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We’re looking for an engineer to help bring small, complex electromechanical products from concept to production. You will join a team that is driving innovation and pushing the boundaries of next-generation EV technology. What you’ll do • Design and develop compact products integrating mechanics, hardware, and software., • Use simulations, prototypes, and testing to validate designs., • Ensure compliance, certification, and smooth handover to manufacturing., • Collaborate with cross-functional teams while driving cost, quality, and timelines. What you bring • Degree in Mechatronics, Electronics, or Mechanical Engineering., • 4+ years developing electromechanical products from concept to production., • Hands-on skills in CAD design, simulations, electronics, and wireless protocols., • Experience working with suppliers and manufacturing partners., • Experience with 1D simulations of electromechanical devices & model validation Nice to have • Knowledge of low-power devices, PCB design, EMC/RED compliance., • Hands-on project experience (e.g., Formula SAE or similar). Please note that this role is on-site.

Akkar is working with a leading e-mobility company to appoint a Senior Hardware Electronics Engineer. You’ll play a key role in developing cutting-edge PCBAs and electronics that meet the highest standards of performance, quality, and compliance for mass production. Key Responsibilities • Translate high-level product and system requirements into robust electronic architectures and PCBAs for innovative EV platforms or related hardware., • Collaborate cross-functionally with mechanical, firmware, software, and testing teams to deliver high-performance solutions on time and within cost targets., • Own the full lifecycle of electronic board development—from concept, schematic design, and component selection to production-ready hardware., • Lead hardware bring-up, validation, debugging, and optimization activities., • Oversee regulatory compliance, validation, and homologation of electronic systems., • Support manufacturing transition, test planning, and end-of-line validation., • Assist with hands-on testing, vehicle integration, and company-wide electronics support needs. Required Skills & Qualifications • BS or MS in Electrical Engineering, Computer Engineering, or related field., • Strong analytical mindset and hands-on problem-solving skills., • Proven ability to work both independently and in multidisciplinary teams., • Comfortable in fast-moving, high-tech environments (e.g., startups or R&D-heavy companies)., • Strong attention to detail with a drive for high-quality, reliable products., • Excellent communication skills; fluent English required. Experience Requirements • Minimum of 5 years in developing and launching complex electronics products., • Deep expertise in analog and digital circuit design across multi-layer PCBs., • Familiar with high-density layouts, double-sided boards, and system-level integration., • Experience with multi-PCB systems architecture, ideally in a vehicle or device setting., • Strong understanding of testing methodologies and failure analysis., • Hands-on proficiency with oscilloscopes, soldering, multimeters, etc., • Familiar with compliance design (EMC, RED) and high-volume manufacturing., • Experience with communication protocols like CANbus, SPI, I2C, and Bluetooth 5. Bonus Skills (Nice to Have) • Direct experience in Battery Management Systems (BMS), ECUs/VCUs, or power electronics., • Confidence in embedded firmware development., • Background in microelectronics or MEMS devices., • Familiarity with business and product development principles., • Involvement in Formula SAE, student engineering teams, or similar.

¡En Sagalés ampliamos equipo! Estamos buscando un/a operador/a de transporte de línea regular para estar en nuestra sala de control operacional, en el sistema de ayuda a la explotación (SAE) ubicada en Valldoriolf. Eres nuestro/a compañero/a ideal si dispones de las siguientes competencias: • Buena actitud, • Flexibilidad y con capacidad de adaptación a entorno dinámico, • Cooperatividad y trabajo en equipo, • Resolución, • Proactividad, • Capacidad de comunicación Responsabilidades que asumirías • Revisión y configuración de la funcionalidad de los equipos, • Revisión recalado Bus-líneas, • Control de la puntualidad al inicio del servicio, • Monitorización del servicio, • Regularización del servicio, • Gestión de incidencias en tiempo real de los servicios, • Comunicación de incidencias al cliente, • Comunicación de incidencias al usuario, • Gestionar y optimizar los medios técnicos y materiales disponibles per a la realización de los servicios. Requisitos: • Formación mínima de CFGS o grado universitario, • Valorable formación en transporte y movilidad, • Valoraremos positivamente que cuentes con experiencia previa en posiciones similares, • Disponibilidad horaria: turnos de mañana y tarde, • Disponibilidad para trabajar 1-2 fines de semana al mes en modo guardia Ventajas de trabajar en Sagalés: • Contratación indefinida e incorporación inmediata., • Jornada completa, • