Trabajos Salud y Servicios Sociales en Cerdanyola Del VallèsCrear alertasJornada completa

Seeking a senior full-stack engineer to develop and implement features, taking ownership of product areas and driving projects from research to delivery.

Seeking a Gerocultor/Caregiver with experience in elder care for a long-term full-time position at a nursing home. Responsibilities include assisting residents with daily needs and participating in activities.

Seeking a certified caregiver for temporary coverage. Responsibilities include elder care. Must have official certification and experience in the elderly sector. Knowledge of ACP and Catalan language required.

Seeking Dentists (General Practitioners, Orthodontists, Prosthodontists) to relocate to private practices in Ireland. Requires a Bachelor in Dental Surgery and advanced English.

Lead a team of developers in the design, development, and delivery of new features and enhancements for the Secure GPT service, ensuring the timely delivery of high-quality features that meet acceptance criteria and align with the product vision. Define and prioritize user stories based on business value and user needs, and manage the product backlog to reflect the latest priorities and business objectives. Develop new functions and enhancements around Secure GPT API usage while identifying opportunities for improvement in API Operations processes, particularly in observability automation and customer service delivery. Take ownership of service issues and incidents, troubleshooting and resolving API-related issues to ensure seamless user experience and high service availability, and serving as a point of escalation for stakeholders seeking assistance. Ensure compliance with security, regulatory requirements, and data privacy standards related to the Secure GPT service. Communicate effectively with stakeholders to gather feedback, provide updates, and align on product direction, collaborating with the broader Secure GPT international team to deliver exceptional customer service to internal stakeholders. About The Job Main missions Your Responsibilities Include Lead a team of developers in the design, development, and delivery of new features and enhancements for the Secure GPT service, ensuring the timely delivery of high-quality features that meet acceptance criteria and align with the product vision. Define and prioritize user stories based on business value and user needs, and manage the product backlog to reflect the latest priorities and business objectives. Develop new functions and enhancements around Secure GPT API usage while identifying opportunities for improvement in API Operations processes, particularly in observability automation and customer service delivery. Take ownership of service issues and incidents, troubleshooting and resolving API-related issues to ensure seamless user experience and high service availability, and serving as a point of escalation for stakeholders seeking assistance. Ensure compliance with security, regulatory requirements, and data privacy standards related to the Secure GPT service. Communicate effectively with stakeholders to gather feedback, provide updates, and align on product direction, collaborating with the broader Secure GPT international team to deliver exceptional customer service to internal stakeholders. Expected Skills & Experience Experience Bachelor's or Master's degree in Computer Science, Software Engineering, or a related field 7+ years of experience as a software engineer, with at least 3-5 years in a lead or senior role Proven track record of successfully leading the delivery of complex software projects Experience in managing and mentoring a team of software engineers Technical Skills JavaScript/TypeScript development (Node.Js) for the backend Github / DevOps experience Experience in API operations and management Competence in monitoring resources on Azure Knowledge of Infrastructure as Code (IaC) Terraform and/or Bicep for automatic infra deployment Expertise in software design patterns, architecture principles, and development methodologies Familiarity with agile software development practices and tools (e.G., Scrum, Kanban, Git, CI/CD) Experience with cloud-based technologies and platforms (e.G., AWS, Azure, GCP) Strong understanding of software testing, debugging, and performance optimization techniques Soft Skills English : Independent user (C1) Ability to travel / ability to be relocated for short periods in other countries (France/Spain/Portugal) Leadership: Ability to inspire and motivate a team, provide guidance, and make decisions Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams Strong problem-solving and critical thinking abilities, with a focus on delivering innovative solutions Ability to prioritize tasks, manage multiple projects, and adapt to changing business requirements Demonstrated leadership skills, with the ability to motivate and inspire a team Commitment to continuous learning and professional development What We Offer We bring together the expertise, cultural diversity and creativity of over 8,000 employees worldwide and we’re committed to equal opportunities in all aspects of employment (gender, LGBT+, disabled persons, or people of different origins) and to promoting Diversity & Inclusion by creating a work environment where all employees are treated with dignity and respect, and where individual differences are valued. About The Entity AXA is becoming a sustainable tech-led company and at AXA Group Operations we are one of the major catalysts for this transformation. We set the tone by triggering and empowering the evolution of our insurance business model through technology and innovation, driving its concrete implementation globally at speed, with a high quality of advisory and execution. We are present across 17 countries with committed, highly qualified teams. We leverage technology, data, sourcing, security and investment allocation in a global way, but also achieve economies of scale and synergies when necessary. At AXA Group Operations, we want to be recognized in three fields of action: State-of-the-art Data Technology to drive customer experience State-of-the-art Procurement & Sourcing to drive efficiency and better manage risks High-Performing Global Team for stronger partnerships with AXA entities About AXA As a world-leading insurance company, we act for human progress by protecting what matters. With 153,000 employees in 54 countries working for 105 million customers, we’ve created a truly dynamic and vibrant community. Inclusion and diversity link closely with our values, and together we’re nurturing a culture of respect, for each other, for our customers and the communities around us. Join AXA and you’ll feel like you belong, are included and can thrive. You’ll be able to shape the way you work and truly grow your potential as you seek out new opportunities, push boundaries and benefit people in critical moments of their lives. This is your chance to build the tomorrow you want. Know you can. #J-18808-Ljbffr

Computational Scientist - Deep Tech Newton Colmore is proud to be working with a venture that sits at the intersection of AI, biology, and advanced process engineering.We are assisting them in their search for a computational scientist to play a foundational role in the development of their data-rich product. This is a rare opportunity to join a highly ambitious, venture-backed team transforming complex industrial processes into intelligent, predictable, and controllable systems.The successful candidate will help build the modelling and machine learning capabilities that underpin a platform that aims to transform how process data is viewed and utilised. The position offers significant autonomy, technical ownership, and a clear path for growth. As a computational scientist, you will own the development of advanced computational models spanning mechanistic process understanding, machine learning, digital twin technology, and real-time predictive intelligence. Working closely with a multidisciplinary team of scientists and engineers, you will apply cutting-edge mathematics, modelling, and AI techniques to solve complex industrial challenges with real-world impact. The role will also provide an opportunity to build novel predictive models using advanced sensor technology, then looping the data back to the engineering and science teams to ensure that constant iterations and alterations can be made. We are looking for candidates with strong mathematics fundamentals, ideally applying them within a highly complex scientific and engineering field.This will be complemented by experience with working on digital twin technology, simulation platform sand predictive process models. Any additional experience with industrial monitoring applications and/or chemical manufacturing would be highly advantageous. In their pursuit of hiring outstanding engineers and scientists, the company are offering a competitive package with share options and the potential to help with relocation (case by case basis).This mixed with direct access to the founders, and investors, it could be a great destination for the next part of your career, working on something that is aiming to be truly transformational. #J-18808-Ljbffr

Mobile unit officer for teleassistance service, providing direct care, emergency response, and administrative support to users in their homes. Requires a driving license, basic training/experience, and high Catalan proficiency.

Time Out Group in Barcelona seeks a Senior Programmatic & Ad Tech Specialist to optimize our global ad tech stack (GAM, Prebid) and maximize SSP revenue across markets. This hybrid role blends audience monetization, partner management, and privacy compliance. You will own SSP and demand-partner relationships, monitor eCPMs, manage first-party data strategies, and troubleshoot programmatic delivery with DevTools. Fluent English required; based in Spain with 1 day per week in the Barcelona office. #J-18808-Ljbffr

Location: Barcelona and surrounding areaWorking model: Hybrid - 4 days remote, 1 day per week in our Barcelona officeOffice: KPS Iberia, C/ Pau Claris 162-164, 08037 Barcelona About KPS KPS is a global consulting and technology company delivering digital transformation and e-commerce solutions for leading international clients. At KPS Iberia, you will work in an international and agile environment on complex digital platforms and business-critical technology solutions. We are looking for an experienced Senior Tech Lead / Full-Stack & DevOps Engineer to join KPS Iberia and work on complex, end-to-end digital and e-commerce platforms for major international clients. This is a hands‑on technical leadership role. We are looking for someone who combines strong software engineering expertise with proven experience leading and coordinating developers, driving technical execution and ensuring successful delivery. The role combines architecture, technical project leadership and hands‑on engineering. You will work closely with developers, guide technical decisions, and actively contribute to the implementation of technical solutions. Your Responsibilities Understand, analyse and evaluate existing software/system architectures. Proactively identify and propose technical improvements and necessary adaptations. Make architecture decisions and help shape scalable and sustainable technical solutions. Provide hands‑on support in the implementation of technical solutions. Take responsibility for technical project leadership. Coordinate developers and ensure effective collaboration within the team. Support the team in resolving technical challenges and maintaining high engineering quality. Communicate technical concepts and decisions clearly to both technical and non-technical stakeholders. Your Profile Several years of experience as an Architect, Senior Architect, Tech Lead or in a comparable technical leadership role. Very strong frontend expertise, particularly with JavaScript, Node.Js and React. Experience in backend development, ideally with Java. Ability to understand, assess and further develop software/system architectures. Solid experience with Cloud Systems (AWS, Azure and/or GCP). A strong hands‑on mentality and willingness to actively contribute to technical solutions. Good understanding of DevOps practices and modern software delivery processes (Docker, Kubernetes, Terraform, CloudFormation, Pulumi or similar, CI/CD pipelining etc.). Experience coordinating developers and leading technical workstreams ideally in an international environment. Strong communication skills in English, as our projects are international and conducted in English. Nice to have Knowledge of container technologies and modern deployment processes. Experience in complex e-commerce, SaaS or digital platform environments. Experience with AI-assisted development, agentic coding or modern AI engineering tools. Good knowledge of security best practices, IAM, secrets management and OWASP principles. What We Offer Architectural responsibility in complex digital and e-commerce projects. The opportunity to shape technical solutions for major international clients. A role combining architecture, technical leadership and hands‑on engineering. An international and collaborative working environment. Modern technologies and agile ways of working. The opportunity to work closely with experienced developers, architects and business stakeholders. Clear opportunities to further develop your architecture and technical leadership career. A hybrid working model with four remote days and one day per week at our Barcelona office. Employment under a Spanish employment contract. #J-18808-Ljbffr

Seeking a qualified EU-trained dentist for a full-time position in a modern Dutch dental clinic. Offers relocation assistance, language training, and a salary of €4500-€6500 monthly.

ODONTOLOGIA GENERALCLINICA DENTAL SANT LLUISBarcelona, BarcelonaDentista / OdontólogoJornadaJornada completa## DescripciónOferta de Empleo: Odontólogo/a GeneralUbicación: Clínica DentalTipo de contrato: Jornada completaIncorporación: InmediataDescripción del puestoBuscamos un/a Odontólogo/a

Seeking a Laboratory Technician for High Throughput Experimentation Unit to support research in chemistry, focusing on rapid exploration of chemical reaction space via parallel execution and analysis of microscale reactions.

"Delivering innovative digital magazine content on every device in every country" We are seeking a Senior Dev Ops Engineer to join our Barcelona office. ZINIO powers some of the largest digital content distributors in the market. Newsstands, retailers, media service providers, inflight entertainment and libraries offering incremental revenue, auditable paid circulation, and valuable brand exposure for publishers worldwide. ZINIO solves the logistical challenges of a complex digital ecosystem and unlocks new revenue and subscription opportunities for publishers from managed apps & newsstands through to fulfillment services, APIs & content readers. About the Role: The Senior Dev Ops Engineer will design, operate, secure, and improve our infrastructure and production systems. The role combines Dev Ops, Site Reliability Engineering, and infrastructure security, with a focus on automation, observability, scalability, reliability, and secure operations. Working closely with development and infrastructure teams, you will automate processes, improve deployment and recovery, investigate technical issues, and contribute to reliable and secure systems. What you will do: Manage and improve infrastructure across cloud and internal environments. Design and maintain production systems that meet defined availability, scalability, and reliability requirements. Automate infrastructure provisioning, configuration, deployments, and operational processes. Manage servers, applications, containers, networking, and infrastructure services. Develop and maintain Infrastructure as Code and configuration management practices. Develop and maintain CI/CD pipelines and deployment processes. Define and maintain deployment, rollback, disaster recovery, and business continuity procedures. Implement monitoring, logging, alerting, and observability practices. Define and monitor SLOs, SLIs, and system performance metrics. Investigate production incidents, identify root causes, and implement corrective actions. Conduct capacity planning, scalability testing, and performance analysis. Work with development teams to improve application reliability, performance, and operational readiness. Identify and address infrastructure and application security risks. Implement security controls across infrastructure, cloud services, networks, applications, and deployment pipelines. Manage access controls, secrets, credentials, certificates, and other security mechanisms. Support vulnerability management, security hardening, patching, and security incident response. Maintain technical documentation, operational procedures, and runbooks. Contribute to improvements in infrastructure architecture, reliability, security, and operational processes. What you will bring: Experience in Dev Ops, Site Reliability Engineering, Systems Engineering, Infrastructure Engineering, or a related technical field. Experience administering and troubleshooting Linux-based systems. Knowledge of networking, HTTP, DNS, TLS/SSL, load balancing, and common infrastructure components. Experience with cloud platforms, including AWS or equivalent. Experience designing, implementing, or operating production systems with defined availability and scalability requirements. Experience automating technical and operational processes using Python, Go, Type Script, Bash, or another suitable programming language. Experience with Infrastructure as Code and configuration management tools such as Terraform, Open Tofu, and/or Ansible. Experience with Docker and containerized environments. Experience with CI/CD pipelines and automated deployment processes. Experience with monitoring, logging, alerting, and observability platforms. Experience investigating production incidents, including troubleshooting and root cause analysis. Knowledge of infrastructure and cloud security principles, including authentication, authorization, secrets management, and network security. Experience with vulnerability management, security hardening, WAFs, firewalls, or access controls. Experience with web servers and reverse proxies such as Varnish, Nginx, or Apache. Knowledge of load balancing, caching, CDNs, and distributed systems. Ability to communicate technical information clearly and maintain technical documentation. Ability to investigate technical problems, evaluate solutions, and implement appropriate changes. Experience with AWS security services, SIEM/security monitoring, or security automation is an additional qualification. What we offer: Competitive Compensation: Enjoy a competitive salary package, with annual salary reviews based on performance. Collaborative Environment: Work alongside a highly skilled, multicultural team. Dynamic Growth: Play a key role in driving the future of a fast-evolving company in the tech and content delivery space. Work Flexibility: Enjoy flexible working hours with a hybrid model, balancing in-office and remote work. Comprehensive Benefits: Attractive benefits package, including health insurance, meal cards, and transportation perks. Continuous Development: Access ongoing learning and professional growth opportunities. Remote work from abroad (up to 1 month per year), depending on destination and policy. Office Perks: Fresh fruit, tea, coffee, and a vibrant office environment. We are an equal opportunity employer committed to building a diverse and inclusive workplace. We welcome applications from people of all backgrounds and are committed to a fair recruitment process where employment decisions are based on skills, experience, qualifications, and the requirements of the role. #J-18808-Ljbffr

ALDIA, a multinational technology and engineering consultancy, is seeking a Software Control DSP Engineer to join its Spain team. The role focuses on DSP control algorithms and TI platform integration to deliver robust automotive, industrial, or telecom solutions. The ideal candidate has hands-on experience with DSP development, TI DSP components, and a practical approach to software in embedded environments while collaborating with multinational consultants. #J-18808-Ljbffr

In Materialise’s Staff department, we believe that meaningful impact starts with people and their expertise. If you’re passionate about shaping a strong, effective, and forward-looking organization, you’ll love being a part of this team. Through the knowledge and dedication of these teams, we’re creating value every day and building the foundation for long-term success. We are looking for a Functional Analyst for the Microsoft Dynamics 365 Finance and Operations platform to help transform the company's financial and operational processes using modern technologies. You will join a cross-functional team working on the implementation and optimization of business solutions in the field of finance, logistics, and resource management. If you have experience working with D365 F&O and strive to influence strategic processes, this role is for you. What You Will Do Gather information from and collaborate with different types of stakeholders (finance, procurement, warehouse, IT) Understand strategic business needs and plans for growth Gather and document detailed business requirements and transform them into user stories, including acceptance criteria Create, document, and maintain solution designs Execute standard and advanced configuration of the system, giving demos/prototypes to business users Prepare functional gap design documents Test new configurations and customizations — ensuring the provided functionality is in line with existing flows and satisfies stakeholders' needs and requirements Organize key user validation process, support for end-to-end user acceptance testing Users' consultancy and support; handle tickets asa second-level support engineer Follow the Change and Release management process Prepare release notes Manage tasks (AzureDevOps/Jira) Your profile Upper-intermediate English 3 years' experience with Microsoft Dynamics 365 Finance&Operations implementation and support Extensive experience in Microsoft Dynamics 365 Finance&Operations implementation projects Strong knowledge of standard D365 functionalities and most of the business processes listed below: Accounting policy (General Ledger, account structure, period close, etc.) Accounts payable Accounts receivable Manufacturing accounting Inventory accounting (closing and adjustment, inventory revaluation, inventory counting, inventory posting etc.) Cost accounting Tax accounting (understanding of business process flows) Subscription billing (nice to have) Electronic reporting Experience in supply chain management flows is a plus Experience working in an integrated environment (and understanding of the approach of working with it) Experience with AzureDevops/Jira UML/BPMN knowledge is a plus Experience in preparing user stories, user manuals, and release notes Able to adapt requirements to both technical and business languages Experience with the preparation of different types of products and project documentation Experience with organizing validation activities (user acceptance testing) A technical background is an advantage Logical and analytical thinking Independent research on solutions A critical thinker, detail-oriented, and self-organized What’s Waiting For You Work that matters The technology we build at Materialise pushes the boundaries. You’ll find pride in building something that matters, whether you designed it, printed it, or shipped it. No matter your role, we unlock new possibilities to build a better and healthier world every day. At Materialise, we expect you to think about the customer, not just the task. You push for better solutions and care about the difference your work makes. A people-centered space When you join Materialise, you join a group of colleagues invested in you, not just your work. From your own team to a department across the world, you’ll find a sense of belonging with people who help without being asked, challenge you, and have your back. At the same time, we expect you to invest in the people around you — not just your own work — to make the group stronger than the sum of its parts. An environment of trust As a company of innovators, we know how crucial autonomy is in your work. When we hire you, we trust in your expertise, giving you space to organize your tasks, work flexibly, and make your own calls. At Materialise, we expect you to deliver on that trust and keep your commitments. A career ready to build When you see opportunities for your career to grow at Materialise, we encourage you to go for them. People shape a fulfilling career at their own pace here. At Materialise, we expect you to take initiative in your own development. Don’t wait for someone else to plan your career. Step into the space and make it count. Make a difference in our Staff department. #J-18808-Ljbffr

Is this you?Titan Operating System S.L. (Titan OS), the Barcelona-based technology, entertainment, and advertising company is looking for you!Our platform combines content discovery and advertising technology in one solution, helping leading TV brands unlock greater value. Titan OS powers devices from major brands including Philips, AOC and JVC, reaching millions of viewers across Europe and LATAM. Titan OS is also powering free premium FAST Channels on selected SONY Android TVs.Over the last two years, Titan OS has grown revenue 10x and attracted leading investors, including Highland Europe and Mangrove.At TitanOS, we live by three core values:Make things happen – We take ownership, move fast, and deliver impact.No ego – We collaborate with respect and humility to reach shared goals.Show genuine passion – We love what we do and never stop learning.Culture and environment are at the heart of our ethos. If the above resonates with you, keep reading because we believe you could be a perfect addition to our incredible team!Role overview:We are looking for an entrepreneurial and performance-driven DSP Partnership Director to lead the implementation, optimization, and measurement of performance campaigns across CTV in the European market.The ideal candidate combines strong technical expertise in CTV advertising and DSPs with a deep understanding of performance marketing, data-driven audience targeting, and campaign optimization. This person will play a key role in ensuring campaigns meet their performance objectives, translating insights into actionable improvements, and driving continuous growth.Key responsibilities:Lead and manage the end-to-end implementation of performance campaigns on CTV, leveraging relevant DSP platforms operating in the European market.Define and activate data segments and audience targeting strategies to maximize campaign relevance and performance.Monitor campaign delivery and performance against agreed KPIs, proactively identifying opportunities to optimize targeting, bidding, budgets, and campaign execution.Take ownership of the percentage of campaigns achieving their agreed performance KPIs, driving continuous improvement in campaign effectiveness.Develop performance reports, analyze campaign results, and translate data into actionable insights and learnings to improve future campaign performance.Establish best practices for campaign implementation, optimization, measurement, and reporting across CTV performance campaigns.What makes you a great fit:10+ years of professional experience in digital advertising, programmatic media, performance marketing, or a related field.At least 3 years of hands-on experience managing the implementation of CTV performance campaigns using one or more relevant DSP platforms in the European market.Strong understanding of the CTV advertising ecosystem, programmatic buying, audience segmentation, and performance optimization.Proven ability to analyze campaign data, identify performance drivers, and implement optimization strategies.Experience in performance reporting, campaign measurement, and translating results into actionable recommendations.An entrepreneurial mindset, with a proactive, solution-oriented approach and the ability to thrive in a fast-paced environment.Excellent communication and stakeholder management skills.Fluent in English.University degree in Marketing, Business, Advertising, Data Analytics, or a related field.Reasons to apply:Centrally located office in the heart of Barcelona, with public transportation nearbyCompetitive compensationPrivate health insuranceFriendly, diverse, and international work environmentOpportunity to work outside of your comfort zone and develop professionally in an exciting and fast-growing CTV industry.Change the future of TV! A unique opportunity to join a well-funded, high-growth company in the early stages to help shape a product/business that will impact millions.#J-18808-Ljbffr

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others. Job Description Summary The Clinical Site Payment Associate Manager will be part of the team responsible for managing and advancing Investigator Payments. The successful candidate will possess end-to-end knowledge of the clinical site payment process and consistently provide customer-oriented support. Key Responsibilities Process investigator and site payments in compliance with applicable procedures, regulations, contracts, and country-specific requirements. Compile and review data from multiple sources, including but not limited to study budgets, EDC, and CTMS systems. Review site invoices, when required, and investigate, resolve, and respond to any issues or findings. Perform reconciliations and prepare accurate payment accruals and forecasts. Develop and maintain standard reports. Drive process, system, and reporting improvements, including evaluating opportunities for the adoption of Artificial Intelligence within Clinical Payments. Identify, assess, and manage operational and financial risks related to site payments. Collaborate effectively with internal and external stakeholders. Create, maintain, and/or collect process, project, and financial documentation as required. Education and Experience Bachelor's degree or higher in Business, Finance, Accounting, or a related field. Minimum of 5 years of experience in clinical payments. Knowledge, Skills, and Abilities Proficiency in English, both written and verbal. Strong financial, analytical, critical-thinking, problem-solving, and multitasking skills. Strong attention to detail. Ability to analyse data efficiently and present practical solutions and recommendations. Ability to work effectively in a global environment. Ability to quickly learn and adapt to new systems and processes. Strong customer-oriented mindset and service approach. Ability to collaborate effectively with cross-functional internal and external teams. Good knowledge of and experience with MS Office, financial systems, EDC, and CTMS platforms. Contract Type Regular Salary Range The final offer will be determined within the applicable location-specific range and will depend on the candidate’s confirmed work location, relevant experience, skills, qualifications, internal equity, and role scope. 45-65k Euro (Italy, Spain) Germany : 60-85K Euro gross annually. About Alira Health Alira Health is a global advisory firm providing consulting and research and clinical development services whose mission is to humanize healthcare and life sciences, in partnership with patients, through innovative technologies and expert guidance. From development to medical care, we complement the expertise of our Pharma, Biotech, and MedTech clients with a full spectrum of services across their entire solutions lifecycle. With offices around the world, Alira Health provides a vibrant and creative environment with benefits that include professional development, global travel, flexible work programs and more. We welcome your passion and drive, talent and entrepreneurial spirit, sense of service and teamwork. We are an integrated team of over 800 scientists, strategists, economists, clinicians, and biostatisticians representing over 30 nationalities. This broad global perspective and cultural richness has a direct impact on providing innovative solutions for our clients that lead to higher standards of care and an improved patient experience. #J-18808-Ljbffr

START Center for Cancer Research (START) is the world's largest network of Phase I clinical trial centers, dedicated exclusively to oncology research. Since its inception, START has provided hope to cancer patients across global communities by offering access to cutting-edge clinical trials in the United States and Europe. About the Role We are seeking a highly analytical and collaborative Clinical Business Operations Manager, to serve as the critical link between Clinical Operations and Finance. This strategic role ensures that all clinical trial activities are accurately documented, reconciled, and translated into revenue-generating transactions while maintaining the highest standards of data integrity and compliance. The successful candidate will oversee the accuracy of clinical research operational data, support billing dispute resolution, drive cross-functional collaboration, and help ensure that services performed within clinical trials are properly captured, validated, invoiced, and ultimately collected. This position is ideal for a professional with experience in both clinical research operations and healthcare revenue cycle processes who enjoys solving complex problems, improving processes, and working across multidisciplinary teams. Key Responsibilities Ensure the accuracy, integrity, and reconciliation of clinical research data across CTMS and related systems. Serve as the primary resource for sponsor and CRO billing inquiries, invoice disputes, and revenue-related investigations. Collaborate with Clinical Operations, Research Nursing, Pharmacy, Regulatory, Finance, and Revenue Cycle teams to support accurate documentation, billing, and revenue capture. Investigate and resolve operational, clinical, and financial discrepancies to minimize revenue leakage and ensure compliance. Monitor study-level invoicing, payments, aging accounts, and revenue performance, identifying risks and escalation needs. Develop and track key performance indicators (KPIs) related to data quality, billing accuracy, and operational effectiveness. Lead reconciliation, audit, and process improvement initiatives to enhance data quality, operational efficiency, and financial performance. Provide operational insights and reporting to support decision-making, forecasting, and continuous improvement efforts. Act as a liaison between internal stakeholders, sponsors, and CROs to ensure alignment, issue resolution, and successful study execution. Key Requirements Qualifications & Experience Bachelor's degree in Business Administration, Healthcare Administration, Finance, Health Sciences, or a related field. 3+ years of experience in Clinical Research Operations, Clinical Research Finance, Healthcare Revenue Cycle, Healthcare Operations, or related areas. Experience working with Clinical Trial Management Systems (CTMS), preferably OnCore. Proven ability to reconcile data across multiple systems and resolve operational discrepancies. Experience working in a regulated healthcare or clinical research environment. Preferred Qualifications Experience in Phase I Oncology Clinical Research. Knowledge of sponsor billing, clinical trial revenue processes, and study financial workflows. Experience partnering with sponsors, CROs, and finance teams. Professional certifications such as CCRP, CRA, ACRP, or equivalent clinical researchcredentials. Key Competencies Strong analytical, problem-solving, and root-cause analysis skills. High attention to detail with a commitment to data accuracy and integrity. Excellent communication and stakeholder management skills. Ability to collaborate across clinical, operational, financial, and external partner teams. Strong organizational, project management, and prioritization abilities. Continuous improvement mindset with experience using KPIs to drive performance. Understanding of compliance, risk management, and regulatory requirements. Why Join START? At START, you will have the opportunity to contribute directly to groundbreaking oncology research while helping ensure operational excellence and financial sustainability. If you are passionate about data integrity, operational excellence, clinical research, and revenue optimization, we invite you to join our mission of advancing cancer treatment and improving patient outcomes worldwide. #J-18808-Ljbffr

Agilent Technologies is seeking an experienced SAP Tax Technology professional to drive design, implementation, and optimization of indirect tax solutions across a global SAP landscape. You will bridge Tax, Business Partners, and IT to architect scalable, automated tax solutions using SAP ECC, S/4HANA, and DRC. The role emphasizes end-to-end SAP project delivery, cross-functional collaboration, and global compliance initiatives, with a focus on VAT, GST, and other transactional taxes. #J-18808-Ljbffr

Responsibilities Serve as a statistical department resource Conduct training sessions and enhance skills of existing personnel Collaborate with the sponsor and review project work produced by other statisticians Manage multiple projects and ensure timely completion Requirements Experience mentoring biostatisticians on job skills Experience preparing Statistical Analysis Plans (SAPs) Knowledge of SAS annotated case report forms (CRFs) and SAS database design Ability to oversee training plans or materials for Biostatistics associates Proven statistical programming skills Experience conducting quality control of project deliverables #J-18808-Ljbffr

At TRKKN, we are driven by the excitement of taking our client's data-driven businesses to new heights. As the leading European Google partner and reseller of Google Cloud & Google Marketing Platform, we act as a catalyst for cutting-edge digital marketing solutions. Our team is diverse, international, inspiring, and operates in a fast-growing digital & technological environment. This provides the ideal and dynamic work environment for individuals with a hunger for growth, responsibility, and the desire to shape their future. With Google in close proximity, the learning and development opportunities at TRKKN are limitless. With over 25 nationalities, 20+ languages, and 240+ Trakkies on board, we’re taking our business global, and our story doesn't end here! How will you make an impact: As the Tech and Data Strategy Lead (f/m/d) in Spain, you will play a central role in connecting people, data, and technology. You will lead client strategy, drive digital maturity for all type of clients by systematically identifying levers and technical solutions across the Google Marketing Platform and Google Cloud. Your key responsibilities will include: Pre-Sales & Commercial Strategy: Lead pre-sales activity for new business opportunities, commercial proposals, opportunity analysis, and cross-selling/upselling for existing clients in Spain. Solution Packaging & Tech Strategy: Define sales strategies and package solutions (incrementality, measurement frameworks, 1st party data strategies, privacy, and tech stacks). Strategic Consulting & Workshops: Conduct Tech & Data Maturity Assessments and lead Strategy Workshops for key clients to solve complex business challenges in an evolving privacy-centric ecosystem. Key

Biorce is seeking a Technical Talent Acquisition Partner to scale our engineering, AI, data science, and product teams from our Austin hub. You will own the full recruitment lifecycle, partner with hiring managers, and build pipelines in a fast‑growth Healthtech AI company. You should be fluent in English, experienced in sourcing for senior technical roles, and comfortable operating in a high‑velocity environment, using LinkedIn Recruiter, ATS, and other tools to outpace competition. #J-18808-Ljbffr

ANYbotics is a fast-growing tech company dedicated to shaping the future of mobile robotics across multiple industries. Join our highly talented and motivated team of more than 200 people and work on cutting-edge robot technology. The Opportunity As Technical Program Manager, you will lead the delivery of one of ANYbotics’ most strategically important robot platform programs, bringing engineering, operations and commercial teams together around a clear and credible path to market. You will carry delivery accountability against the agreed specification, schedule and product-cost targets, providing one clear and credible view of the program. Working closely with Product and Engineering, you will translate agreed product and technical decisions into an executable plan across mechanical and electrical engineering, software, industrialization, supply chain, certification, quality, service and launch readiness. This is a highly visible, hands-on leadership role. You will combine strong technical understanding with excellent program judgement, moving comfortably between detailed engineering discussions and executive-level decisions. You will bring clarity where information is incomplete, identify emerging risks and create the momentum needed to make difficult trade-offs at the right time. You will operate as a senior individual contributor, focusing on one major program at a time and leading through influence rather than direct authority. You will work closely with functional leaders and named workstream owners, while having the opportunity to strengthen how ANYbotics runs complex product development and help shape our broader program-management capability as the company grows. Market & Our Technology ANYbotics is pioneering autonomous robotic platforms for industrial inspection and operations in challenging environments. From explosion-proof systems in oil and gas to agile robotic platforms for power, utilities, mining, metals and other industrial settings, our technology is built for environments where safety, reliability and uptime are critical. Our product combines advanced robotics, mechanical and electrical systems, embedded software, autonomy, inspection payloads, analytics and integrations into an end-to-end industrial solution. Bringing a new robot platform to market requires hardware and software development, industrialization, supply chain, certification, quality and customer readiness to progress together. This creates a distinctive program-management challenge. Long hardware lead times must be balanced with iterative software development, ambitious product goals, demanding certification requirements and complex make-or-buy decisions. Strong technical program leadership is essential to turning this complexity into reliable execution. About us ANYbotics is a leading robotics company specialising in advanced autonomous systems. With a successful Series B financing round closed and strong momentum in the market, we are entering an important phase of growth and international expansion. Our mission is to transform industrial inspection and operations through world-class robotics. We combine deep robotics expertise with real customer deployments in demanding industrial environments. This is an opportunity to join at a stage where the technology is proven, the ambition is high, and the decisions made now will have a major impact on the company’s future. Your Contributions Lead an integrated robot platform program from charter through development, industrialization, launch, early-life reliability and handover, delivering against agreed specification, schedule and product-cost targets Own the integrated program plan against the agreed scope, including the baseline, milestones, dependencies, critical path, COGM targets and delivery gates Align work across hardware, software, industrialization, supply chain, certification, quality, verification and validation, service and launch readiness, maintaining one credible view of progress for senior stakeholders Work through functional leaders and named workstream owners to establish clear responsibilities, identify capability gaps and secure credible delivery commitments Identify risks and cross-functional trade-offs early, bringing forward practical options with their technical, cost and schedule implications, together with a clear recommendation Drive evidence-based program reviews and consolidated delivery readiness across quality, certification, service and launch, adapting the plan early when assumptions or technical evidence change Partner with Product and Engineering to translate agreed requirements into an executable delivery plan, including the certification and country sequencing needed to support launch Work with the CTO and Operations on make-or-buy decisions, industrialization and external-partner execution, ensuring clear interfaces, commitments and acceptance criteria Your Profile Significant experience leading complex technical programs in robotics, autonomous systems, industrial technology, automotive, aerospace, medical devices or another advanced hardware environment Proven experience shipping a certified, volume-manufactured mechatronic product and leading it through development, industrialization and commercial launch Strong engineering foundation in mechanical, electrical, mechatronic, robotics, systems engineering or a similarly relevant discipline Technical depth to understand system architecture, challenge senior technical specialists and recognise system-level risks without needing to design every solution personally Strong command of program-planning methods, critical-path management, structured product-development processes and disciplined change control Practical experience across product cost, industrialization, manufacturing, supply chain, quality, certification and external technology or manufacturing partners Proven ability to influence senior technical and business stakeholders, resolve competing viewpoints and create alignment without relying on direct authority Decisive, resilient and highly organised, with the judgement and communication skills to operate effectively in a fast-moving environment and make progress with incomplete information Bonus Points Direct experience delivering industrial robots, autonomous machines or other complex mechatronic systems Experience with products operating in safety-critical, hazardous or highly regulated environments Experience developing a new product through platform reuse, architectural evolution or a tightly controlled derivative program Experience with international product certification, including CE, UL or comparable market-access requirements Experience transferring products from prototype or internal production into serial production with an EMS, ODM or other external manufacturing partner We offer you a very exciting and dynamic work environment, the opportunity to become part of a fast-growing company and an ambitious team that is on a mission to change the industrial inspection market, a chance to leverage your experience and bring in your own ideas, a fair market salary, an attractive employee stock ownership plan, and a job in the city of Zurich. Agency Policy: We are not currently partnering with external search firms or recruitment agencies. Any profiles or resumes submitted to ANYbotics employees without a prior written agreement will be considered public disclosure and the property of ANYbotics, involving no liability or fee for subsequent hiring.

The Apex Group was established in Bermuda in 2003 and is now one of the world’s largest fund administration and middle office solutions providers. Our business is unique in its ability to reach globally, service locally and provide cross-jurisdictional services. With our clients at the heart of everything we do, our hard‑working team has successfully delivered on an unprecedented growth and transformation journey, and we are now represented by over circa 13,000 employees across 112 offices worldwide. Your career with us should reflect your energy and passion. That’s why, at Apex Group, we will do more than simply ‘empower’ you. We will work to supercharge your unique skills and experience. Take the lead and we’ll give you the support you need to be at the top of your game. And we offer you the freedom to be a positive disrupter and turn big ideas into bold, industry‑changing realities. For our business, for clients, and for you. Apex Risk Technologies (ART) is a leading fintech firm and a critical part of the Apex Group, a global financial services provider. ART clients include alternative investment funds, banks, and fund management companies (ManCo’s). At ART, we have a passion for finance and technology with a strong commitment to research and development to continuously innovate and improve client solutions within an open and collegiate environment. ART’s core solution is RiskMonitor®, which provides an independent appraisal of investment risk compliance and financial risk exposures. RiskMonitor® produces customisable risk reporting suitable for boards, risk committees, and investors as well as risk data required for regulatory submissions. ART is a fast‑growing business and we are looking for a Junior Quantitative Developer to join our team in Barcelona. In this role, you will liaise with Portfolio Managers, Risk Managers and Investment Analysts to onboard their funds in RiskMonitor®, develop bespoke solutions and be involved in the daily maintenance of their accounts. In addition, you will closely work with the quantitative development team in Barcelona and Apex technology management colleagues globally to ensure the successful evolution of the ART business unit within Apex. Lastly, you will collaborate with business partners, technology vendors, client counterparties, and colleagues within the Apex Group. This role would suit someone who’s seeking a career in finance and technology with a keen and demonstrable interest in quantitative finance. Job responsibilities Key Development Initiatives Annex IV and Form PF: Refactor and further develop existing code base and solutions to facilitate best in class stand‑alone solutions New report parts and analyses: Liaise with clients to understand requests and their feasibility Product & Operations Liaison Performance analysis reconciliation (Performance, Factsheet metrics, Contribution/Attribution, Exposures, etc.) Work with colleagues from Apex Offices globally to ensure correct liaison and delivery including but not limited to BAU across restriction queries, report related queries, admin issues Ensure that methodology is well explained, present RiskMonitor® new features to clients, and assist both clients and colleagues from other Apex Offices during the onboarding phase Coordination and liaison on VaR, performance, market risk and liquidity risk metrics Partner and client liaison Support general client and partner initiatives globally Role Requirements Working knowledge of MATLAB and SQL Server Demonstrable source control experience ideally with both GIT and SVN Good business acumen and sound finance knowledge Excellent communication skills (English) Desirable Attributes Interest in MATLAB Demonstrable interest in quantitative finance Keen to pursue professional certifications (CFA, FRM, etc.) #J-18808-Ljbffr

ADP seeks an experienced Portfolio Manager to lead enterprise programs across the International Product portfolio. You will partner with GPTs, corporate functions, and stakeholders to drive governance, prioritization, and execution. Strong Agile and leadership skills are essential for executive reporting and global collaboration. The role requires building dashboards, driving change, and delivering measurable business outcomes while navigating complex multinational environments. #J-18808-Ljbffr

Senior Toxicologist – Contract (Remote or On-Site, Spain) Location: Spain (Remote or On-Site) Contract Type: Freelance/Contract Experience: 12+ years Overview Our client is initiating a major project in Spain and is seeking an experienced Senior Toxicologist to provide high-level scientific leadership on a contract basis. The ideal consultant will bring deep expertise in toxicology and non-clinical safety, supporting strategic input across complex development activities. Key Responsibilities Lead and advise on non-clinical toxicology strategy across development programs Design, review, and interpret toxicology studies Prepare or contribute to regulatory documentation Support regulatory interactions as needed Collaborate effectively with cross-functional teams Requirements Minimum 12 years’ professional experience in toxicology Strong background in non-clinical safety assessment Proven experience in study design, data interpretation, and strategy Regulatory submission experience highly beneficial Ability to work independently and proactively What We Offer Flexible setup: fully remote or on-site in Spain Opportunity to contribute to a high-visibility international project #J-18808-Ljbffr

ABOUT US At STADA we pursue the purpose of "Taking care of people's health as a trusted partner." All our decisions and actions are driven by our purpose, vision and values. With our wide range of products: Generics, Consumer Healthcare and Specialties, we offer patients, doctors and pharmacists a wide range of therapeutic options. Around 13,000 employees live our values of Integrity, Entrepreneurship, Agility and One STADA, in order to achieve our ambitious goals and shape a successful future for our company. We continually expand our goals in line with our ambition, and we achieve them with passion, commitment and a growth mindset. Do you want to be part of a successful international pharmaceutical company and grow with us? Manager Global Technology Transfer is responsible for leading end-to-end Technology Transfer execution providing Project Management, scientific and technical expertise, e.G., in quality, technology transfer, regulatory. KEY RESPONSIBILITIES Lead and manage Tech Transfer projects effectively and independently, ensuring deliverables are completed in time, at agreed costs and carefully balancing benefits & risks Define Project strategy, Project Team and create end-to-end Project Plan capturing project risks including mitigation strategy Coordinate cross-functional Project Team across internal stakeholders (Global and local TechOps functions: QA, QC, AS&T, MS&T, ESO, RA, Commercial Transfer Team), as well as the third parties wheninvolved in the project scope (CMOs) e.G. transfer Projects to the Contract Manufacturer Run project meetings to monitor project milestones, track project execution and report on progress Ensure cross-functional alignment and joint decision-making, define actions in project meetings and follow up on execution with project team members Provide scientific and technical expertise, e.G., in quality, regulatory, tech transfer and resolve issues which occur as part of daily business to ensure cross-functional information flow on the way to adhere to the project schedule Consolidate Master Documentation (Technical Package) for BC calculation and provide technical expertise on transfer feasibility to the target site Check that content of GMP documents is correct and complete and in compliance with the dossiers Support manufacturing sites to produce trial and validation batches (provide onsite support) Write Product Performance Review – Report after feasibility trials that summarizes conclusions and recommendation for validation batches Prepare the updates to Module 3 according to technology transfer results Prepare the variation documentation in accordance with local regulatory requirements of impacted countries Support product launches from the new site following transfer in cooperation with Commercial Transfer Team, Supply Chain, QA, RA. EXPERIENCE University degree in Pharmacy, Chemistry/Chemical Engineering, Biology (Life Sciences) or comparable field Fluent in English (written and spoken) More than 5 years of work experience in Pharma Industry (in depth knowledge preferably in technology transfers, product development, manufacturing, or regulatory affairs). It can independently manage all areas of Tech Transfer Projects: quality, regulatory and technical Project management experience and capability to lead multi-functional teams Learning agility – as ongoing, proactive, and self-motivated pursuit of knowledge Business/market/technology savvy - understanding business and impact on business Growth mindset- sees obstacles as surmountable challenges Strong problem solver with the ability to multitask and make sound decisions in a fast-moving environment Integrity as concept of consistency of actions, values, methods, measures, principles, expectations, and outcomes Open to travel globally flexibly STADA Group STADA Group promotes its diverse culture, regardless of gender, age, social or ethnic origin, disabilities, religion, ideology or sexual orientation. We use the strength of this diversity to develop creative ideas, Expand our experience and increase innovative strength. Our focus is on equal opportunities, respectful cooperation and the promotion of an inclusive working environment. STADA STADA offers a competitive environment for personal and professional development in a growing company full of opportunities. Our future project requires dynamic and proactive professionals, capable of adding value in a changing environment. Follow us on LinkedIn to receive our news! #J-18808-Ljbffr

Seeking Dentists, General Practitioners and Specialists in Orthodontics/Prosthodontics for private practices in Ireland. Requires a Bachelor in Dental Surgery and advanced English. Offers competitive salary and relocation support.

Clinical Monitoring Analyst (Cluepoints) - Remote London, United KingdomBudapest, HungaryReading, Berkshire, United KingdomBloemfontein, South AfricaDublin, IrelandCenturion, South AfricaBarcelona, SpainSofia, BulgariaMadrid, SpainFull timeR This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills. Having experience with SAS programming is necessary.This role is part of a sponsor dedicated project where you will be working with the client directly to manage deliveries. The CMA contributes to the execution of the Centralized Monitoring process by performing the setup, programming and refresh(es) of the Centralized Monitoring platform, according to the study-specific Centralized Monitoring Plan (CMP). Supports the Centralized Monitoring Lead (CML) in the development of the fit-for purpose CM strategy by contributing to the identification of the relevant CM elements to be implemented for the study (Quality Tolerance Limits (QTL), Key Risk Indicators, data visualizations and Data Quality Assessments) Setup/Program QTL, KRI and Data Quality Assessments according to the study CMP Refresh the Centralized Monitoring Platform at predefined frequency to enable signal identification Generate and maintain the Centralized Monitoring Platform specifications document and file it in eTMF Review and understanding of protocol is key Understand the data sources for the study, the data transfer specifications and the data structure Execute and document peer-review of CM platform setup done by other CMA colleagues Experience: At least 3 years relevant experience in the area of pharmaceutical research and development or related field preferably in centralized Monitoring, data management, and/or biostatistics 2-3 years SAS experience including macro language Knowledge/ experience working on Cluepoints Ability to work in an autonomous way and engage with relevant stakeholders to execute activities related to study level centralized monitoring process. Ability to understand basic statistical analysis concepts and to interpret their outcome. Ability to maintain confidentiality of data and information during interactions with staff at all levels Ability to work with limited close supervision. Demonstrated communication, interpersonal, organizational and problem-solving skills High levels of initiative, drive and commitment. Prior experience in a Data Management related field is required Experience with relational databases, preferably Clinical Data Management and EDC Systems Experience communicating with all levels of personnel and participating in collaborative work team (locally and globally). Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices. Excellent command, both verbal and written, of English This role is not eligible for UK visa sponsorship IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. ... (company culture and EEO statements omitted for brevity) #J-18808-Ljbffr

Company Description At Docplanner Group, we’re on a mission to help people live longer, healthier lives. As the world’s largest healthcare platform, each month, we connect 24 million patients with 280k doctors across 13 countries (through brands like ZnanyLekarz, Doctoralia, MioDottore, DoktorTakvimi, and jameda). Our marketplaces, SaaS and AI tools simplify daily tasks and help doctors, clinics and hospitals work more efficiently, so they can focus on what really matters: caring for their patients. Learn more about our products here: pro.Doctoralia.Es Why join us? Real impact – We help doctors help patients. Your work truly makes a difference. At scale, yet agile – 3,000+ employees, but still fast, flexible, and hands-on. Shape the future, sustain growth – Make a difference now and build for long-term success. Job Description How will you make an impact? Job Purpose As Patient Care Regional Manager, you will be the people manager and operational lead for Patient Care teams in your assigned European markets. You will own team performance, quality reviews, and day-to-day operations — while working closely with Country Managers and the Global Patient Care Head to align on priorities and ensure service consistency across markets. You will be the missing link between global standards and local execution: someone who can read data, give direct feedback, run a tight operational cadence, and genuinely develop the people on your team. Key Responsibilities People Management Own performance reviews, 1:1s, and development conversations for direct reports across your markets Manage absence, availability, and team sizing for your region Lead hiring decisions and internal mobility within the Patient Care team Build a culture of direct feedback and consistent follow-through Operational Performance Track and own regional KPIs: response SLA, first-contact resolution, CSAT, and quality scores Run quality review and moderation programs — calibration sessions, rubric definition, feedback loops Identify performance trends using dashboards and reports; translate them into concrete actions Own escalation protocols for complex patient cases Cross-functional Collaboration Partner with Country Managers to align on priorities, workload, and service commitments Work with the Product/PATS team on tooling rollouts, workflow automation, and process improvements Contribute to the monthly Patient Voice reporting — classified ticket analysis, actionable issue surfacing Act as regional interface for global policy rollouts and operational changes Qualifications What will help you thrive? Must-haves 5+ years in customer support, patient experience, or service operations — with at least 2 years managing people Experience managing teams across multiple countries in Europe (not just one market) Strong people instincts: direct, empathetic, consistent — someone teams trust and grow under Data-driven: comfortable with dashboards, pulling operational reports, and making decisions from numbers Experience running quality review or moderation programs (calibration, rubric design, scoring) Fluency in English mandatory Proficiency in project management tools (e.G., Jira, Notion, or similar) Nice to have Background in healthtech, marketplace, or two-sided platforms Experience working with AI-assisted support tools or automation workflows Familiarity with Intercom, Zendesk, or equivalent support tooling SQL knowledge or comfort querying data independently Experience onboarding a new org structure or consolidating teams Strong plus — Spanish, Italian, Polish, or German language speaker. What To Expect From Our Hiring Process Intro Chat A first call with our Talent Partner to explore mutual fit around relevant skills, value alignment, and motivation. Hiring Manager Interview A deeper conversation about your background, aspirations, and experience with your Hiring Manager and your potential manager in this role. Take this chance to ask anything on your mind—it’s just as much about making sure we’re the right fit for you, too. Business Case A take-home exercise incl. a few days' preparation time, designed to understand how you approach real-life problems. You’ll then walk us through your approach in a collaborative discussion with the hiring manager and the team to discuss your thoughts and findings. Additional/ Final Interview (Optional) A final conversation with another senior stakeholder from our Global Team. Why You’ll Love It Here Global Benefits Healthcare insurance – so you can focus on what matters. Wellness that works for you – from gym memberships to mental health support, we’ve got you covered. Time off that counts – whether it’s a vacation, your birthday, or just a day to recharge, we believe in balance. Local Perks Depending on your location, you will be entitled to local benefits like meal vouchers (ticket restaurant), transport allowances, or extended parental leave. Career Growth We’re growing, and so can you! You’ll find lots of chances to learn, develop, and explore new paths—whether within your team or through cross-functional projects. A Truly Global Team Work with talented people from all over the world in a diverse and inclusive environment. Flexibility That Works for You Remote work and flexible hours aren’t just buzzwords here. While the extent of flexibility depends on your role and team, we value results over rigid schedules. Prefer an office setting? You're welcome at any of our hubs in Barcelona, Warsaw, Curitiba, Rio de Janeiro, Mexico City, Bogotá, Munich, Rome or Bologna. What We Believe In Focus on results – we're here to make an impact. Think like an owner – take responsibility, drive outcomes. Keep it simple, keep it lean – smart solutions over complexity. Be respectful and radically honest – openness builds trust. Learn and be curious – growth is part of the job. We are committed to building a team that represents a variety of backgrounds, perspectives, and skills. We welcome applicants from all walks of life, regardless of gender, disability, or background, and are dedicated to fostering an inclusive workplace where everyone feels valued and empowered to contribute. Please note: At this time, we are not able to sponsor visas for this position. To apply, you must already have the legal right to work in your country of residence or the location of the role. #J-18808-Ljbffr

Sponsor Dedicated Global Sr CTM - Home Based in SPAIN. Vendor experience Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health: We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.Job ResponsibilitiesProtocol Development: Support the development and review of the Clinical Study Blueprint (CSB) and Protocol, and all Amendments and/or Administrative Changes Budget: Manage the execution of the CDAs; support Project Managers in the creation of overall study budget (working with the contract/budget analyst); support site contract amendments and negotiation; manage invoices Countryand Site Feasibility and Selection: assist in development of Investigator Site Selection Plan; attend country and siteselection Jams; Assist with creation ofFeasibility Questionnaire; assist with Site Selection and Green Light Letters, if applicable Site/Country Contracts and Budgets: stay informed of progress with CDAs, CSA and site budgets; support sites forcontract amendments; assist with negotiationfor site contracts Financial/Payment Management: oversight of site payments and vendor payments, if applicable Study Budget Financial Reconciliation: draft and facilitate the Clinical Study Budget review Clinical Study Timelines: Support the planning for the clinical study timelines, finalization and update of clinical study timelines; and manage the study team to meet all timelines Study Team Training: Assist/support in the creation/finalization of Study Specific Training (TA training, Compound, Study Design, Vendors, Eligibility, etc); Facilitate training sessions; Assign training as appropriate; assist with creation/finalization of Study Monitor Training materials Site Training: Assist Project manager in planning for the Investigator Meeting; creation of and collection of slides from all functional areas to create the final master deck for the IM; presenting at theIM, filing documentation of training Data Management and Closeout: Review updates to Data Managemet Plan; Interim/Final Db Lock Preparation (drive study DBL completeness); Interim/Final Database Lock Preparation (Responsible for study DBL completeness) Plans: Site Selection Plan, Study-Specific Issue Management Plan, Vendor Oversight Plan, TMF Artifact Map and Plan Clinical Supplies: Assess and review of materials by external vendors (lab kits, ePRO devices, eConsent tablets, etc); Investigational Product: responsible for overall study reconciliation of IP Vendor Oversight: Assist with selection of vendors; Create and manageVendor Oversight Plan for each vendor; review vendor contracts, work orders and Change Orders; day to day oversight ofvendors Establish Review Committees: creating charter, assisting with member selection, contracting as needed, updating Annual Plan Site Closure Strategy: develop site closure plan Patient Recruitment Strategy: assist Project Managers in development of patient recruitment strategy and plan; develop recruitment materials; drive strategies for needing new sites Trial Master File: support customization of study/country/site specific docs; upload documents,reference Master File Index; oversight of TMF health; TMF reconciliation; TMF archival; quarterly TMF review Risk Management: initial Risk Assessment and Mitigation Plan (RAMP) and maintain throughout study; responsible for Issue Management throughout the study; quarterly Issues reviewICF and Study Specific Language: responsible for building the study specific ICF incorporating appropriate study specific language and safety language CTA submissions and approvals: responsible for assisting with agency responses Meetings: Clinical Study Team meetings, conducting vendor meetings; responsible for agendasand meeting minutes Clinical Trial Management System: Keep CTMS updated at study levelQualificationsBachelor’s degree or RN in a related field or equivalent combination of education, training, and experience 5 years or more of experience as CTM, managing multiple countries, for regional or global trials Proven vendor management experience. Global study management experience. Experience in Oncology clinical trials. Strong experience reviewing and overseeing study plans and study-related documentation. Demonstrated ability to lead and align teams in the achievement of project milestones Demonstrated capability of working in an international environment. Demonstrated expertise in site management and monitoring (clinical or central)Preferred experience with risk-based monitoring Demonstrates understanding of clinical trial management financial principles and budget management Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements Must demonstrate good computer skills Strong conflict resolution skills Demonstrated ability to apply problem solving techniques to resolve complex issues and apply a risk management approach to identifying and mitigating potential threats to the successful conduct of a clinical research project. Demonstrates critical thinking to determine the cause and appropriate solution in the identification of issues Moderate travel may be required, approximately 20%Additional InformationTasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.Discover what our Syneos Health colleagues already know: work here matters everywhere. Work alongside the brightest minds in the biopharmaceutical industry taking down walls and removing barriers to speed our customers’ delivery of important therapies to patients. We are strategic thinkers who actively seek different perspectives, whether across offices or across oceans. Because we solve some of the toughest challenges facing the most prestigious healthcare companies today, you'll gain exposure and be supported with comprehensive resources including emerging technologies, data, science and knowledge sharing. The diversification and breadth of Syneos Health creates a multitude of career paths and employment opportunities. We’re a growing, global company dedicated to advancing our talent past their initial role. Discover what our 29,000 employees already know: work here matters everywhere. We work hard, and smart, all in the name of getting much-needed therapies to those who need them most. Selecting us as an employer secures a career in which you’re guaranteed to: Partner with the most diverse team of experts in the industry. From the top down, our people are inspiring. Everyone has a voice and is encouraged to use it. Work in specialized Syneos Health teams that are therapeutically or functionally aligned for expert collaboration. We assemble clinical teams where everyone, from CRAs to senior management, is skilled in the same therapeutic area or customer teams. With this structure, everyone on your team speaks the same language and can deliver unique insights into the therapeutic environment and patient population. We are partners with purpose. We integrate seamlessly with our customers and do what’s best for their success. Our people provide the brilliant ideas, valuable insights and endless energy that accelerates the impact of life changing therapies worldwide.#J-18808-Ljbffr

GE Vernova invites applications for ROC Technical Lead in its Wind Remote Operations Center in Barcelona. The role focuses on monitoring offshore wind assets, remote diagnostics, and coordinating with site teams to resolve issues and optimise performance.The position requires a engineering degree, wind industry experience, SCADA tool familiarity, and the ability to travel up to 20% with willingness to relocate to Barcelona. Fluency in English is essential.

Seeking a Principal Engineer/Tech Lead & Systems Architect in Barcelona with 15+ years of experience in web development, PHP, and JavaScript frameworks, to lead complex engineering projects.

