentations, representing the biostatistics function, • Mentor and support junior statisticians while promoting best practices across projects, • Ensure all statistical deliverables are produced to the highest quality and in accordance with regulatory requirements What you will need: • MSc or PhD in Biostatistics, Statistics or a related discipline, • 7+ years' experience (PhD) or 9+ years' experience (MSc) within clinical biostatistics, • Extensive experience supporting Phase I-IV clinical trials within a pharma or CRO environment, • Strong knowledge of statistical methodologies, clinical trial design and the drug development process, • Experience leading multiple studies, submissions or clinical programmes, • Excellent communication and stakeholder management skills with proven leadership experience, • Ability to work effectively across cross-functional and international project teams What's in it for you: • Competitive salary and comprehensive benefits package including medical, dental, vision, pension and life insurance, • Fully home-based in Poland, Spain, Romania, Bulgaria, Czech Republic or Hungary, • Excellent long-term career development and progression opportunities, • Structured learning and development programmes, • Opportunity to work on innovative global clinical development programmes within a collaborative and supportive environment What to do next: If this opportunity is of interest, please apply now with your CV as the organisation is looking to welcome an experienced Principal Biostatistician to the team as soon as possible. Not what you're looking for? Please contact Jo Fornaciari at for a confidential discussion about potential other opportunities in the UK and across Europe.