Trabajos compliance en Burjassot - Page 6Crear alertas

&##127959;️ Shape the future of high-tech infrastructure at DAS Photonics. We're looking for a Facilities Manager to lead the technical design, implementation, and maintenance of our cutting-edge facilities, including the new cleanroom . As Facilities Manager, you will: Colaborate with the design, installation, and validation of critical infrastructure systems (HVAC, special gases, power supply). Coordinate contractors, suppliers, and validation bodies to ensure flawless execution. Ensure compliance and all applicable standards. Supervise preventive and corrective maintenance across equipment and systems. Lead a skilled technical team and guarantee operational excellence. Drive continuous improvement in energy efficiency, sustainability, and reliability . Support technical audits and collaborate with H&S and QA departments to ensure global compliance. This is a unique opportunity to lead the backbone of a world-class innovation ecosystem , working alongside brilliant engineers and scientists at the frontier of photonics and nanotechnology. &##128205; Location: Valencia, Spain &##128188; Type: Full-time &##127793; Environment: Innovation-driven, sustainable, and collaborative At DAS Photonics, we engineer the infrastructure of the future. &##127466;&##127480; &##127959;️ Diseña y lidera las infraestructuras del futuro en DAS Photonics. Buscamos un/a Responsable de Instalaciones para liderar el diseño técnico, la ejecución y el mantenimiento de nuestras instalaciones de alta tecnología, incluyendo la nueva sala blanca . Tus principales responsabilidades serán: Participar en el diseño y la implantación de las instalaciones y sistemas críticos (HVAC, climatización, gases especiales, suministro eléctrico). Coordinar contratistas, proveedores y organismos de validación, garantizando una ejecución excelente. Asegurar el cumplimiento de la normativas y demás regulaciones aplicables. Planificar y supervisar el mantenimiento preventivo y correctivo de equipos e infraestructuras. Liderar al equipo técnico de mantenimiento, garantizando fiabilidad y eficiencia operativa. Impulsar mejoras en eficiencia energética, sostenibilidad y disponibilidad técnica . Participar en auditorías y coordinar con PRL y QA el cumplimiento normativo global. Si te motiva trabajar en un entorno donde la ingeniería, la innovación y la precisión marcan la diferencia, esta es tu oportunidad para dejar huella en uno de los proyectos tecnológicos más relevantes del país. &##128205; Ubicación: Valencia, España &##128188; Tipo de puesto: Jornada completa &##127793; Entorno: Innovación, sostenibilidad y excelencia técnica En DAS Photonics diseñamos la infraestructura que impulsa la ciencia del mañana.