Medical Scientist (m/f/x), Nephrology & Patient Blood Management Location: Barcelona Contract: permanent The Opportunity We are looking for a Medical Scientist, Nephrology & Patient Blood Management (PBM) to join our Medical Affairs organization in Spain. This is an exciting opportunity for a scientific professional who wants to work at the intersection of medical strategy, evidence generation, stakeholder engagement and healthcare innovation. In this role, you will translate scientific evidence, real‑world data and stakeholder insights into meaningful Medical Affairs strategies, helping to identify unmet needs, close evidence and care gaps, and ultimately improve outcomes for patients within nephrology and Patient Blood Management. We will prioritize candidates based in Barcelona. However, exceptional candidates located elsewhere in Spain will also be considered, provided they can meet the requirements of our hybrid working model. The Role As Medical Scientist, you will act as a trusted scientific partner, combining scientific credibility with strategic thinking and strong stakeholder engagement. Your key responsibilities will include: Provide scientific leadership across nephrology, rare kidney diseases and Patient Blood Management, including areas such as coagulation and iron. Build and maintain trusted relationships with Key Opinion Leaders (KOLs), healthcare professionals and other relevant external stakeholders. Translate scientific developments, stakeholder perspectives and emerging evidence into actionable medical insights and strategic recommendations. Identify unmet medical needs, evidence gaps and opportunities to advance patient care. Contribute to evidence-generation activities, including Investigator-Initiated Studies (IIS), research collaborations and real‑world evidence initiatives. Support the development and execution of Medical Affairs plans in close partnership with internal and external stakeholders. Develop and support congress strategies, scientific communications, medical education initiatives and scientific exchange. Explore the use of real‑world evidence, data analytics and AI-enabled approaches to strengthen Medical Affairs insights and decision-making. Collaborate closely with colleagues across Commercial, Market Access, Regulatory and Clinical Development to support aligned, patient‑centric medical strategies. Success in this role means turning scientific insights into strategic action, influencing medical and organizational decisions, building trusted external partnerships, and helping to close evidence and care gaps through science and innovation. Your Qualifications To be successful in this role, you bring: An MD, PhD, PharmD or equivalent advanced scientific qualification. 3–5+ years of relevant experience within Medical Affairs, Medical Science Liaison, Clinical Research or a related pharmaceutical industry role. Previous experience within nephrology, cardio‑renal diseases, coagulation, iron, rare diseases or specialty care. Experience supporting scientific exchange, evidence generation, Investigator‑Initiated Studies and medical education initiatives. Demonstrated ability to collaborate effectively with cross‑functional partners, including Commercial, Market Access, Regulatory and Clinical Development. Familiarity with the Spanish healthcare environment. Excellent communication, scientific exchange and stakeholder engagement skills. A strategic mindset with the ability to translate complex scientific information and stakeholder insights into meaningful actions. Fluency in Spanish and English. What We Offer We want you to feel supported professionally and personally while making a meaningful contribution to patients and healthcare. The opportunity to contribute to Medical Affairs strategies that can make a tangible difference for patients. A highly scientific role combining external engagement, evidence generation and strategic Medical Affairs work. The opportunity to collaborate with leading scientific experts and multidisciplinary teams in an international environment. Exposure to evolving approaches in real‑world evidence, data analytics and AI‑enabled Medical Affairs. Opportunities for professional development and continued growth within an international organization. A collaborative, purpose‑driven working environment focused on science, innovation and patient impact. A hybrid working model. The role requires at least three working days per week either in the office or engaging with external stakeholders in the field, together with occasional travel and in‑person collaboration according to business needs. About CSL Vifor CSL Vifor is a global partner of choice for pharmaceuticals and innovative, leading therapies in iron deficiency and nephrology. We specialize in strategic global partnering, in‑licensing and developing, manufacturing and marketing pharmaceutical products for precision healthcare, aiming to help patients around the world lead better, healthier lives. Headquartered in St. Gallen, Switzerland, CSL Vifor also includes the joint company Vifor Fresenius Medical Care Renal Pharma (with Fresenius Medical Care). The parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit and CSL Plasma at Our Benefits For more information on CSL benefits visit How CSL Supports Your Well‑being | CSL . You Belong at CSL. At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please click here. Privacy Notice CSL Global Privacy Notice for Job Applicants and Candidates #J-18808-Ljbffr

IC Resources in Barcelona, Spain seeks an experienced High-Speed Systems Engineer to take technical ownership of a next-generation hardware platform. You’ll work across system architecture, lab debugging, and collaboration with FPGA and software teams to deliver a complete system. The role combines hands-on hardware work with technical leadership, mentoring a growing engineering team, and driving critical decisions to ensure high-performance outcomes. #J-18808-Ljbffr

Adeas Hr busca un EXPERTO DE PROCESOS (Compounding) para liderar, transferir y poner en marcha procesos estériles de producción en una multinacional farmacéutica con foco en GMP y FDA. Coordinará lotes técnicos, media fills y actividades de transferencia, asegurando cumplimiento y documentación GMP durante todo el proyecto. El candidato ideal tiene 5+ años en industria farmacéutica, experiencia en transferencia de tecnología, y dominio de MES/SAP/TrackWise. #J-18808-Ljbffr

Se busca un consultor de talento junior para gestionar procesos de selección, entender vacantes, generar insights de mercado y colaborar en la detección de oportunidades comerciales, con formación y acompañamiento constante.

As a Senior AI/ML Platform Engineer and Technical Lead, you will be at the heart of building and evolving the AI/ML platform that powers intelligent capabilities across the organisation. Acting as a key technical liaison across Cloud, Cybersecurity, Governance, and adjacent engineering teams, you wi

IRB Barcelona is seeking a highly motivated and talented Postdoctoral Fellow to participate in cutting edge research line of the Quantitative Stem Cell Dynamics lab led by Alejo Rodriguez-Fraticelli.The lab focuses on implementing cutting-edge single-cell technologies to discover new druggable susceptibilities in leukaemia and other blood malignancies. The goal is to identify new targets to prevent drug-resistance and relapse in these terrible diseases.We are looking for a wet lab candidate with a strong background in cancer biology, epigenetic analysis and/or stem cell research. Knowledge of single-cell sequencing, clonal analysis, biostatistics, and/or genomics will be appreciated but is not required for this position and the candidates will be trained in all appropriate skills for this project.The position is for 2 years, with the potential to extend this contract up to 2 additional years. This level of support makes this an excellent opportunity for candidates looking to transition to an independent research-focused position.KEY RESPONSIBILITIESIndependently design and test biological hypotheses.Plan, perform and interpret experiments.Collaborate with a multidisciplinary research team, tapping into the expertise of fellow researchers and external collaborators.Contribute to a culture of scientific excellence, efficiency, and teamwork.Contribute to other lab projects and to the maintenance of protocols and laboratory resources in the group.Critically analyze analytical results, participate in scientific discussions and in preparation of diverse forms of scientific communication (seminars and conferences).Participate in the project activities: meetings, presentations, visits to other labs, collaboration, exchange of data sets, preparing project reports/deliverables.Perform excellent research according to the high standards of the lab and the IRB Barcelona.YOU HAVEPhD in a relevant Life Sciences field.At least one publication as first-author in a top-ranked journal (ranked Q1 in a life sciences field)Experience in hematological malignancies, including ex vivo and in vivo experiments.Demonstrated ability to design and conduct experiments independently, particularly in the area of single-cell genomics (at the very least, single-cell RNAseq).Excellent communication skills and the ability to collaborate effectively.Strong organizational and multitasking skills.Attention to detail and accuracy.Proficiency in English (both written and spoken).Highly motivated, enthusiastic and collaborative person.Willing to keep on learning.Ability to work independently in a demanding research environment.YOU MIGHT ALSO HAVEFamiliarity with acute myeloid leukemia models, including patient derived materials.Experience with CRISPR screening techniques.Experience with computational data analysis of single-cell genomics data.Ability to secure additional funding, such as grant-writing or fellowship-writing skills.WHAT WE OFFER:To be a part a part of something meaningful: We are a biomedical research centre that tirelessly works to achieve a society free of diseases. Our mission is to carry out research of excellence to cure cancer and other diseases linked to ageing.Good Working conditions:Employed in compliance with Spanish legislation and regulations under a full-time contract. Employees receive the benefits of the Spanish Social Security system covering sickness, maternity/paternity leave and injuries at work.Competitive salary: commensurate with experience and qualifications.International Environment: Nearly 90 Postdoctoral researchers (more than a half non-Spanish nationals) are currently working at IRB Barcelona.Multidisciplinary Research: Research of excellence at the unique interface between biology, chemistry, and structural and computational biology.Training and Career: Postdoctoral researchers joining IRB Barcelona gain access to the Institute’s advanced research training and career development opportunities, all within in a competitive international environment. Courses and workshops on themes of particular interest to postdocs are offered regularly by the Institute.Relocation & Visa Assistance: Trained staff provides support on visa paperwork, administrative requirements, and practical information on living and working in Barcelona, etc.Social Life: We like to have fun. We promote several activities, like a Football League, an annual skiing trip, a Mountaineering Club, a Running Club and "Cool-off sessions", where members meet informally for drinks, snacks and scientific discussions.Fairness: Our recruitment is open, transparent and merit-based, and all applicants compete on the same terms. We are an Equal Opportunity Employer and all qualified applicants are considered for employment without regard to race, colour, religion, age, sex, sexual orientation, gender identity, nationality, ethnic origin or disability.HOW TO APPLY & SELECTION PROCESS:Deadline for applications: 31/10/2026 (If no suitable candidate is found, the deadline will be extended)Number of positions available: 1Selection process:Pre-selection: Will be based on CV, motivation letter &experience.Interviews: Short-listed candidates will be interviewed.Job offer: Will be sent to the successful candidate after the interview.IRB BARCELONA endorses the Requirements and Principles of the European Charter for Researchers, the Code of Conduct for the Recruitment of Researchers, and Open, Transparent, Merit-based recruitment promoted by the European Commission and follows Equal Opportunities policies.On 9 December, 2014, IRB Barcelona was awarded the "HR Excellence in Research" logo. This recognition reflects the commitment of the Institute to the continuous improvement of its human resources policies in line with the Charter & Code. The Institute works to ensure fair and transparent recruitment and appraisal procedures.Please check our Recruitment Policy.Note: The strengths and weaknesses of the applications will be provided upon request.ABOUT IRB BARCELONA,Created in 2005 by the Generalitat de Catalunya (Government of Catalonia) and the University of Barcelona, IRB Barcelona is a Severo Ochoa Centre of Excellence—a seal that was awarded in 2011.The institute is devoted to conducting research of excellence in biomedicine and to transferring results to clinical practice, thus improving people’s quality of life, while simultaneously promoting the training of outstanding researchers, technology transfer, and public communication of science. Its 27 laboratories and 9 core facilities address basic questions in biology and are orientated to diseases such as cancer, metastasis, Alzheimer’s, diabetes, and rare conditions.IRB Barcelona is an international centre that hosts 500 members and 45 nationalities. It is located in the Barcelona Science Park. IRB Barcelona forms part of the Barcelona Institute of Science and Technology (BIST) and the “Xarxa de Centres de Recerca de Catalunya” (CERCA).#J-18808-Ljbffr

