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🔹 We're Hiring: Full-Time Dentist at CeraRoot CLINIC (Barcelona) 🔹 CeraRoot CLINIC is expanding! We’re looking for a motivated and skilled full-time dentist to join our multidisciplinary team in Barcelona, where innovation meets clinical excellence. 🦷 About the Role As part of our clinical team, you’ll be responsible for: • Treating patients with a biological and holistic approach, • Designing and planning treatments using CAD/CAM digital workflows, • Collaborating with our Quality Department to ensure compliance 🌱 What We Offer • Full-time contract, • Structured training and career development, • A dynamic work environment at the forefront of digital technology and ceramic implantology, • Opportunity to grow within an internationally recognized company ✅ Requirements • Degree in Dentistry, • Ideally a smart young dentist with Interest to grow in multiple areas of dentistry, including digital dentistry, cad/cam design and production, ceramic implantology and metal-free dentistry, • Comfortable with technology and digital dentistry, • Team player with a patient-centered mindset, • English and Spanish (working proficiency) 📍Location: CeraRoot CLINIC – Les Franqueses del Valles , Barcelona, Spain 🕒 Start date: As soon as possible Interested or know someone who might be a great fit? 👉 Apply now or message us directly for more details! #Dentist #HiringDentist #DentalJobs #BarcelonaJobs #CeraRoot #BiologicalDentistry #CADCAM #CeramicImplants #FullTimeJob

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia, and the Americas. About the Role Due to our constant growth, we are looking for a Project Engineer - Pharmaceutical and Packaging Projects to support our projects in Parets del Vallès, Catalonia, Spain. Responsibilities • Managing the planning, execution, and successful completion of pharmaceutical and packaging projects., • Coordinating with cross-functional teams to ensure project timelines and objectives are achieved., • Supervising installation and commissioning of pharmaceutical and packaging equipment., • Conducting maintenance and troubleshooting activities to maintain optimal system performance., • Providing technical support and training to on-site personnel., • Ensuring strict compliance with industry standards and regulatory requirements., • Preparing detailed reports and documentation regarding project progress and equipment performance. Qualifications • Bachelor's degree in Engineering (Mechanical, Electrical, or Industrial)., • Minimum of 3 years' experience in the pharmaceutical and packaging industries., • Solid knowledge of pharmaceutical manufacturing and packaging processes and equipment., • Strong project management skills and high attention to detail., • Excellent communication and interpersonal skills., • Ability to work both independently and collaboratively., • Willingness to travel to various project sites as needed. Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome from the Hiring Manager interview, the recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills, and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Desde ManpowerGroup Talent Solutions estamos buscando un Experto en implementaciones desde cero de LIMS, para una empresa multinacional del sector pharma, referente en medicamentos genéricos de valor añadido, ubicada en Martorelles. Dentro del departamento de IT Quality and Compliance, tus funciones principales serán: • Implementar un sistema LIMS desde cero para gestionar integralmente los laboratorios de Control de Calidad e I+D, eliminando por completo el uso de papel., • Diseñar y desarrollar una arquitectura modular que permita la integración escalonada de los diferentes módulos del LIMS, garantizando flexibilidad y adaptabilidad a las necesidades del negocio., • Automatizar la captura de datos conectando equipos e instrumentos de laboratorio al LIMS para mejorar la trazabilidad, minimizar errores y optimizar la eficiencia operativa., • Implementar un Sistema de Ejecución de Laboratorio (LES) que digitalice los flujos de trabajo del laboratorio, incluyendo la gestión de muestras, reactivos, análisis e informes., • Implementar un cuaderno electrónico de laboratorio (ELN) en el área de I+D, facilitando la documentación estructurada y el cumplimiento normativo de la investigación., • Garantizar la integración del LIMS con otros sistemas corporativos (ERP, MES, sistemas de calidad, etc.) para lograr una gestión eficiente y centralizada de la información., • Responsable de supervisar el mantenimiento de la aplicación LIMS, optimizando las nuevas funcionalidades como herramientas de IA. Trabajar en un entorno regulado, garantizando el cumplimiento de las normativas aplicables al sector farmacéutico, como GMP, FDA 21 CFR Parte 11, GAMP 5 e ISO., • Colaborar en la validación del sistema LIMS, siguiendo las mejores prácticas de Validación de Sistemas Informáticos (CSV) para garantizar el cumplimiento de los requisitos normativos., • Gestionar la seguridad y la accesibilidad de los datos, estableciendo los controles y permisos adecuados., • Capacitar a los usuarios y gestionar la adopción del sistema, asegurándose de que los equipos de laboratorio estén familiarizados con el LIMS y sus funcionalidades., • Colaborar estrechamente con equipos multidisciplinares (TI, Calidad, Producción, I+D, proveedores) para garantizar el éxito del proyecto. Requisitos: • Mínimo 3 años como Consultor o Técnico LIMS., • Sistemas LIMS. Configuración o programación de estos sistemas., • Empower, LabX, LIMS (distintos fabricantes)., • Inglés nivel B2 a nivel comprensión, • Se valorará la experiencia en el cumplimiento de regulaciones de la industria farmacéutica como GMP, FDA 21 CFR Parte 11, GAMP 5 e ISO., • Project Management Methodology. Competencias: • Liderazgo y mentalidad orientada a resultados, • Trabajo en equipo y comunicación efectiva, • Adaptabilidad y gestión del cambio, • Resolución de problemas y proactividad, • Atención al detalle, • Autonomía y toma de decisiones, • Compromiso y responsabilidad Qué te ofrecemos: • Entorno de trabajo que promueve el aprendizaje y desarrollo., • Contrato indefinido directamente con cliente, • Modelo de trabajo híbrido (3 días de teletrabajo a la semana, con flexibilidad si hay que acudir algún día extra, de forma esporádica), • Seguro de vida y accidentes, • Retribución Flexible (Seguro Médico, Ticket Restaurant, Tarjeta Transporte, Guardería y Formación), • E-Learning (Acceso a una plataforma de E-learning gratuita con más de 100 cursos, • Idiomas: Clases en Plataforma Online Gratuita, • Flexibilidad Horaria, de vacaciones y teletrabajo, • Horario: Lunes a Jueves flexibilidad 7:00-9:30h. Salida a partir de las 16:00h en adelante. Viernes a partir de les 15:30h, • Cantina 4 euros al menú. En los procesos de selección garantizamos la igualdad de oportunidades. Trabajamos para crear equipos diversos y estamos convencidos de que una cultura y un entorno inclusivos nos ayudan a hacer realidad nuestro propósito: mejorar la vida de las personas, empezando por nosotros mismos