Company: Global Responsibility: Lead the assigned pharmaceutical formulation projects within the R&D department, planning, coordinating and supervising the activities of the projects assigned and report their progress to the R&D Manager, other departments and customers. Be responsible for formulation and process development activities associated with the pharmaceutical projects assigned. Develop the required document formulation and process development strategies for polymeric, biopolymeric, and hybrid drug delivery systems, particularly long-acting injectables (LAIs) and other controlled-release platforms. Analyze the status of patents that affect products under development and the results obtained in the clinical studies; coordinate, schedule, monitor, review and validate the proper sequence of the pharmaceutical development plan, batches for bioequivalence or clinical development and registration, reports and people involved, deciding, advising and reporting on the way forward in the development, deviations and modifications of pharmaceutical forms, according to SOP's, the ICH, EMEA and FDA guidance. Critically interpret analytical, preclinical, and clinical data to support development narratives, product characterization summaries, and manufacturing control justifications within the regulatory framework. Provide scientific rationale for biomaterial selection, formulation design, process parameters, and stability testing strategies in accordance with CMC principles. Ensure that the products and processes developed are suitable for a successful scale-up to commercial manufacturing. Interact with raw material vendors to select the suitable quality for API, excipients and container closure systems to be used for development and manufacturing. Plan, organize and coordinate the activities of pharmaceutical and analytical development to ensure the proper progress of the projects assigned. Design, direct and/or follow pre-formulation (compatibility studies), formulation development, process development, process optimization / scale-up on assigned projects. • Design and oversee the development of polymeric and biopolymeric formulations, ensuring reproducibility, scalability, and compliance with regulatory and industry standards., • electrospinning, electrospraying, emulsification), emphasizing data integrity and regulatory relevance for dossier inclusion or technology transfer., • Provide trouble shooting and optimization of formulations, process performance and technical performance in cooperation with the production department., • Prepare product development reports, write and review quality overall summary and other documents to support CMC regulatory submissions for filing and answering to deficiency letters., • Prepare the scientific documentation for quality and regulatory affairs to support the projects assigned and to meet the standard approval flow established by the quality system; all in accordance to GMP and CFR regulations, compliance with quality system and technical agreements and contracts with third parties so that projects progress properly., • Review and interpret results from analytical characterization (TGA, DSC, SEM, vibrational spectroscopy, mechanical testing, rheology, release profiles, etc.) Prepare summary reports and presentations for review by management., • Ensure good relationships and collaboration with all other teams involved in the development, QA, Patents, Medical, Regulatory Affairs, etc., • Ensure good relationships and efficient follow up and tracking of development activities outsourced to third party organizations. PhD in Pharmaceutical Sciences is a plus. • Fluent in English, basic knowledge of Spanish, knowledge of other languages will be an asset., • Experience (years/area): +5 years of experience in leading formulation R&D projects in the pharmaceutical sector. Experience in managing multiple projects and experience with FDA requirements desirable. • Impact and influence, good communication and project management skills, leadership., • Valid driver's license and own vehicle required.

Company: Global Responsibility: Lead the assigned pharmaceutical formulation projects within the R&D department, planning, coordinating and supervising the activities of the projects assigned and report their progress to the R&D Manager, other departments and customers. Be responsible for formulation and process development activities associated with the pharmaceutical projects assigned. Develop the required document formulation and process development strategies for polymeric, biopolymeric, and hybrid drug delivery systems, particularly long-acting injectables (LAIs) and other controlled-release platforms. Analyze the status of patents that affect products under development and the results obtained in the clinical studies; coordinate, schedule, monitor, review and validate the proper sequence of the pharmaceutical development plan, batches for bioequivalence or clinical development and registration, reports and people involved, deciding, advising and reporting on the way forward in the development, deviations and modifications of pharmaceutical forms, according to SOP's, the ICH, EMEA and FDA guidance. Critically interpret analytical, preclinical, and clinical data to support development narratives, product characterization summaries, and manufacturing control justifications within the regulatory framework. Provide scientific rationale for biomaterial selection, formulation design, process parameters, and stability testing strategies in accordance with CMC principles. Ensure that the products and processes developed are suitable for a successful scale-up to commercial manufacturing. Interact with raw material vendors to select the suitable quality for API, excipients and container closure systems to be used for development and manufacturing. Plan, organize and coordinate the activities of pharmaceutical and analytical development to ensure the proper progress of the projects assigned. Design, direct and/or follow pre-formulation (compatibility studies), formulation development, process development, process optimization / scale-up on assigned projects. • Design and oversee the development of polymeric and biopolymeric formulations, ensuring reproducibility, scalability, and compliance with regulatory and industry standards., • electrospinning, electrospraying, emulsification), emphasizing data integrity and regulatory relevance for dossier inclusion or technology transfer., • Provide trouble shooting and optimization of formulations, process performance and technical performance in cooperation with the production department., • Prepare product development reports, write and review quality overall summary and other documents to support CMC regulatory submissions for filing and answering to deficiency letters., • Prepare the scientific documentation for quality and regulatory affairs to support the projects assigned and to meet the standard approval flow established by the quality system; all in accordance to GMP and CFR regulations, compliance with quality system and technical agreements and contracts with third parties so that projects progress properly., • Review and interpret results from analytical characterization (TGA, DSC, SEM, vibrational spectroscopy, mechanical testing, rheology, release profiles, etc.) Prepare summary reports and presentations for review by management., • Ensure good relationships and collaboration with all other teams involved in the development, QA, Patents, Medical, Regulatory Affairs, etc., • Ensure good relationships and efficient follow up and tracking of development activities outsourced to third party organizations. PhD in Pharmaceutical Sciences is a plus. • Fluent in English, basic knowledge of Spanish, knowledge of other languages will be an asset., • Experience (years/area): +5 years of experience in leading formulation R&D projects in the pharmaceutical sector. Experience in managing multiple projects and experience with FDA requirements desirable. • Impact and influence, good communication and project management skills, leadership., • Valid driver's license and own vehicle required.

Company: Global Responsibility: Lead the assigned pharmaceutical formulation projects within the R&D department, planning, coordinating and supervising the activities of the projects assigned and report their progress to the R&D Manager, other departments and customers. Be responsible for formulation and process development activities associated with the pharmaceutical projects assigned. Develop the required document formulation and process development strategies for polymeric, biopolymeric, and hybrid drug delivery systems, particularly long-acting injectables (LAIs) and other controlled-release platforms. Analyze the status of patents that affect products under development and the results obtained in the clinical studies; coordinate, schedule, monitor, review and validate the proper sequence of the pharmaceutical development plan, batches for bioequivalence or clinical development and registration, reports and people involved, deciding, advising and reporting on the way forward in the development, deviations and modifications of pharmaceutical forms, according to SOP's, the ICH, EMEA and FDA guidance. Critically interpret analytical, preclinical, and clinical data to support development narratives, product characterization summaries, and manufacturing control justifications within the regulatory framework. Provide scientific rationale for biomaterial selection, formulation design, process parameters, and stability testing strategies in accordance with CMC principles. Ensure that the products and processes developed are suitable for a successful scale-up to commercial manufacturing. Interact with raw material vendors to select the suitable quality for API, excipients and container closure systems to be used for development and manufacturing. Plan, organize and coordinate the activities of pharmaceutical and analytical development to ensure the proper progress of the projects assigned. Design, direct and/or follow pre-formulation (compatibility studies), formulation development, process development, process optimization / scale-up on assigned projects. • Design and oversee the development of polymeric and biopolymeric formulations, ensuring reproducibility, scalability, and compliance with regulatory and industry standards., • electrospinning, electrospraying, emulsification), emphasizing data integrity and regulatory relevance for dossier inclusion or technology transfer., • Provide trouble shooting and optimization of formulations, process performance and technical performance in cooperation with the production department., • Prepare product development reports, write and review quality overall summary and other documents to support CMC regulatory submissions for filing and answering to deficiency letters., • Prepare the scientific documentation for quality and regulatory affairs to support the projects assigned and to meet the standard approval flow established by the quality system; all in accordance to GMP and CFR regulations, compliance with quality system and technical agreements and contracts with third parties so that projects progress properly., • Review and interpret results from analytical characterization (TGA, DSC, SEM, vibrational spectroscopy, mechanical testing, rheology, release profiles, etc.) Prepare summary reports and presentations for review by management., • Ensure good relationships and collaboration with all other teams involved in the development, QA, Patents, Medical, Regulatory Affairs, etc., • Ensure good relationships and efficient follow up and tracking of development activities outsourced to third party organizations. PhD in Pharmaceutical Sciences is a plus. • Fluent in English, basic knowledge of Spanish, knowledge of other languages will be an asset., • Experience (years/area): +5 years of experience in leading formulation R&D projects in the pharmaceutical sector. Experience in managing multiple projects and experience with FDA requirements desirable. • Impact and influence, good communication and project management skills, leadership., • Valid driver's license and own vehicle required.

