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At iVascular, we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of cardio, neuro, and endovascular diseases and to become a reference in the vascular field by enhancing the value of technology and innovation. We are a national company founded in 2010 in Barcelona (Spain) in a phase of growth and international expansion, with subsidiaries already established in Europe, Latin America, Canada, and China, and a team of more than 550 employees covering the entire manufacturing process through vertical integration. We are currently looking for an R&D PROJECT LEADER for our plant located in Sant Vicenç dels Horts (Barcelona). Your main objective will be to lead the development of a delivery system for a medical device, from 2D/3D prototype design to the management of prototype manufacturing, coordination of bench testing, analysis of results and report writing, leading the device verification phase, and preparing the necessary documentation for submission to regulatory authorities. KEY RESPONSIBILITIES: • Prepare the technical planning for assigned projects, applying the methodology implemented in the company., • In collaboration with the department head, prepare project budgets and define the technical and human resources to achieve the technical and economic objectives., • Ensure the feasibility and technical quality of the solutions proposed., • Coordinate and implement the production process for the products developed., • Research and develop improvements in the technical characteristics, quality, and costs of products., • Define purchasing specifications and approve suppliers from the initial stage until the product is transferred to the factory, sending guidelines for subsequent procurement. DESIRED PROFILE: • Industrial Engineering, especially in the mechanical, electromechanical, materials, biomedical fields or a similar one., • High level of English and Spanish., • Minimum 5 years of experience in a similar position., • Previous experience working in an R&D department. Previous experience working with CAD systems (especially Solidworks and Rhinoceros) and Ansys., • High capacity for multidisciplinary work, analytical capacity, integrity, cooperative spirit, communication skills. Innovative sense, high self-esteem, and high expectations for professional development. WHAT WE OFFER: • Permanent and stable contract in a project with high global impact and expanding internationally., • Professional and personal development in a vibrant, dynamic, and youthful environment., • Competitive salary tailored to your experience, along with an attractive benefits package., • Flexible working hours to support a healthy work-life balance., • Flexible compensation (meal vouchers, transportation, and childcare assistance)., • Access to our iWellness program: gym and physiotherapist on site., • Corporate events and gifts., • Subsidized on-site company cafeteria.

At iVascular, we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of cardio, neuro, and endovascular diseases and to become a reference in the vascular field by enhancing the value of technology and innovation. We are a national company founded in 2010 in Barcelona (Spain) in a phase of growth and international expansion, with subsidiaries already established in Europe, Latin America, Canada, and China, and a team of more than 550 employees covering the entire manufacturing process through vertical integration. We are currently seeking a passionate and experienced Clinical Evaluation Specialist to join our Clinical team at our site in Sant Vicenç dels Horts (Barcelona). You will be responsible for the development a creation of Clinical Documents in accordance the European Medical Device Regulation conducting literature reviews and writing Clinical Evaluation Reports. KEY RESPONSIBILITIES: • Development, writing and validation of Clinical Evaluation Reports (CERs) and Clinical Evaluation Plans (CEPs)., • Execute comprehensive systematic literature reviews, ensuring robust methodology, full traceability and appropriate use of specialized scientific databases., • Prepare Literature Seach Reports., • Critically appraise clinical evidence (manufacturer-held data and published literature) to support conclusions on device safety and performance in accordance with EU MDR. Review and prepare key clinical MDR documentation, including: • CDP (clinical development plan)., • PMCF-plan (post market clinical follow-plan), • PMCF Reports., • SSCPs (Sammery of safety and clinical performance). Develop, write and update key clinical documentation, including: • Literature Search Reports., • Clinical Evaluation Reports., • Clinical Evaluation Plans (CEP)., • PMCF Plans and PMCF Reports., • SSCPs., • Support the clinical evaluation strategy across the medical device portfolio, in close collaboration with Regulatory Affairs and Quality teams., • Contribute to Post-Market Surveillance (PMS) activities, including PSURs and PMCF-related documentation., • Interact with Notified Bodies and Competent Authorities in relation to clinical documentation and regulatory queries., • Ensure all clinical documentation complies with EU MDR 2017/745, MEDDEV guidance and applicable MDCG documents. DESIRED PROFILE: • Scientific or medical background (Biomedical Sciences, Life Sciences, Biotechnology, Pharmacy or similar)., • Minimum of 3 years of hands-on experience in Clinical Evaluation of medical devices under EU MDR 2017/745., • Proven hands-on experience authoring and updating:, • CERs, • CEPs, • PMCF Plans & Reports, • SSCPs, • Solid understanding of:, • MEDDEV 2.7/1 Rev.4, • MDCG guidance, • Post-market clinical requirements., • Experience interacting with Notified Bodies regarding clinical documentation is highly valued., • Strong expertise in scientific writing, literature appraisal and systematic literature searches., • Familiarity with reference management tools (Zotero, Mendeley or similar)., • Fluent English and Spanish (written and spoken). WHAT WE OFFER: • Permanent and stable contract in a project with high global impact and expanding internationally., • Professional and personal development in a vibrant, dynamic, and youthful environment., • Competitive salary tailored to your experience, along with an attractive benefits package., • Hybrid working model with telework days, and flexible hours. From Monday to Thursday, start between 7:00 and 9:00 a.m. and finish from 4:30 p.m. onwards. On Fridays, enjoy an intensive schedule from 8:00 a.m. to 2:00 p.m., • Flexible compensation (meal vouchers, transportation, and childcare assistance)., • Access to our iWellness program: gym and physiotherapist on site., • Corporate events and gifts., • Subsidized on-site company cafeteria.