PHILIPP PLEIN is a highly successful luxury fashion brand. The driving force behind the company is human inspiration and creativity, with the goal of setting trends rather than following them. This strong belief has paved the way for the brand to become the international lifestyle label it is today. All our collections can be seen as works of art and are synonymous with nobility and perfection. Our daily challenge is always to live up to the expectations of our customers around the world. Duties and Responsibilities: • Leadership and Team Management:, • Recruit, train, and supervise store staff, including sales associates, cashiers, and stockroom personnel., • Provide guidance, coaching, and performance feedback to maximize employee productivity and job satisfaction., • Foster a positive work environment that encourages teamwork, professionalism, and exceptional customer service., • Set clear expectations and goals for the team and motivate them to achieve targets. Sales and Customer Service: • Develop and execute sales strategies to drive revenue growth and meet or exceed sales targets., • Monitor and analyse sales figures, identify trends, and implement necessary measures to optimize sales performance., • Ensure excellent customer service standards are maintained at all times, resolving customer issues and inquiries in a timely and satisfactory manner., • Build and maintain strong customer relationships, ensuring customer loyalty and repeat business. Store Operations and Merchandising: • Oversee the day-to-day operations of the store, including opening and closing procedures, cash management, and inventory control., • Ensure the store is clean, organized, and well-maintained to provide an inviting shopping environment., • Implement effective visual merchandising techniques to enhance product presentation and maximize sales opportunities., • Monitor and manage inventory levels, replenishment, and product ordering to avoid stockouts and minimize overstock situations. Financial Management: • Develop and manage the store's budget, including sales forecasts, expense control, and profitability analysis., • Monitor key performance indicators (KPIs) such as sales, gross margin, and labor costs to drive financial success., • Analyze financial reports, identify areas for improvement, and implement corrective actions as needed., • Control operational costs and minimize wastage to maximize profitability. Safety and Compliance: • Ensure compliance with all company policies, procedures, and legal regulations., • Maintain a safe working environment for employees and customers, following health and safety guidelines., • Stay updated with industry trends, market conditions, and competitors' activities to adapt strategies accordingly. Profile: • Proven experience as a Store Manager or in a similar role., • Strong leadership and people management skills., • Excellent communication and interpersonal abilities., • Sound knowledge of retail operations and merchandising techniques., • Proficient in analysing sales data and financial reports., • Ability to work under pressure and make effective decisions., • Familiarity with point-of-sale (POS) systems and inventory management software., • Flexibility to work evenings, weekends, and holidays as required., • Possibility of a permanent contract that will be evaluated with the candidate during the job interview. We are looking for a highly motivated individual who can represent our brand with enthusiasm and professionalism. The ideal candidate has experience driving CRM initiatives, strong attention to detail, and a results-oriented mindset. They possess a positive attitude and a genuine passion for the fashion industry. Send your cv:

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia, and the Americas. About the Role Due to our constant growth, we are looking for a Project Engineer - Pharmaceutical and Packaging Projects to support our projects in Parets del Vallès, Catalonia, Spain. Responsibilities • Managing the planning, execution, and successful completion of pharmaceutical and packaging projects., • Coordinating with cross-functional teams to ensure project timelines and objectives are achieved., • Supervising installation and commissioning of pharmaceutical and packaging equipment., • Conducting maintenance and troubleshooting activities to maintain optimal system performance., • Providing technical support and training to on-site personnel., • Ensuring strict compliance with industry standards and regulatory requirements., • Preparing detailed reports and documentation regarding project progress and equipment performance. Qualifications • Bachelor's degree in Engineering (Mechanical, Electrical, or Industrial)., • Minimum of 3 years' experience in the pharmaceutical and packaging industries., • Solid knowledge of pharmaceutical manufacturing and packaging processes and equipment., • Strong project management skills and high attention to detail., • Excellent communication and interpersonal skills., • Ability to work both independently and collaboratively., • Willingness to travel to various project sites as needed. Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome from the Hiring Manager interview, the recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills, and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia, and the Americas. About the Role Due to our constant growth, we are looking for a Project Engineer - Pharmaceutical and Packaging Projects to support our projects in Parets del Vallès, Catalonia, Spain. Responsibilities • Managing the planning, execution, and successful completion of pharmaceutical and packaging projects., • Coordinating with cross-functional teams to ensure project timelines and objectives are achieved., • Supervising installation and commissioning of pharmaceutical and packaging equipment., • Conducting maintenance and troubleshooting activities to maintain optimal system performance., • Providing technical support and training to on-site personnel., • Ensuring strict compliance with industry standards and regulatory requirements., • Preparing detailed reports and documentation regarding project progress and equipment performance. Qualifications • Bachelor's degree in Engineering (Mechanical, Electrical, or Industrial)., • Minimum of 3 years' experience in the pharmaceutical and packaging industries., • Solid knowledge of pharmaceutical manufacturing and packaging processes and equipment., • Strong project management skills and high attention to detail., • Excellent communication and interpersonal skills., • Ability to work both independently and collaboratively., • Willingness to travel to various project sites as needed. Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome from the Hiring Manager interview, the recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills, and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Ensure compliance with all company policies, procedures, and legal regulations. Proven experience as a Store Manager or in a similar role. This strong belief has paved the way for the brand to become the international lifestyle label it is today.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia, and the Americas. About the Role Due to our constant growth, we are looking for a Project Engineer - Pharmaceutical and Packaging Projects to support our projects in Parets del Vallès, Catalonia, Spain. Responsibilities • Managing the planning, execution, and successful completion of pharmaceutical and packaging projects., • Coordinating with cross-functional teams to ensure project timelines and objectives are achieved., • Supervising installation and commissioning of pharmaceutical and packaging equipment., • Conducting maintenance and troubleshooting activities to maintain optimal system performance., • Providing technical support and training to on-site personnel., • Ensuring strict compliance with industry standards and regulatory requirements., • Preparing detailed reports and documentation regarding project progress and equipment performance. Qualifications • Bachelor's degree in Engineering (Mechanical, Electrical, or Industrial)., • Minimum of 3 years' experience in the pharmaceutical and packaging industries., • Solid knowledge of pharmaceutical manufacturing and packaging processes and equipment., • Strong project management skills and high attention to detail., • Excellent communication and interpersonal skills., • Ability to work both independently and collaboratively., • Willingness to travel to various project sites as needed. Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome from the Hiring Manager interview, the recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills, and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Immunoassay business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Within a medical device environment, work with the QARA Manager to ensure regulatory compliance and certification of software products. Key Accountabilities Be a key part of a team where you will: • Collaborate in maintaining the quality system documentation processes and procedures adopted by the company., • Investigate and resolve quality issues, implementing corrective and preventive actions to mitigate recurrence., • Coordinate and support the preparation of software technical documents appropriate for regulatory submissions., • Support the regulatory submissions for market authorization for medical device products., • Conduct internal assessments and audits to identify areas for improvement and ensure adherence to established procedures., • Facilitate the approval process for software releases., • Disseminating knowledge about the Quality System and regulatory requirements., • Review Promotional and advertising materials., • Oversee post-market surveillance activities related to medical device products., • Offer guidance and mentorship to QARA team members at lower levels Networking/Key relationships The main relationships within to the Werfen Group are: • QARA Manger, QA Leads, Validation Led, • Factory Lead and Solution Leaders, • Customer, • Application Lifecycle manager (ALM), • Notified Bodies and Competent Authorities for product regulatory compliance., • This position may also require also cooperating with other companies inside Werfen. Minimum Knowledge & Experience required for the position: • Engineer, computer Science or other Technical carrier, or equivalent work experience., • A minimum of 5 years experience in Quality Assurance or Regulatory related, preferably within the Healthcare sector, • Additional Skills/Knowledge:, • Knowledge and experience working with medical device international regulations and related standards (ISO 13485, ISO 14971,..)., • Knowledge and experience working in Medical device software life cycle process (IEC 62304), • Desirable:, • Knowledge and experience working in medical device regulatory submissions (MDR/IVDR,FDA..), • Internal auditor qualification for management systems or knowledge of auditing techniques Skills & Capabilities: The ideal candidate for this position will exhibit the following skills and competencies: • Good level of Technical and Conversional English., • Team player with ability to work independently., • Excellent and effective written and verbal communication skills., • Excellent interpersonal skills, good judgment and analytical skills., • Effective time management and organizational skills What we offer: • A meaningful project that will impact the quality of laboratory software medicine worldwide, • 3 days a week working from home, • Multicultural and friendly team, • Exciting opportunities for professional development., • Ongoing training, • Social benefits: Canteen, nursery check, English training..., • All the benefits according to the chemical agreement Our Purpose: We contribute to the advancement of patient care around the world through innovative specialized diagnostics JOIN US!

PHILIPP PLEIN is a highly successful luxury fashion brand. The driving force behind the company is human inspiration and creativity, with the goal of setting trends rather than following them. This strong belief has paved the way for the brand to become the international lifestyle label it is today. All our collections can be seen as works of art and are synonymous with nobility and perfection. Our daily challenge is always to live up to the expectations of our customers around the world. Duties and Responsibilities: • Leadership and Team Management:, • Recruit, train, and supervise store staff, including sales associates, cashiers, and stockroom personnel., • Provide guidance, coaching, and performance feedback to maximize employee productivity and job satisfaction., • Foster a positive work environment that encourages teamwork, professionalism, and exceptional customer service., • Set clear expectations and goals for the team and motivate them to achieve targets. Sales and Customer Service: • Develop and execute sales strategies to drive revenue growth and meet or exceed sales targets., • Monitor and analyse sales figures, identify trends, and implement necessary measures to optimize sales performance., • Ensure excellent customer service standards are maintained at all times, resolving customer issues and inquiries in a timely and satisfactory manner., • Build and maintain strong customer relationships, ensuring customer loyalty and repeat business. Store Operations and Merchandising: • Oversee the day-to-day operations of the store, including opening and closing procedures, cash management, and inventory control., • Ensure the store is clean, organized, and well-maintained to provide an inviting shopping environment., • Implement effective visual merchandising techniques to enhance product presentation and maximize sales opportunities., • Monitor and manage inventory levels, replenishment, and product ordering to avoid stockouts and minimize overstock situations. Financial Management: • Develop and manage the store's budget, including sales forecasts, expense control, and profitability analysis., • Monitor key performance indicators (KPIs) such as sales, gross margin, and labor costs to drive financial success., • Analyze financial reports, identify areas for improvement, and implement corrective actions as needed., • Control operational costs and minimize wastage to maximize profitability. Safety and Compliance: • Ensure compliance with all company policies, procedures, and legal regulations., • Maintain a safe working environment for employees and customers, following health and safety guidelines., • Stay updated with industry trends, market conditions, and competitors' activities to adapt strategies accordingly. Profile: • Proven experience as a Store Manager or in a similar role., • Strong leadership and people management skills., • Excellent communication and interpersonal abilities., • Sound knowledge of retail operations and merchandising techniques., • Proficient in analysing sales data and financial reports., • Ability to work under pressure and make effective decisions., • Familiarity with point-of-sale (POS) systems and inventory management software., • Flexibility to work evenings, weekends, and holidays as required., • Possibility of a permanent contract that will be evaluated with the candidate during the job interview. We are looking for a highly motivated individual who can represent our brand with enthusiasm and professionalism. The ideal candidate has experience driving CRM initiatives, strong attention to detail, and a results-oriented mindset. They possess a positive attitude and a genuine passion for the fashion industry. Send your cv:

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia, and the Americas. About the Role Due to our constant growth, we are looking for a Project Engineer - Pharmaceutical and Packaging Projects to support our projects in Parets del Vallès, Catalonia, Spain. Responsibilities • Managing the planning, execution, and successful completion of pharmaceutical and packaging projects., • Coordinating with cross-functional teams to ensure project timelines and objectives are achieved., • Supervising installation and commissioning of pharmaceutical and packaging equipment., • Conducting maintenance and troubleshooting activities to maintain optimal system performance., • Providing technical support and training to on-site personnel., • Ensuring strict compliance with industry standards and regulatory requirements., • Preparing detailed reports and documentation regarding project progress and equipment performance. Qualifications • Bachelor's degree in Engineering (Mechanical, Electrical, or Industrial)., • Minimum of 3 years' experience in the pharmaceutical and packaging industries., • Solid knowledge of pharmaceutical manufacturing and packaging processes and equipment., • Strong project management skills and high attention to detail., • Excellent communication and interpersonal skills., • Ability to work both independently and collaboratively., • Willingness to travel to various project sites as needed. Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome from the Hiring Manager interview, the recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills, and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia, and the Americas. About the Role Due to our constant growth, we are looking for a Project Engineer - Pharmaceutical and Packaging Projects to support our projects in Parets del Vallès, Catalonia, Spain. Responsibilities • Managing the planning, execution, and successful completion of pharmaceutical and packaging projects., • Coordinating with cross-functional teams to ensure project timelines and objectives are achieved., • Supervising installation and commissioning of pharmaceutical and packaging equipment., • Conducting maintenance and troubleshooting activities to maintain optimal system performance., • Providing technical support and training to on-site personnel., • Ensuring strict compliance with industry standards and regulatory requirements., • Bachelor's degree in Engineering (Mechanical, Electrical, or Industrial)., • Minimum of 3 years' experience in the pharmaceutical and packaging industries., • Solid knowledge of pharmaceutical manufacturing and packaging processes and equipment., • Strong project management skills and high attention to detail., • Excellent communication and interpersonal skills., • Ability to work both independently and collaboratively. Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome from the Hiring Manager interview, the recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills, and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

PHILIPP PLEIN is a highly successful luxury fashion brand. The driving force behind the company is human inspiration and creativity, with the goal of setting trends rather than following them. This strong belief has paved the way for the brand to become the international lifestyle label it is today. All our collections can be seen as works of art and are synonymous with nobility and perfection. Our daily challenge is always to live up to the expectations of our customers around the world. Duties and Responsibilities: • Leadership and Team Management:, • Recruit, train, and supervise store staff, including sales associates, cashiers, and stockroom personnel., • Provide guidance, coaching, and performance feedback to maximize employee productivity and job satisfaction., • Foster a positive work environment that encourages teamwork, professionalism, and exceptional customer service., • Develop and execute sales strategies to drive revenue growth and meet or exceed sales targets., • Monitor and analyse sales figures, identify trends, and implement necessary measures to optimize sales performance., • Ensure excellent customer service standards are maintained at all times, resolving customer issues and inquiries in a timely and satisfactory manner., • Oversee the day-to-day operations of the store, including opening and closing procedures, cash management, and inventory control., • Ensure the store is clean, organized, and well-maintained to provide an inviting shopping environment., • Implement effective visual merchandising techniques to enhance product presentation and maximize sales opportunities., • Develop and manage the store's budget, including sales forecasts, expense control, and profitability analysis., • Monitor key performance indicators (KPIs) such as sales, gross margin, and labor costs to drive financial success., • Analyze financial reports, identify areas for improvement, and implement corrective actions as needed., • Ensure compliance with all company policies, procedures, and legal regulations., • Maintain a safe working environment for employees and customers, following health and safety guidelines., • Proven experience as a Store Manager or in a similar role., • Strong leadership and people management skills., • Excellent communication and interpersonal abilities., • Sound knowledge of retail operations and merchandising techniques., • Proficient in analysing sales data and financial reports., • Ability to work under pressure and make effective decisions., • Familiarity with point-of-sale (POS) systems and inventory management software., • Flexibility to work evenings, weekends, and holidays as required. Send your cv:

We're Hiring: Full-Time Dentist at CeraRoot CLINIC (Barcelona) CeraRoot CLINIC is expanding! We’re looking for a motivated and skilled full-time dentist to join our multidisciplinary team in Barcelona, where innovation meets clinical excellence. About the Role As part of our clinical team, you’ll be responsible for: • Treating patients with a biological and holistic approach, • Designing and planning treatments using CAD/CAM digital workflows, • Collaborating with our Quality Department to ensure compliance What We Offer • Full-time contract, • Structured training and career development, • A dynamic work environment at the forefront of digital technology and ceramic implantology, • Opportunity to grow within an internationally recognized company Requirements • Degree in Dentistry, • Ideally a smart young dentist with Interest to grow in multiple areas of dentistry, including digital dentistry, cad/cam design and production, ceramic implantology and metal-free dentistry, • Comfortable with technology and digital dentistry, • Team player with a patient-centered mindset, • English and Spanish (working proficiency) Location: CeraRoot CLINIC – Les Franqueses del Valles , Barcelona, Spain Start date: As soon as possible Interested or know someone who might be a great fit? Apply now or message us directly for more details! #Dentist #HiringDentist #DentalJobs #BarcelonaJobs #CeraRoot #BiologicalDentistry #CADCAM #CeramicImplants #FullTimeJob

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia, and the Americas. About the Role Due to our constant growth, we are looking for a Project Engineer - Pharmaceutical and Packaging Projects to support our projects in Parets del Vallès, Catalonia, Spain. Responsibilities • Managing the planning, execution, and successful completion of pharmaceutical and packaging projects., • Coordinating with cross-functional teams to ensure project timelines and objectives are achieved., • Supervising installation and commissioning of pharmaceutical and packaging equipment., • Conducting maintenance and troubleshooting activities to maintain optimal system performance., • Providing technical support and training to on-site personnel., • Ensuring strict compliance with industry standards and regulatory requirements., • Preparing detailed reports and documentation regarding project progress and equipment performance. Qualifications • Bachelor's degree in Engineering (Mechanical, Electrical, or Industrial)., • Minimum of 3 years' experience in the pharmaceutical and packaging industries., • Solid knowledge of pharmaceutical manufacturing and packaging processes and equipment., • Strong project management skills and high attention to detail., • Excellent communication and interpersonal skills., • Ability to work both independently and collaboratively., • Willingness to travel to various project sites as needed. Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome from the Hiring Manager interview, the recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills, and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

🔹 We're Hiring: Full-Time Dentist at CeraRoot CLINIC (Barcelona) 🔹 CeraRoot CLINIC is expanding! We’re looking for a motivated and skilled full-time dentist to join our multidisciplinary team in Barcelona, where innovation meets clinical excellence. 🦷 About the Role As part of our clinical team, you’ll be responsible for: • Treating patients with a biological and holistic approach, • Designing and planning treatments using CAD/CAM digital workflows, • Collaborating with our Quality Department to ensure compliance 🌱 What We Offer • Full-time contract, • Structured training and career development, • A dynamic work environment at the forefront of digital technology and ceramic implantology, • Opportunity to grow within an internationally recognized company ✅ Requirements • Degree in Dentistry, • Ideally a smart young dentist with Interest to grow in multiple areas of dentistry, including digital dentistry, cad/cam design and production, ceramic implantology and metal-free dentistry, • Comfortable with technology and digital dentistry, • Team player with a patient-centered mindset, • English and Spanish (working proficiency) 📍Location: CeraRoot CLINIC – Les Franqueses del Valles , Barcelona, Spain 🕒 Start date: As soon as possible Interested or know someone who might be a great fit? 👉 Apply now or message us directly for more details! #Dentist #HiringDentist #DentalJobs #BarcelonaJobs #CeraRoot #BiologicalDentistry #CADCAM #CeramicImplants #FullTimeJob

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia, and the Americas. About the Role Due to our constant growth, we are looking for a Project Engineer - Pharmaceutical and Packaging Projects to support our projects in Parets del Vallès, Catalonia, Spain. Responsibilities • Managing the planning, execution, and successful completion of pharmaceutical and packaging projects., • Coordinating with cross-functional teams to ensure project timelines and objectives are achieved., • Supervising installation and commissioning of pharmaceutical and packaging equipment., • Conducting maintenance and troubleshooting activities to maintain optimal system performance., • Providing technical support and training to on-site personnel., • Ensuring strict compliance with industry standards and regulatory requirements., • Preparing detailed reports and documentation regarding project progress and equipment performance. Qualifications • Bachelor's degree in Engineering (Mechanical, Electrical, or Industrial)., • Minimum of 3 years' experience in the pharmaceutical and packaging industries., • Solid knowledge of pharmaceutical manufacturing and packaging processes and equipment., • Strong project management skills and high attention to detail., • Excellent communication and interpersonal skills., • Ability to work both independently and collaboratively., • Willingness to travel to various project sites as needed. Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome from the Hiring Manager interview, the recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills, and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