Company: Global Responsibility: Lead the assigned pharmaceutical formulation projects within the R&D department, planning, coordinating and supervising the activities of the projects assigned and report their progress to the R&D Manager, other departments and customers. Be responsible for formulation and process development activities associated with the pharmaceutical projects assigned. Develop the required document formulation and process development strategies for polymeric, biopolymeric, and hybrid drug delivery systems, particularly long-acting injectables (LAIs) and other controlled-release platforms. Analyze the status of patents that affect products under development and the results obtained in the clinical studies; coordinate, schedule, monitor, review and validate the proper sequence of the pharmaceutical development plan, batches for bioequivalence or clinical development and registration, reports and people involved, deciding, advising and reporting on the way forward in the development, deviations and modifications of pharmaceutical forms, according to SOP's, the ICH, EMEA and FDA guidance. Critically interpret analytical, preclinical, and clinical data to support development narratives, product characterization summaries, and manufacturing control justifications within the regulatory framework. Provide scientific rationale for biomaterial selection, formulation design, process parameters, and stability testing strategies in accordance with CMC principles. Ensure that the products and processes developed are suitable for a successful scale-up to commercial manufacturing. Interact with raw material vendors to select the suitable quality for API, excipients and container closure systems to be used for development and manufacturing. Plan, organize and coordinate the activities of pharmaceutical and analytical development to ensure the proper progress of the projects assigned. Design, direct and/or follow pre-formulation (compatibility studies), formulation development, process development, process optimization / scale-up on assigned projects. • Design and oversee the development of polymeric and biopolymeric formulations, ensuring reproducibility, scalability, and compliance with regulatory and industry standards., • electrospinning, electrospraying, emulsification), emphasizing data integrity and regulatory relevance for dossier inclusion or technology transfer., • Provide trouble shooting and optimization of formulations, process performance and technical performance in cooperation with the production department., • Prepare product development reports, write and review quality overall summary and other documents to support CMC regulatory submissions for filing and answering to deficiency letters., • Prepare the scientific documentation for quality and regulatory affairs to support the projects assigned and to meet the standard approval flow established by the quality system; all in accordance to GMP and CFR regulations, compliance with quality system and technical agreements and contracts with third parties so that projects progress properly., • Review and interpret results from analytical characterization (TGA, DSC, SEM, vibrational spectroscopy, mechanical testing, rheology, release profiles, etc.) Prepare summary reports and presentations for review by management., • Ensure good relationships and collaboration with all other teams involved in the development, QA, Patents, Medical, Regulatory Affairs, etc., • Ensure good relationships and efficient follow up and tracking of development activities outsourced to third party organizations. PhD in Pharmaceutical Sciences is a plus. • Fluent in English, basic knowledge of Spanish, knowledge of other languages will be an asset., • Experience (years/area): +5 years of experience in leading formulation R&D projects in the pharmaceutical sector. Experience in managing multiple projects and experience with FDA requirements desirable. • Impact and influence, good communication and project management skills, leadership., • Valid driver's license and own vehicle required.