At iVascular, we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of cardio, neuro, and endovascular diseases and to become a reference in the vascular field by enhancing the value of technology and innovation. We are a national company founded in 2010 in Barcelona (Spain) in a phase of growth and international expansion, with subsidiaries already established in Europe, Latin America, Canada, and China, and a team of more than 550 employees covering the entire manufacturing process through vertical integration. We are currently seeking a passionate and experienced Head of Clinical Evaluation to join our Clinical team at our site in Sant Vicenç dels Horts (Barcelona). You will be responsible for leading the Clinical Evaluation unit, driving the company’s clinical strategy. You will oversee the development, writing and supervision of all key clinical documentation, ensuring high-quality Clinical Evaluation Reports (CER), systematic literature reviews always in full compliance with the European Medical Device Regulation (MDR). KEY RESPONSIBILITIES: • Lead the Clinical Evaluation unit, managing the team and ensuring alignment with the company’s overall clinical strategy., • Coordinate and contribute to the development, writing, validation and approval of Clinical Evaluation Reports (CERs) and Literature Search Reports., • Oversee comprehensive systematic literature reviews, ensuring robust methodology, full traceability and the appropriate use of specialized databases., • Critically appraise all available clinical evidence—both internal data and published literature—to support well-founded conclusions on device safety and performance., • Review and prepare key clinical MDR documentation, including CEP (clinical evaluation plan), CDP (clinical development plan), PMCF-plan (post market clinical follow-plan), PMCF Reports, SSCPs (Sammery of safety and clinical performance). DESIRED PROFILE: • Bachelor’s degree in Health Sciences, Biotechnology, Biomedicine, or a related scientific field, • PhD or equivalent advanced scientific background, is a strong asset., • High level of English and Spanish., • 5 years of experience with EU MDR 2017/745, including extensive authorship, review and approval of CERs and clinical documentation., • Strong experience authoring PMCF Reports, SSCPs, Clinical Evaluation Plans (CEP) and Clinical Evaluation Reports (CER)., • Experience with clinical investigation standard WHAT WE OFFER: • Permanent and stable contract in a project with high global impact and expanding internationally., • Professional and personal development in a vibrant, dynamic, and youthful environment., • Competitive salary tailored to your experience, along with an attractive benefits package., • Flexible working hours to support a healthy work-life balance., • Flexible compensation (meal vouchers, transportation, and childcare assistance)., • Access to our iWellness program: gym and physiotherapist on site., • Corporate events and gifts., • Subsidized on-site company cafeteria.

¿Te gustaría unirte a un entorno internacional, dinámico y con un fuerte portfolio de marcas premium? Si tienes experiencia administrativa vinculada a tareas contables y dominas español y portugués, ¡esta oportunidad puede ser para ti! 🕶️ Sobre Marchon Eyewear Marchon Eyewear es uno de los principales actores mundiales en el sector de la óptica y gafas de sol. La compañía comercializa sus productos bajo marcas de prestigio como Calvin Klein, Calvin Klein Jeans, Canada Goose, Converse, DKNY, Dragon, Karl Lagerfeld, Lacoste, Liu Jo, Longchamp, Nike, Paul Smith, Salvatore Ferragamo y Skaga. Nuestro portafolio cubre los segmentos clave del mercado premium. Distribuimos a más de 80.000 clientes en más de 100 países a través de una red global de filiales y distribuidores. Marchon forma parte del grupo VSP Vision, líder mundial en salud visual (). 🔍 Tu día a día Formarás parte del departamento contable, apoyando en tareas administrativas y en gestiones relacionadas con clientes, proveedores y bancos. Entre tus responsabilidades estarán: • Gestión administrativa y contable en clientes y proveedores (AR & AP)., • Atención telefónica y resolución de consultas por email., • Registro y archivo de documentos de facturación., • Conciliación diaria de movimientos bancarios., • Soporte en la contabilización y conciliación de cuentas., • Colaboración en cierres mensuales/trimestrales/anuales., • Preparación de documentación para auditoría., • Elaboración de liquidaciones de comisiones y bonus., • Presentación de documentación tributaria y reglamentaria., • Mejora de procedimientos administrativos y contables., • Colaboración con otros equipos en actividades administrativas y financieras. 🎯 Requisitos • Experiencia previa en tareas administrativas dentro de un entorno contable (no es imprescindible experiencia íntegra como contable)., • Alto nivel de portugués y español (oral y escrito)., • Valorable experiencia con herramientas ERP y hojas de cálculo (Excel)., • Se valorará conocimiento de inglés y/o SAP., • Persona organizada, metódica, con atención al detalle y capacidad para gestionar varias tareas., • Comunicación efectiva y buena capacidad para resolver incidencias., • Capacidad para mantener registros actualizados y bien documentados. 💼 Condiciones de trabajo • Contrato temporal (6 meses), • Media jornada: 20 horas semanales (lunes a viernes)., • Modelo híbrido de trabajo (etapa inicial presencial por formación)., • Salario acorde al mercado. Si te motiva formar parte de un equipo internacional, profesional y con marcas líderes a nivel mundial, ¡queremos conocerte!

At iVascular , we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of cardio , neuro , and endovascular diseases and to become a reference in the vascular field by enhancing the value of technology and innovation. We are a national company founded in 2010 in Barcelona (Spain) in a phase of growth and international expansion, with subsidiaries already established in Europe, Latin America, Canada, and China, and a team of more than 550 employees covering the entire manufacturing process through vertical integration. We are currently seeking a passionate and experienced Clinical Evaluation Specialist to join our Clinical team at our site in Sant Vicenç dels Horts (Barcelona). You will be responsible for the development a creation of Clinical Documents in accordance the European Medical Device Regulation conducting literature reviews and writing Clinical Evaluation Reports. KEY RESPONSIBILITIES: Development, writing and validation of Clinical Evaluation Reports (CERs) and Clinical Evaluation Plans (CEPs). Execute comprehensive systematic literature reviews , ensuring robust methodology, full traceability and appropriate use of specialized scientific databases. Prepare Literature Seach Reports. Critically appraise clinical evidence (manufacturer-held data and published literature) to support conclusions on device safety and performance in accordance with EU MDR. Review and prepare key clinical MDR documentation, including: CDP (clinical development plan). PMCF-plan (post market clinical follow-plan) PMCF Reports. SSCPs (Sammery of safety and clinical performance). Develop, write and update key clinical documentation, including: Literature Search Reports. Clinical Evaluation Reports. Clinical Evaluation Plans (CEP). PMCF Plans and PMCF Reports. SSCPs. Support the clinical evaluation strategy across the medical device portfolio, in close collaboration with Regulatory Affairs and Quality teams. Contribute to Post-Market Surveillance (PMS) activities, including PSURs and PMCF-related documentation. Interact with Notified Bodies and Competent Authorities in relation to clinical documentation and regulatory queries. Ensure all clinical documentation complies with EU MDR 2017/745 , MEDDEV guidance and applicable MDCG documents. DESIRED PROFILE: Scientific or medical background (Biomedical Sciences, Life Sciences, Biotechnology, Pharmacy or similar). Minimum of 3 years of hands-on experience in Clinical Evaluation of medical devices under EU MDR 2017/745 . Proven hands-on experience authoring and updating: CERs CEPs PMCF Plans & Reports SSCPs Solid understanding of: MEDDEV 2.7/1 Rev.4 MDCG guidance Post-market clinical requirements. Experience interacting with Notified Bodies regarding clinical documentation is highly valued. Strong expertise in scientific writing, literature appraisal and systematic literature searches . Familiarity with reference management tools (Zotero, Mendeley or similar). Fluent English and Spanish (written and spoken). WHAT WE OFFER: Permanent and stable contract in a project with high global impact and expanding internationally. Professional and personal development in a vibrant, dynamic, and youthful environment. Competitive salary tailored to your experience, along with an attractive benefits package. Hybrid working model with telework days, and flexible hours. From Monday to Thursday, start between 7:00 and 9:00 a.m. and finish from 4:30 p.m. onwards. On Fridays, enjoy an intensive schedule from 8:00 a.m. to 2:00 p.m. Flexible compensation (meal vouchers, transportation, and childcare assistance). Access to our iWellness program: gym and physiotherapist on site. Corporate events and gifts. Subsidized on-site company cafeteria.

At iVascular , we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of cardio , neuro , and endovascular diseases and to become a reference in the vascular field by enhancing the value of technology and innovation. We are a national company founded in 2010 in Barcelona (Spain) in a phase of growth and international expansion, with subsidiaries already established in Europe, Latin America, Canada, and China, and a team of more than 550 employees covering the entire manufacturing process through vertical integration. We are currently seeking a passionate and experienced Clinical Evaluation Specialist to join our Clinical team at our site in Sant Vicenç dels Horts (Barcelona). You will be responsible for the development a creation of Clinical Documents in accordance the European Medical Device Regulation conducting literature reviews and writing Clinical Evaluation Reports. KEY RESPONSIBILITIES: Development, writing and validation of Clinical Evaluation Reports (CERs) and Clinical Evaluation Plans (CEPs). Execute comprehensive systematic literature reviews , ensuring robust methodology, full traceability and appropriate use of specialized scientific databases. Prepare Literature Seach Reports. Critically appraise clinical evidence (manufacturer-held data and published literature) to support conclusions on device safety and performance in accordance with EU MDR. Review and prepare key clinical MDR documentation, including: CDP (clinical development plan). PMCF-plan (post market clinical follow-plan) PMCF Reports. SSCPs (Sammery of safety and clinical performance). Develop, write and update key clinical documentation, including: Literature Search Reports. Clinical Evaluation Reports. Clinical Evaluation Plans (CEP). PMCF Plans and PMCF Reports. SSCPs. Support the clinical evaluation strategy across the medical device portfolio, in close collaboration with Regulatory Affairs and Quality teams. Contribute to Post-Market Surveillance (PMS) activities, including PSURs and PMCF-related documentation. Interact with Notified Bodies and Competent Authorities in relation to clinical documentation and regulatory queries. Ensure all clinical documentation complies with EU MDR 2017/745 , MEDDEV guidance and applicable MDCG documents. DESIRED PROFILE: Scientific or medical background (Biomedical Sciences, Life Sciences, Biotechnology, Pharmacy or similar). Minimum of 3 years of hands-on experience in Clinical Evaluation of medical devices under EU MDR 2017/745 . Proven hands-on experience authoring and updating: CERs CEPs PMCF Plans & Reports SSCPs Solid understanding of: MEDDEV 2.7/1 Rev.4 MDCG guidance Post-market clinical requirements. Experience interacting with Notified Bodies regarding clinical documentation is highly valued. Strong expertise in scientific writing, literature appraisal and systematic literature searches . Familiarity with reference management tools (Zotero, Mendeley or similar). Fluent English and Spanish (written and spoken). WHAT WE OFFER: Permanent and stable contract in a project with high global impact and expanding internationally. Professional and personal development in a vibrant, dynamic, and youthful environment. Competitive salary tailored to your experience, along with an attractive benefits package. Hybrid working model with telework days, and flexible hours. From Monday to Thursday, start between 7:00 and 9:00 a.m. and finish from 4:30 p.m. onwards. On Fridays, enjoy an intensive schedule from 8:00 a.m. to 2:00 p.m. Flexible compensation (meal vouchers, transportation, and childcare assistance). Access to our iWellness program: gym and physiotherapist on site. Corporate events and gifts. Subsidized on-site company cafeteria.

At iVascular , we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of cardio , neuro , and endovascular diseases and to become a reference in the vascular field by enhancing the value of technology and innovation. We are a national company founded in 2010 in Barcelona (Spain) in a phase of growth and international expansion, with subsidiaries already established in Europe, Latin America, Canada, and China, and a team of more than 550 employees covering the entire manufacturing process through vertical integration. We are currently seeking a passionate and experienced Clinical Evaluation Specialist to join our Clinical team at our site in Sant Vicenç dels Horts (Barcelona). You will be responsible for the development a creation of Clinical Documents in accordance the European Medical Device Regulation conducting literature reviews and writing Clinical Evaluation Reports. KEY RESPONSIBILITIES: Development, writing and validation of Clinical Evaluation Reports (CERs) and Clinical Evaluation Plans (CEPs). Execute comprehensive systematic literature reviews , ensuring robust methodology, full traceability and appropriate use of specialized scientific databases. Prepare Literature Seach Reports. Critically appraise clinical evidence (manufacturer-held data and published literature) to support conclusions on device safety and performance in accordance with EU MDR. Review and prepare key clinical MDR documentation, including: CDP (clinical development plan). PMCF-plan (post market clinical follow-plan) PMCF Reports. SSCPs (Sammery of safety and clinical performance). Develop, write and update key clinical documentation, including: Literature Search Reports. Clinical Evaluation Reports. Clinical Evaluation Plans (CEP). PMCF Plans and PMCF Reports. SSCPs. Support the clinical evaluation strategy across the medical device portfolio, in close collaboration with Regulatory Affairs and Quality teams. Contribute to Post-Market Surveillance (PMS) activities, including PSURs and PMCF-related documentation. Interact with Notified Bodies and Competent Authorities in relation to clinical documentation and regulatory queries. Ensure all clinical documentation complies with EU MDR 2017/745 , MEDDEV guidance and applicable MDCG documents. DESIRED PROFILE: Scientific or medical background (Biomedical Sciences, Life Sciences, Biotechnology, Pharmacy or similar). Minimum of 3 years of hands-on experience in Clinical Evaluation of medical devices under EU MDR 2017/745 . Proven hands-on experience authoring and updating: CERs CEPs PMCF Plans & Reports SSCPs Solid understanding of: MEDDEV 2.7/1 Rev.4 MDCG guidance Post-market clinical requirements. Experience interacting with Notified Bodies regarding clinical documentation is highly valued. Strong expertise in scientific writing, literature appraisal and systematic literature searches . Familiarity with reference management tools (Zotero, Mendeley or similar). Fluent English and Spanish (written and spoken). WHAT WE OFFER: Permanent and stable contract in a project with high global impact and expanding internationally. Professional and personal development in a vibrant, dynamic, and youthful environment. Competitive salary tailored to your experience, along with an attractive benefits package. Hybrid working model with telework days, and flexible hours. From Monday to Thursday, start between 7:00 and 9:00 a.m. and finish from 4:30 p.m. onwards. On Fridays, enjoy an intensive schedule from 8:00 a.m. to 2:00 p.m. Flexible compensation (meal vouchers, transportation, and childcare assistance). Access to our iWellness program: gym and physiotherapist on site. Corporate events and gifts. Subsidized on-site company cafeteria.