PHILIPP PLEIN is a highly successful luxury fashion brand. The driving force behind the company is human inspiration and creativity, with the goal of setting trends rather than following them. This strong belief has paved the way for the brand to become the international lifestyle label it is today. All our collections can be seen as works of art and are synonymous with nobility and perfection. Our daily challenge is always to live up to the expectations of our customers around the world. Duties and Responsibilities: • Leadership and Team Management:, • Recruit, train, and supervise store staff, including sales associates, cashiers, and stockroom personnel., • Provide guidance, coaching, and performance feedback to maximize employee productivity and job satisfaction., • Foster a positive work environment that encourages teamwork, professionalism, and exceptional customer service., • Set clear expectations and goals for the team and motivate them to achieve targets. Sales and Customer Service: • Develop and execute sales strategies to drive revenue growth and meet or exceed sales targets., • Monitor and analyse sales figures, identify trends, and implement necessary measures to optimize sales performance., • Ensure excellent customer service standards are maintained at all times, resolving customer issues and inquiries in a timely and satisfactory manner., • Build and maintain strong customer relationships, ensuring customer loyalty and repeat business. Store Operations and Merchandising: • Oversee the day-to-day operations of the store, including opening and closing procedures, cash management, and inventory control., • Ensure the store is clean, organized, and well-maintained to provide an inviting shopping environment., • Implement effective visual merchandising techniques to enhance product presentation and maximize sales opportunities., • Monitor and manage inventory levels, replenishment, and product ordering to avoid stockouts and minimize overstock situations. Financial Management: • Develop and manage the store's budget, including sales forecasts, expense control, and profitability analysis., • Monitor key performance indicators (KPIs) such as sales, gross margin, and labor costs to drive financial success., • Analyze financial reports, identify areas for improvement, and implement corrective actions as needed., • Control operational costs and minimize wastage to maximize profitability. Safety and Compliance: • Ensure compliance with all company policies, procedures, and legal regulations., • Maintain a safe working environment for employees and customers, following health and safety guidelines., • Stay updated with industry trends, market conditions, and competitors' activities to adapt strategies accordingly. Profile: • Proven experience as a Store Manager or in a similar role., • Strong leadership and people management skills., • Excellent communication and interpersonal abilities., • Sound knowledge of retail operations and merchandising techniques., • Proficient in analysing sales data and financial reports., • Ability to work under pressure and make effective decisions., • Familiarity with point-of-sale (POS) systems and inventory management software., • Flexibility to work evenings, weekends, and holidays as required., • Possibility of a permanent contract that will be evaluated with the candidate during the job interview. We are looking for a highly motivated individual who can represent our brand with enthusiasm and professionalism. The ideal candidate has experience driving CRM initiatives, strong attention to detail, and a results-oriented mindset. They possess a positive attitude and a genuine passion for the fashion industry. Send your cv:

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia, and the Americas. About the Role Due to our constant growth, we are looking for a Project Engineer - Pharmaceutical and Packaging Projects to support our projects in Parets del Vallès, Catalonia, Spain. Responsibilities • Managing the planning, execution, and successful completion of pharmaceutical and packaging projects., • Coordinating with cross-functional teams to ensure project timelines and objectives are achieved., • Supervising installation and commissioning of pharmaceutical and packaging equipment., • Conducting maintenance and troubleshooting activities to maintain optimal system performance., • Providing technical support and training to on-site personnel., • Ensuring strict compliance with industry standards and regulatory requirements., • Preparing detailed reports and documentation regarding project progress and equipment performance. Qualifications • Bachelor's degree in Engineering (Mechanical, Electrical, or Industrial)., • Minimum of 3 years' experience in the pharmaceutical and packaging industries., • Solid knowledge of pharmaceutical manufacturing and packaging processes and equipment., • Strong project management skills and high attention to detail., • Excellent communication and interpersonal skills., • Ability to work both independently and collaboratively., • Willingness to travel to various project sites as needed. Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome from the Hiring Manager interview, the recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills, and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Immunoassay business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Within a medical device environment, work with the QARA Manager to ensure regulatory compliance and certification of software products. Key Accountabilities Be a key part of a team where you will: • Collaborate in maintaining the quality system documentation processes and procedures adopted by the company., • Investigate and resolve quality issues, implementing corrective and preventive actions to mitigate recurrence., • Coordinate and support the preparation of software technical documents appropriate for regulatory submissions., • Support the regulatory submissions for market authorization for medical device products., • Conduct internal assessments and audits to identify areas for improvement and ensure adherence to established procedures., • Facilitate the approval process for software releases., • Disseminating knowledge about the Quality System and regulatory requirements., • Review Promotional and advertising materials., • Oversee post-market surveillance activities related to medical device products. The main relationships within to the Werfen Group are: • QARA Manger, QA Leads, Validation Led, • Factory Lead and Solution Leaders, • Customer, • Application Lifecycle manager (ALM), • Notified Bodies and Competent Authorities for product regulatory compliance., • Engineer, computer Science or other Technical carrier, or equivalent work experience., • A minimum of 5 years experience in Quality Assurance or Regulatory related, preferably within the Healthcare sector, • Additional Skills/Knowledge:, • Knowledge and experience working with medical device international regulations and related standards (ISO 13485, ISO 14971,..)., • Knowledge and experience working in Medical device software life cycle process (IEC 62304), • Desirable:, • Knowledge and experience working in medical device regulatory submissions (MDR/IVDR,FDA..) The ideal candidate for this position will exhibit the following skills and competencies: • Good level of Technical and Conversional English., • Team player with ability to work independently., • Excellent and effective written and verbal communication skills., • Excellent interpersonal skills, good judgment and analytical skills., • A meaningful project that will impact the quality of laboratory software medicine worldwide, • 3 days a week working from home, • Multicultural and friendly team, • Exciting opportunities for professional development., • Ongoing training, • Social benefits: Canteen, nursery check, English training... JOIN US!