Are you a skilled Clinical Trial Statistician eager to contribute your expertise to advancing women's health? Do you want to apply your statistical knowledge to the design, analysis, and interpretation of clinical trials that could improve the quality of life and reproductive health of women worldwide? At the Carlos Simon Foundation, we are at the forefront of research in reproductive medicine and women's health, and we are looking for talented professionals to join our multidisciplinary team. As a Clinical Trial Statistician at the Carlos Simon Foundation, you will play a pivotal role in shaping the statistical design of clinical studies, developing analysis strategies, ensuring compliance with international regulatory standards, and providing expert guidance to multidisciplinary teams. Your work will directly impact the scientific rigor and clinical relevance of our trials, supporting our mission to remove barriers to women's health and reproductive desire. Statistical Design of the Clinical Trial Define analysis strategies to evaluate the efficacy and safety of the treatment/medical device. Preparation of the Statistical Analysis Plan (SAP) Write the Statistical Analysis Plan (SAP) detailing all the statistical methodologies to be used. Coordinate the review and approval of the SAP with other clinical and technical teams involved. Ensure that the SAP complies with regulatory regulations (FDA, EMA). Statistical Analysis of Clinical Data Perform descriptive and inferential analyses to evaluate clinical trial results. Apply appropriate statistical tests (ANOVA, regression, survival models, etc.). Generate tables, graphs, and lists according to SAP. Evaluate the consistency and validity of the data through quality controls. Coding and Analysis of Adverse Events (MedDRA) Apply MedDRA for coding adverse events and medical terms in the study. Validate the correct classification of adverse events and their impact on safety analysis. Coordinate with physicians and pharmacovigilance to ensure consistency in coding. Contribute to the preparation of the Clinical Study Report (CSR) integrating statistical analysis. Ensure that analyses comply with Good Clinical Practice (GCP) regulations. Document processes to ensure reproducibility and transparency of analysis. Advice on Data Interpretation and Decision Making: Provide expert advice on the results of statistical analyses to facilitate decision-making within multidisciplinary teams (medical, scientific, regulatory, etc.). Propose adjustments or redesigns in statistical analyses as studies progress, considering preliminary results and the context of the clinical trial. To perform Interim Analysis if applicable. University degree in Statistics, Mathematics, Biostatistics, or related. A PhD or a comparable work experience in statistics applied to clinical trials. Minimum 3 years of experience in statistics applied to clinical trials, with practical experience in managing several projects. Verifiable experience in the development of SAP, statistical final reports and CSRs in clinical trials. Management of adverse event coding using MedDRA and knowledge of other classifications such as CTCAE. Mastery of statistical tools such as SAS, R, SPSS or other programs used in the pharmaceutical industry. In-depth knowledge of experimental design, multivariate analysis and advanced statistical techniques. Experience or Knowledge in clinical trials with Bayesian design will be valued. Experience in validating data and executing data quality controls. Excellent project management, organization, task prioritization, and technical report writing skills. Ability to work under pressure and manage multiple projects simultaneously. Attention to detail and rigor in data validation. Flexible working hours and hybrid work mode. ~ Internal training opportunities and a collaborative research environment. ~ Access to flexible compensation program (meal, nursery, transport vouchers, health insurance). ~ On-site childcare program during school holidays. ~ Free coffee, snacks and kitchen essentials. ~ Team events: summer dinner, holiday celebration, paella contest.