At iVascular , we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of cardio , neuro , and endovascular diseases and to become a reference in the vascular field by enhancing the value of technology and innovation. We are a national company founded in 2010 in Barcelona (Spain) in a phase of growth and international expansion, with subsidiaries already established in Europe, Latin America, Canada, and China, and a team of more than 550 employees covering the entire manufacturing process through vertical integration. We are currently seeking a passionate and experienced Clinical Evaluation Specialist to join our Clinical team at our site in Sant Vicenç dels Horts (Barcelona). You will be responsible for the development a creation of Clinical Documents in accordance the European Medical Device Regulation conducting literature reviews and writing Clinical Evaluation Reports. KEY RESPONSIBILITIES: Development, writing and validation of Clinical Evaluation Reports (CERs) and Clinical Evaluation Plans (CEPs). Execute comprehensive systematic literature reviews , ensuring robust methodology, full traceability and appropriate use of specialized scientific databases. Prepare Literature Seach Reports. Critically appraise clinical evidence (manufacturer-held data and published literature) to support conclusions on device safety and performance in accordance with EU MDR. Review and prepare key clinical MDR documentation, including: CDP (clinical development plan). PMCF-plan (post market clinical follow-plan) PMCF Reports. SSCPs (Sammery of safety and clinical performance). Develop, write and update key clinical documentation, including: Literature Search Reports. Clinical Evaluation Reports. Clinical Evaluation Plans (CEP). PMCF Plans and PMCF Reports. SSCPs. Support the clinical evaluation strategy across the medical device portfolio, in close collaboration with Regulatory Affairs and Quality teams. Contribute to Post-Market Surveillance (PMS) activities, including PSURs and PMCF-related documentation. Interact with Notified Bodies and Competent Authorities in relation to clinical documentation and regulatory queries. Ensure all clinical documentation complies with EU MDR 2017/745 , MEDDEV guidance and applicable MDCG documents. DESIRED PROFILE: Scientific or medical background (Biomedical Sciences, Life Sciences, Biotechnology, Pharmacy or similar). Minimum of 3 years of hands-on experience in Clinical Evaluation of medical devices under EU MDR 2017/745 . Proven hands-on experience authoring and updating: CERs CEPs PMCF Plans & Reports SSCPs Solid understanding of: MEDDEV 2.7/1 Rev.4 MDCG guidance Post-market clinical requirements. Experience interacting with Notified Bodies regarding clinical documentation is highly valued. Strong expertise in scientific writing, literature appraisal and systematic literature searches . Familiarity with reference management tools (Zotero, Mendeley or similar). Fluent English and Spanish (written and spoken). WHAT WE OFFER: Permanent and stable contract in a project with high global impact and expanding internationally. Professional and personal development in a vibrant, dynamic, and youthful environment. Competitive salary tailored to your experience, along with an attractive benefits package. Hybrid working model with telework days, and flexible hours. From Monday to Thursday, start between 7:00 and 9:00 a.m. and finish from 4:30 p.m. onwards. On Fridays, enjoy an intensive schedule from 8:00 a.m. to 2:00 p.m. Flexible compensation (meal vouchers, transportation, and childcare assistance). Access to our iWellness program: gym and physiotherapist on site. Corporate events and gifts. Subsidized on-site company cafeteria.