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Immunoassay business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Within a medical device environment, work with the QARA Manager to ensure regulatory compliance and certification of software products. Key Accountabilities Be a key part of a team where you will: • Collaborate in maintaining the quality system documentation processes and procedures adopted by the company., • Investigate and resolve quality issues, implementing corrective and preventive actions to mitigate recurrence., • Coordinate and support the preparation of software technical documents appropriate for regulatory submissions., • Support the regulatory submissions for market authorization for medical device products., • Conduct internal assessments and audits to identify areas for improvement and ensure adherence to established procedures., • Facilitate the approval process for software releases., • Disseminating knowledge about the Quality System and regulatory requirements., • Review Promotional and advertising materials., • Oversee post-market surveillance activities related to medical device products., • Offer guidance and mentorship to QARA team members at lower levels Networking/Key relationships The main relationships within to the Werfen Group are: • QARA Manger, QA Leads, Validation Led, • Factory Lead and Solution Leaders, • Customer, • Application Lifecycle manager (ALM), • Notified Bodies and Competent Authorities for product regulatory compliance., • This position may also require also cooperating with other companies inside Werfen. Minimum Knowledge & Experience required for the position: • Engineer, computer Science or other Technical carrier, or equivalent work experience., • A minimum of 5 years experience in Quality Assurance or Regulatory related, preferably within the Healthcare sector, • Additional Skills/Knowledge:, • Knowledge and experience working with medical device international regulations and related standards (ISO 13485, ISO 14971,..)., • Knowledge and experience working in Medical device software life cycle process (IEC 62304), • Desirable:, • Knowledge and experience working in medical device regulatory submissions (MDR/IVDR,FDA..), • Internal auditor qualification for management systems or knowledge of auditing techniques Skills & Capabilities: The ideal candidate for this position will exhibit the following skills and competencies: • Good level of Technical and Conversional English., • Team player with ability to work independently., • Excellent and effective written and verbal communication skills., • Excellent interpersonal skills, good judgment and analytical skills., • Effective time management and organizational skills What we offer: • A meaningful project that will impact the quality of laboratory software medicine worldwide, • 3 days a week working from home, • Multicultural and friendly team, • Exciting opportunities for professional development., • Ongoing training, • Social benefits: Canteen, nursery check, English training..., • All the benefits according to the chemical agreement Our Purpose: We contribute to the advancement of patient care around the world through innovative specialized diagnostics JOIN US!

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia, and the Americas. About the Role Due to our constant growth, we are looking for a Project Engineer - Pharmaceutical and Packaging Projects to support our projects in Parets del Vallès, Catalonia, Spain. Responsibilities Managing the planning, execution, and successful completion of pharmaceutical and packaging projects. Coordinating with cross-functional teams to ensure project timelines and objectives are achieved. Supervising installation and commissioning of pharmaceutical and packaging equipment. Conducting maintenance and troubleshooting activities to maintain optimal system performance. Providing technical support and training to on-site personnel. Ensuring strict compliance with industry standards and regulatory requirements. Preparing detailed reports and documentation regarding project progress and equipment performance. Qualifications Bachelor's degree in Engineering (Mechanical, Electrical, or Industrial). Minimum of 3 years' experience in the pharmaceutical and packaging industries. Solid knowledge of pharmaceutical manufacturing and packaging processes and equipment. Strong project management skills and high attention to detail. Excellent communication and interpersonal skills. Ability to work both independently and collaboratively. Willingness to travel to various project sites as needed. Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome from the Hiring Manager interview, the recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills, and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Fedefarma, located in Palau-solità i Plegamans, Catalonia, Spain, is seeking a Director/a Tècnic/a Suplent to join our team. We value the success of our projects as a result of our dedicated personnel. With nearly 100 years of experience, we understand that change is constant and embrace adaptation, excellence, and determination. If you wish to grow as a Director/a Tècnic/a and in the Quality field, and want to advance your professional career with opportunities and growth, continue reading, as this role is for you. We are a cooperative with over 95 years of history serving the health sector and supporting pharmacies. We are leaders in pharmaceutical distribution in Catalonia, present in the Valencian Community, Murcia, and Andorra, and expanding to new regions in Spain by 2025. Our core values include proximity, transparency, honesty, passion, and innovation. The role involves ensuring compliance with BPDs to keep warehouses operational, implementing improvement actions, and supporting all centers in TDA tasks. Responsibilities include: • Monitoring and implementing BPDs at the warehouse., • Technical Department tasks., • Managing health alerts, controlled substances, inspections, and documentation., • Managing quality indicators, partner and client relations, and technical support., • Handling documentation, alerts, temperature-controlled materials, and transport in Andorra., • Are graduates in Pharmacy with BPD training., • Have at least 1 year of experience as a Technical Director in Quality Assurance and Technical Management., • Have experience in pharmacy offices., • Possess knowledge of ERP environments, BPDs, and ISO standards., • Experience in pharmaceutical distribution is highly valued., • Have excellent teamwork, communication, organizational, time management, and problem-solving skills., • Are adaptable to changing environments and situations., • Being part of a competitive, leading, and continuously growing company., • Opportunities for professional development and growth., • Permanent position with a competitive salary policy., • Flexible benefits (Mútua, Meal and Childcare tickets). Palau-solità i Plegamans, Catalonia, Spain #J-18808-Ljbffr

Esta persona reportará a la Chief Compliance Officer del Grupo y contribuirá activamente al desarrollo y ejecución del programa de Compliance Assurance, enfocado en verificar la implementación efectiva del modelo de Compliance de Applus+ en todas las entidades del Grupo. Mínimo 10 años de expe

Esta persona reportará a la Chief Compliance Officer del Grupo y contribuirá activamente al desarrollo y ejecución del programa de Compliance Assurance, enfocado en verificar la implementación efectiva del modelo de Compliance de Applus+ en todas las entidades del Grupo. Colaborar en el diseño

Coordinate and maintain documentation to support audits and ensure compliance with established standards.

