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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 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.

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 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 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 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 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.