At iVascular , we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of cardio , neuro , and endovascular diseases and to become a reference in the vascular field by enhancing the value of technology and innovation. We are a national company founded in 2010 in Barcelona (Spain) in a phase of growth and international expansion, with subsidiaries already established in Europe, Latin America, Canada, and China, and a team of more than 550 employees covering the entire manufacturing process through vertical integration. We are currently seeking a passionate and experienced Head of Clinical Evaluation to join our Clinical team at our site in Sant Vicenç dels Horts (Barcelona). You will oversee the development, writing and supervision of all key clinical documentation, ensuring high-quality systematic literature reviews and the preparation, review and approval of Clinical Evaluation Reports, always in full compliance with the European Medical Device Regulation. Oversee and execute comprehensive systematic literature reviews , ensuring robust methodology, full traceability and the appropriate use of specialized databases. Critically appraise all available clinical evidence —both internal data and published literature—to support well-founded conclusions on device safety and performance. Direct and contribute to the development, writing, validation and approval of Literature Search Reports and Clinical Evaluation Reports (CERs) . High level of English and Spanish. ~Strong expertise writing, literature appraisal and systematic literature searches. ~ Familiarity with reference management tools (Zotero, Mendeley, etc.). Permanent and stable contract in a project with high global impact and expanding internationally. Professional and personal development in a vibrant, dynamic, and youthful environment. Flexible working hours to support a healthy work-life balance.

At iVascular , we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of cardio , neuro , and endovascular diseases and to become a reference in the vascular field by enhancing the value of technology and innovation. We are a national company founded in 2010 in Barcelona (Spain) in a phase of growth and international expansion, with subsidiaries already established in Europe, Latin America, Canada, and China, and a team of more than 550 employees covering the entire manufacturing process through vertical integration. We are currently seeking a passionate and experienced Head of Clinical Evaluation to join our Clinical team at our site in Sant Vicenç dels Horts (Barcelona). You will oversee the development, writing and supervision of all key clinical documentation, ensuring high-quality systematic literature reviews and the preparation, review and approval of Clinical Evaluation Reports, always in full compliance with the European Medical Device Regulation. Oversee and execute comprehensive systematic literature reviews , ensuring robust methodology, full traceability and the appropriate use of specialized databases. Critically appraise all available clinical evidence —both internal data and published literature—to support well-founded conclusions on device safety and performance. Direct and contribute to the development, writing, validation and approval of Literature Search Reports and Clinical Evaluation Reports (CERs) . High level of English and Spanish. ~Strong expertise writing, literature appraisal and systematic literature searches. ~ Familiarity with reference management tools (Zotero, Mendeley, etc.). Permanent and stable contract in a project with high global impact and expanding internationally. Professional and personal development in a vibrant, dynamic, and youthful environment. Flexible working hours to support a healthy work-life balance.

At iVascular , we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of cardio , neuro , and endovascular diseases and to become a reference in the vascular field by enhancing the value of technology and innovation. We are a national company founded in 2010 in Barcelona (Spain) in a phase of growth and international expansion, with subsidiaries already established in Europe, Latin America, Canada, and China, and a team of more than 550 employees covering the entire manufacturing process through vertical integration. We are currently seeking a passionate and experienced Head of Clinical Evaluation to join our Clinical team at our site in Sant Vicenç dels Horts (Barcelona). You will oversee the development, writing and supervision of all key clinical documentation, ensuring high-quality systematic literature reviews and the preparation, review and approval of Clinical Evaluation Reports, always in full compliance with the European Medical Device Regulation. Oversee and execute comprehensive systematic literature reviews , ensuring robust methodology, full traceability and the appropriate use of specialized databases. Critically appraise all available clinical evidence —both internal data and published literature—to support well-founded conclusions on device safety and performance. Direct and contribute to the development, writing, validation and approval of Literature Search Reports and Clinical Evaluation Reports (CERs) . High level of English and Spanish. ~Strong expertise writing, literature appraisal and systematic literature searches. ~ Familiarity with reference management tools (Zotero, Mendeley, etc.). Permanent and stable contract in a project with high global impact and expanding internationally. Professional and personal development in a vibrant, dynamic, and youthful environment. Flexible working hours to support a healthy work-life balance.