Concierge Physician position for a Royal Household in Doha with a tax-free package of £180,000 – £213,333. It requires full registration in the UK or Europe, 5+ years post-qualification clinical experience, and strict NDA compliance, with excellent English. Private accommodation, relocation support and comprehensive medical insurance are included. The QCHP licensing process is outlined before commitment; the appointment is madeby the Royal Household/appointing entity, with annual flights home #J-18808-Ljbffr

Somos un grupo de centros médicos especializados en el tratamiento integral del aparato locomotor, líder del sector rehabilitación del Barcelonès Nord. Con presencia en Badalona, Barcelona, Santa Coloma de Gramenet, El Masnou y Esplugues de Llobregat. Nacimos hace 40 años con el propósito de proporcionar asistencia médica de máxima calidad y asesoramiento en servicios de rehabilitación. Hemos atendido a más de 200.000 pacientes durante toda nuestra trayectoria. Nuestra esencia es el compromiso con nuestros pacientes y la mejora constante en nuestros procesos por tal de proporcionar la mejor calidad asistencial posible. Actualmente buscamos a un/a Médico/a Rehabilitador/a, quien será responsable de la evaluación, diagnóstico y tratamiento integral de pacientes con afecciones físicas, neuromusculares y funcionales, así como de la planificación y supervisión de programas de rehabilitación orientados a mejorar la calidad de vida y la funcionalidad de los pacientes. Asimismo, deberá trabajar de manera coordinada con un equipo multidisciplinario de profesionales de la salud. Requisitos Titulación de Medicina y Especialidad en Medicina Física y Rehabilitación (imprescindible ambos homologados). Habilitación profesional vigente para ejercer. Disponibilidad en Badalona y alrededores. Oferta Buen horario que facilita la conciliación entre vida personal y profesional. Retribución competitiva acorde con la experiencia y el perfil profesional. Entorno de trabajo estable, con oportunidades de desarrollo y crecimiento. Cultura organizativa orientada a la mejora continua y la excelencia asistencial. #J-18808-Ljbffr

JOB DESCRIPTION Neurologist specializing in movement disorders to conduct clinical research. MAIN RESPONSIBILITIES Participation in clinical trials at the Movement Disorders Unit, including conducting study visits, coordinating active research projects within the Unit, and monitoring patients. At the same time, training within the Movement Disorders Unit, providing support to the unit’s neurologists, as well as in the treatment and follow-up of patients with movement disorders undergoing advanced therapies such as deep brain stimulation and MRI-guided high-intensity focused ultrasound. QUALIFICATIONS AND EXPERIENCE Required level of education: Medical degree, Neurologist. Languages: Spanish, Catalan, English Personal skills: Knowledge of computer tools and database management. Required experience: Work experience in a specialized movement disorders unit will be taken into account, particularly prior experience with DBS and HIFU. WHAT WE OFFER Type of contract and working hours: Permanent, full-time employment contract under the Spanish Science Law / Ley de la Ciencia. Date of incorporation. 15/12/2026 Gross annual remuneration inherent to the square objected to this call, will be fixed based on the experience provided and the skills of the candidate, distributed in 12 payments. Flexible payment (childminding vouchers). 23 days holiday and 5 days for personal matters. Training capsules by the company. Be part of an excellent multidisciplinary research centre with the HRS4 R badge. Location on the Can Ruti Campus, a first-class translational research environment in the Barcelona area, in a very stimulating scientific environment. The IGTP offers a supportive, friendly and collaborative ecosystem to promote professional development and help you achieve your research goals. FOR MORE INFORMATION DEADLINE FOR APPLICATIONS The call for applications will close on October 26th, 2026 #J-18808-Ljbffr

Neurologist focused on movement disorders for clinical research, involving patient monitoring, trial participation, and advanced therapy support.

Pharmacists wanted to work in Community Pharmacy in the United KingdomWe are currently hiring community pharmacists to work in the following locations: Hereford, Lowestoft, Gillingham and Coleford.We need:Degree in Pharmacy by an EU University.Fluent English (C1/C2), ideally having passed the IELTS Academic or OET Pharmacy English language test.Training in pharmaceutical care will be welcomed.Experience in community pharmacy is welcomed but not mandatory.We offer:45 hours per week. Usually 9:00 to 18:00h Monday - Friday.Two year contract.Relocation package: up to 3000 € to cover various expenses.Various benefits and promotion opportunities.Visa paid by the employer and support to register as a Pharmacist in the UK.#J-18808-Ljbffr

Predoctoral Researcher sought for a 3D chromatin organization group focused on regulatory elements in hematological malignancies and cancer research.

¿Buscas trabajo en ayuda a la dependencia? Este mes de octubre surgen nuevas oportunidades para auxiliares de enfermería en Badalona. ¡Inscríbete gratis hoy mismo!

Plastic Surgeon – Wellness Kliniek Group Wellness Kliniek is growing! Are you a Plastic Surgeon with a love for aesthetic procedures? We have a job opening! Full‑time or part‑time. With over 25 years of experience and more than 150,000 satisfied patients, Wellness Kliniek is one of Europe's leading centers for cosmetic surgery. Our team strives every day to fulfill our mission: “More happy patients!”. You can find the list of procedures on our website As Plastic Surgeon, you work on an independent basis in an infrastructure provided by BIRAND SA. You are responsible for the medical process: your consultations, surgeries and the follow‑up of your patients. You will work according to ISO certified quality standards and protocols, in collaboration with a passionate team of experts in cosmetic surgery. Your responsibilities A cosmetic plastic surgeon at Wellness Kliniek is responsible for performing plastic surgery procedures; from consultations to follow‑up care, with the highest degree of safety and professionalism. Each surgeon provides ethical care, up‑to‑date knowledge, and collaboration with a medical team, for optimal patient outcomes. Along with the medical team, you guarantee continuity of care. This is you in a nutshell You are knowledgeable and experienced in aesthetic plastic surgery. You are registered as a plastic surgeon. You are language proficient, and preferably speak several languages. You highly value customer friendliness and friendly collegiality. A positive and professional attitude with a focus on quality and aesthetic results. What we offer You will work in a private clinic with a good reputation, with more than 150,000 satisfied patients. We have been operating for more than 25 years and guarantee quality care with an internationally recognized ISO Quality Label. Your work environment consists of an enthusiastic and driven team, within a modern clinic with secretarial support and skilled nurses. The medical team consists of national and international surgeons and anesthetists. The Wellness Kliniek in Genk, Belgium is managed by BIRAND NV, powered by Spronken Group, an established name in the healthcare sector best known for their quality, innovation and specialist expertise in cosmetic plastic surgery and orthopedic devices. If you are interested in this vacancy, please contact us. Your interest will be kept strictly confidential. We would like to invite you for a visit. Seniority level Executive Employment type Full‑time Job function Health Care Provider Industries Wellness and Fitness Services, Hospitals and Health Care, and Medical Practices #J-18808-Ljbffr

Get notified about new Pediatra jobs in Spain.Pamplona, Chartered Community of Navarre, Spain 1 month agoPamplona, Chartered Community of Navarre, Spain 2 months agoPSICOLOGO EXPERTO EN NEURODESARROLLO ROQUETAS DE MARGreater Barcelona Metropolitan Area 1 year agoPamplona, Chartered Community of Navarre, Spain Be an early applicant 1 week agoMETGES/SSES ESPECIALISTES MEDICINA FAMILIAR I COMUNITÀRIA CAP BARCELONETA (TELETREBALL 1 DIA SETMANAL)Colmenar Viejo, Community of Madrid, Spain Be an early applicant 5 hours agoMEDICO COLABORADOR (VARIAS ESPECIALIDADES)Madrid, Community of Madrid, Spain 1 week agoIbiza, Balearic Islands, Spain 1 month agoTres Cantos, Community of Madrid, Spain 3 days ago#J-18808-Ljbffr