The officer will work cross-functionally with global legal, compliance, supply chain, commercial, and IT teams to ensure the effective alignment of trade compliance across the business. Employee Training: Design and deliver global training programs on trade compliance topics tailored to roles, regio

We work with multinational corporations to help structure their departments with the best people, from the Global Chief Compliance Officer and General Counsel to the Compliance Analyst and Trade Compliance Specialist. Leonid Group Corporate Governance is a talent acquisition consultancy that special

Maintaining an up to date schedule of reporting requirements across jurisdictions and ensuring timely submission in coordination with the Head of Compliance and local Compliance Officers / Directors;. Regular maintenance of all Group & Regulated Entities’ compliance policies, such as AML manual, R

Tendrás un papel esencial en la gestión operativa del área fiscal, con responsabilidad en la revisión y presentación de modelos, control de notificaciones, coordinación con proveedores y apoyo a procesos contables y de auditoría.Es una posición ideal para perfiles con experiencia en gestorí

Tendrás un papel esencial en la gestión operativa del área fiscal, con responsabilidad en la revisión y presentación de modelos, control de notificaciones, coordinación con proveedores y apoyo a procesos contables y de auditoría.Es una posición ideal para perfiles con experiencia en gestorí

Global Compliance and Reporting (GCR) team. Lead and support the transition process for accounting and compliance services—from client handover to hypercare phase. Good understanding of accounting/reporting processes, financial controls, and compliance obligations.

Colaborar con la Senior Compliance garantizando el cumplimiento de las obligaciones legales y de cumplimiento, contribuyendo a crear un entorno de control. Colaborar con los asesores externos en materia de Protección de Datos, Compliance Penal y entidades regulatorias.

Colaborar con la Senior Compliance garantizando el cumplimiento de las obligaciones legales y de cumplimiento, contribuyendo a crear un entorno de control. Colaborar con los asesores externos en materia de Protección de Datos, Compliance Penal y entidades regulatorias.

Coordinate and maintain documentation to support audits and ensure compliance with established standards.

Maintaining an up to date schedule of reporting requirements across jurisdictions and ensuring timely submission in coordination with the Head of Compliance and local Compliance Officers / Directors;. Coordinating preparation for the annual AML audit along with Head of Compliance;. Experience liaisi

Forvis Mazars es la nueva red formada por Forvis, una de las principales compañías en el sector de los servicios profesionales en Estados Unidos, y Mazars firma internacional que operaba ya en más de 100 países.Forvis Mazars opera actualmente como una red global en más de 100 países, 400 ofici

Coordinate and maintain documentation to support audits and ensure compliance with established standards.

Compliance Certification: Lead the global annual compliance certification process, ensuring clarity, accountability, and tracking of attestation across all functions and geographies. Familiarity with digital compliance tools and data-based decision making. The Global Governance & Engagement Officer

We work with multinational corporations to help structure their departments with the best people, from the Global Chief Compliance Officer and General Counsel to the Compliance Analyst and Trade Compliance Specialist. Leonid Group Corporate Governance is a talent acquisition consultancy that special

We work with multinational corporations to help structure their departments with the best people, from the Global Chief Compliance Officer and General Counsel to the Compliance Analyst and Trade Compliance Specialist. Leonid Group Corporate Governance is a talent acquisition consultancy that special

Tendrás un papel esencial en la gestión operativa del área fiscal, con responsabilidad en la revisión y presentación de modelos, control de notificaciones, coordinación con proveedores y apoyo a procesos contables y de auditoría.Es una posición ideal para perfiles con experiencia en gestorí

Lead and support the transition process for accounting and compliance services—from client handover to hypercare phase. Good understanding of accounting/reporting processes, financial controls, and compliance obligations. Global Compliance and Reporting (GCR) team.

Maintaining an up to date schedule of reporting requirements across jurisdictions and ensuring timely submission in coordination with the Head of Compliance and local Compliance Officers / Directors;. Experience liaising with Compliance officers / MLROs, Product & Sales, banks, auditors and regulato

You’ll be responsible for managing the compliance roadmap, working closely with Legal, Compliance, and Engineering teams to ensure the platform evolves in line with new legislation and market demands. I’m working with a leading iGaming platform provider who are looking to hire an experienced Pro

The Global Trade Compliance Officer is responsible for developing, implementing, and continuously enhancing Werfen’s worldwide trade compliance strategy. Employee Training: Design and deliver global training programs on trade compliance topics tailored to roles, regions, and risk levels; promote a

Reporting to the Head of Information Security, he/she will play a critical role in enabling company growth by ensuring regulatory readiness, managing risk, and embedding security and compliance into business and product operations. Lead the implementation of GDPR, ISO 27001, SOC 2, and NIS 2 complia

You’ll be responsible for managing the compliance roadmap, working closely with Legal, Compliance, and Engineering teams to ensure the platform evolves in line with new legislation and market demands. Strong experience working on compliance-related product features or core platform functionality.

He/She will be responsible for designing and operationalizing the company’s governance, risk, and compliance framework. Act as the primary liaison for compliance-related queries from clients, partners, and regulators. Familiarity with compliance automation platforms (e.

At least 5 years of experience in the aeronautical sector, including audit and compliance roles. Maintain and continuously improve the quality and compliance management system. Act as the main point of contact for regulatory compliance within Operations.

You’ll be responsible for managing the compliance roadmap, working closely with Legal, Compliance, and Engineering teams to ensure the platform evolves in line with new legislation and market demands. I’m working with a leading iGaming platform provider who are looking to hire an experienced Pro

Do you enjoy helping customers succeed while navigating cybersecurity and compliance challenges in a fast-moving startup? Look no further. We’re looking for a Cybersecurity & Compliance Specialist who’s comfortable working with technical tools and concepts to join our team. In this role, you’l

You’ll be responsible for managing the compliance roadmap, working closely with Legal, Compliance, and Engineering teams to ensure the platform evolves in line with new legislation and market demands. This is a key role for someone who understands the challenges of regulatory compliance in iGaming

Familiarity with compliance automation platforms (e. Governance Risk & Compliance Lead. Reporting to the Head of Information Security, he/she will play a critical role in enabling company growth by ensuring regulatory readiness, managing risk, and embedding security and compliance into business and