Are you ready to make a significant contribution to both saving lives and protecting communities? At Avincis, we're dedicated to meaningful work with a clear purpose. We're seeking talented individuals passionate about making a difference while growing their careers in a dynamic environment. Avincis is one of the world's leading Emergency Aerial Service Operators and the largest in Europe. We operate from more than 180 bases across Spain, Portugal, Italy, Norway, Sweden, Finland, Greece, Mozambique and Chile. We operate a fleet of approximately 205 aircraft which includes 165 helicopters and 40 aeroplanes. Join us and be part of a mission to protect lives, safeguard communities, and make a positive impact. The Head of Applications will be responsible for leading the strategy, management, and evolution of corporate third-party applications — including core systems such as SAP and aviation software like Air Maestro or Gannet — ensuring alignment with business needs and the company's strategic objectives. Reporting to the Group Chief Information Officer, this role also oversees and coordinates the team of IT Business Partners, who act as the main interface between IT and the business, ensuring proper demand management, requirements gathering, and functional analysis to deliver effective and scalable technology solutions. The selected person may be based in any of our offices located in Spain, Italy, Portugal, Sweden, or Norway . Main responsabilities Third-Party Applications Management: • Leads the strategy, governance, and operation of corporate applications (SAP, Finance, HR, Supply Chain, etc.)., • Manages vendor relationships, including contractual, budgetary, and service delivery aspects., • Oversees the full lifecycle of applications: maintenance, upgrades, licensing, and roadmap definition., • Leads and develops the IT Business Partners team, ensuring they act as the primary contact point between IT and business units., • Ensures high-quality functional documentation and requirements analysis., • Drives the identification of improvement and digitization opportunities in close collaboration with business areas., • Contributes to the overall IT strategy definition alongside the CIO and the IT leadership team., • Ensures technology solutions are aligned with corporate objectives., • In-depth functional knowledge and experience in SAP and other key third-party business applications., • Experience in demand management and functional documentation, with proven ability to manage and track projects and tasks using platforms such as Azure DevOps, Jira, Asana or similar., • Strong leadership and team management skills., • Excellent communication and negotiation abilities with both business stakeholders and vendors., • Results-oriented, with the ability to prioritise effectively in high-demand and dynamic environments., • Strategic mindset combined with a focus on continuous improvement and innovation., • Proficient in problem-solving, and able to navigate complex data environments with autonomy., • Minimum of 8–10 years' experience in IT roles related to enterprise applications, with at least 3 years in a management role., • Proven experience managing enterprise applications (ERP, SAP, CRM, HR systems, etc.)., • Strong track record in vendor management, including contracts and budgets. As the aviation sector is highly regulated, safety and compliance are the highest priority. Avincis is also committed to the highest standards of business ethics with integrity with trust being central values of the organisation. Every employee in Avincis is expected to be a role model of integrity and high ethical standards. Our culture is grounded in a shared commitment to excellence, collaboration, and respect. We believe that how we work is just as important as what we achieve. Our six core values guide our actions and define who we are: • Safety : We uphold safety as our first priority above all other business outcomes., • Integrity: We are honest, do the right thing, and communicate respectfully and appropriately., • Trust : We foster an environment of openness and reliability, where trust is earned and valued., • Teamwork: We work together and collaborate to achieve collective goals, ensuring that everyone feels welcome in an inclusive and diverse workplace., • Respect : We treat all employees, customers, and stakeholders with dignity, courtesy, and kindness. We listen to others' ideas and welcome their input to improve. Note: As a company committed to equal opportunities between women and men, AVINCIS evaluates all applications according to objective criteria in order to select the most suitable person for the position offered, regardless of gender. In accordance with the provisions of Regulation (EU) 2016/679 of 27 April 2016 (RGPD) and Organic Law 3/2018, of 5 December, on Data Protection and Guarantee of Digital Rights, we inform you and request your consent, or that of your legal representative, to incorporate your data into the files of AVINCIS, as data controller, and to process them in order to carry out your selection process and maintain a comprehensive relationship with you. The NIF of the Data Controller is A-03125010 and the address is Aeródromo de Mutxamel, Partida la Almaina, nº92, CP: 03110, Mutxamel, Alicante. In this act you give your consent to the transfer of your data, present and future, to those companies and professionals who need your services for the proper completion of the order made by the Data Controller. You may exercise your rights of access, rectification, cancellation and opposition in the manner and in accordance with the procedures established in the aforementioned Organic Law, by writing to the above address or to the e-mail address . The owner of the data is responsible, in any case, for the truthfulness, accuracy, validity, authenticity and relevance of the Personal Data provided. AVINCIS will only use the information provided by you for the selection process in which you are involved, or others in which you could be a candidate, unless otherwise indicated, and the signatories undertake to maintain the strictest confidentiality regarding the information obtained inthis process.

&##127959;️ Shape the future of high-tech infrastructure at DAS Photonics. We're looking for a Facilities Manager to lead the technical design, implementation, and maintenance of our cutting-edge facilities, including the new cleanroom . As Facilities Manager, you will: Colaborate with the design, installation, and validation of critical infrastructure systems (HVAC, special gases, power supply). Coordinate contractors, suppliers, and validation bodies to ensure flawless execution. Ensure compliance and all applicable standards. Supervise preventive and corrective maintenance across equipment and systems. Lead a skilled technical team and guarantee operational excellence. Drive continuous improvement in energy efficiency, sustainability, and reliability . Support technical audits and collaborate with H&S and QA departments to ensure global compliance. This is a unique opportunity to lead the backbone of a world-class innovation ecosystem , working alongside brilliant engineers and scientists at the frontier of photonics and nanotechnology. &##128205; Location: Valencia, Spain &##128188; Type: Full-time &##127793; Environment: Innovation-driven, sustainable, and collaborative At DAS Photonics, we engineer the infrastructure of the future. &##127466;&##127480; &##127959;️ Diseña y lidera las infraestructuras del futuro en DAS Photonics. Buscamos un/a Responsable de Instalaciones para liderar el diseño técnico, la ejecución y el mantenimiento de nuestras instalaciones de alta tecnología, incluyendo la nueva sala blanca . Tus principales responsabilidades serán: Participar en el diseño y la implantación de las instalaciones y sistemas críticos (HVAC, climatización, gases especiales, suministro eléctrico). Coordinar contratistas, proveedores y organismos de validación, garantizando una ejecución excelente. Asegurar el cumplimiento de la normativas y demás regulaciones aplicables. Planificar y supervisar el mantenimiento preventivo y correctivo de equipos e infraestructuras. Liderar al equipo técnico de mantenimiento, garantizando fiabilidad y eficiencia operativa. Impulsar mejoras en eficiencia energética, sostenibilidad y disponibilidad técnica . Participar en auditorías y coordinar con PRL y QA el cumplimiento normativo global. Si te motiva trabajar en un entorno donde la ingeniería, la innovación y la precisión marcan la diferencia, esta es tu oportunidad para dejar huella en uno de los proyectos tecnológicos más relevantes del país. &##128205; Ubicación: Valencia, España &##128188; Tipo de puesto: Jornada completa &##127793; Entorno: Innovación, sostenibilidad y excelencia técnica En DAS Photonics diseñamos la infraestructura que impulsa la ciencia del mañana.

Spanish-speaking Content Reviewer.In this role, you’ll play a key part in reviewing and handling.From privacy claims and fraud to defamation and falsification, you’ll be on the front line of.On-site or Remote (only within Greece).Monitor digital activity and ensure compliance with platform.

AML Specialist needed for a hybrid role in Madrid, Spain.Responsibilities include compliance matters, KYC transactions analysis, and AML procedures.

About Revolut People deserve more from their money.More visibility, more control, and more freedom.Since 2015, Revolut has been on a mission to deliver just that.Our powerhouse of products — including spending, saving, investing, exchanging, travelling, and more — help our 60+ million customers

Manages HR, ensuring compliance with labor laws, coordinating with teams, and leading a team of two.

Qué te ofrecemos?Más allá del alcance de tu proyecto directo, formarás parte de la práctica Finance, Risk and Compliance para el sector Bancario, en la que te encontrarás con un equipo dinámico, joven, entusiasta y siempre orientado hacia el éxito, a partir de una fuerte cultura emprendedora

Oversee financial controls, reporting, and compliance for Spain and the UK, bridging operations and shared services.

Lead Legal and Compliance, set strategy, and partner with senior leadership on M&A and corporate matters.

Lead cybersecurity strategy and drive security transformation, including risk assessments and compliance.

The person in this role will identify opportunities to improve existing vendor management practices, optimize cost structures, maximize margins, and ensure that linguistic quality consistently meets our high standards. Ensure vendor compliance with company standards, NDAs, confidentiality requiremen

Manages configuration of GNSS projects, ensuring compliance and supporting project delivery, including documentation, and hardware integration.

Safety Engineer needed to perform risk analysis, define safety concepts, and ensure compliance with safety standards for robotics and industrial equipment.