At iVascular , we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of cardio , neuro , and endovascular diseases and to become a reference in the vascular field by enhancing the value of technology and innovation. We are a national company founded in 2010 in Barcelona (Spain) in a phase of growth and international expansion, with subsidiaries already established in Europe, Latin America, Canada, and China, and a team of more than 550 employees covering the entire manufacturing process through vertical integration. We are currently seeking a passionate and experienced Head of Clinical Evaluation to join our Clinical team at our site in Sant Vicenç dels Horts (Barcelona). You will oversee the development, writing and supervision of all key clinical documentation, ensuring high-quality systematic literature reviews and the preparation, review and approval of Clinical Evaluation Reports, always in full compliance with the European Medical Device Regulation. Oversee and execute comprehensive systematic literature reviews , ensuring robust methodology, full traceability and the appropriate use of specialized databases. Critically appraise all available clinical evidence —both internal data and published literature—to support well-founded conclusions on device safety and performance. Direct and contribute to the development, writing, validation and approval of Literature Search Reports and Clinical Evaluation Reports (CERs) . High level of English and Spanish. ~Strong expertise writing, literature appraisal and systematic literature searches. ~ Familiarity with reference management tools (Zotero, Mendeley, etc.). Permanent and stable contract in a project with high global impact and expanding internationally. Professional and personal development in a vibrant, dynamic, and youthful environment. Flexible working hours to support a healthy work-life balance.

At iVascular , we are dedicated to the design, manufacturing, production, and commercialization of medical devices for the treatment of cardio , neuro , and endovascular diseases and to become a reference in the vascular field by enhancing the value of technology and innovation. We are a national company founded in 2010 in Barcelona (Spain) in a phase of growth and international expansion, with subsidiaries already established in Europe, Latin America, Canada, and China, and a team of more than 550 employees covering the entire manufacturing process through vertical integration. We are currently seeking a passionate and experienced Product Specialist (Cardio or Endovascular) to join our innovation team at our site in Sant Vicenç dels Horts (Barcelona). Your mission: responsible for the development and implementation of the products under responsibility on a technical/scientific-commercial level. KEY RESPONSIBILITIES: Performing product demonstrations for customers, staff, and other stakeholders Collaborating and strategizing with the MKT, commercial and R+D teams. Working with sales leaders and sales representatives to increase prospects and drive closure of opportunities. Providing training to all sales team members on strategy and product offerings to ensure the effective implementation of product strategies. Identify and report any quality or compliance concerns and take immediate corrective action as required. Providing pricing market knowledge to define market approach strategy. Attending workshops and refresher courses in sales and marketing. Conducting thorough market research, which may include taking surveys, doing desktop research, sending emails and making calls. Planning and assisting with new product releases and events. Scheduling training sessions and attending meetings as required. Identifying new market opportunities and relaying this information to the Manager and other relevant stakeholders. Making helpful product recommendations and suggestions to increase revenue. DESIRED PROFILE: Bachelors Degree in health. Minimum 3 years of selling experience in the medical device market. Articulate and able to perform demonstrations that engage and inspire. Deadline-driven. Superb verbal and written communication skills A strong growth mindset. Spanish and English high level (C1). Excellent organizational skills. Strong presentation skills. Able to travel more 50%. WHAT WE OFFER: Permanent and stable contract in a project with high global impact and expanding internationally. Professional and personal development in a vibrant, dynamic, and youthful environment. Competitive salary tailored to your experience, along with an attractive benefits package. Flexible working hours to support a healthy work-life balance. Flexible compensation (meal vouchers, transportation, and childcare assistance). Access to our iWellness program: gym and physiotherapist on site. Corporate events and gifts. Subsidized on-site company cafeteria.

PLEASE APPLY THROUGH THIS LINK:.Descubra si esta oportunidad es adecuada para usted leyendo toda la información que sigue a continuación.The mission of Speechify is to make sure that reading is never a barrier to learning.Over 50 million people use Speechify’s text-to-speech products to turn wha

We are Socialpoint, a world-renowned mobile game studio proudly part of the Zynga & Take‑Two Interactive family.We’re the creators of hits like Dragon City, Two Dots, Top Troops, and Monster Legends, loved by hundreds of millions of players around the globe.We craft the best social games, bringi

A leading tech company is seeking a Senior Backend Engineer to develop state-of-the-art voice cloning and ensure efficient text-to-speech solutions.Asegúrese de presentar su candidatura con toda la información solicitada, tal como se expone en la descripción del puesto a continuación.The ideal c

Central Localization Program in Barcelona on a hybrid basis or in Montreal Canada.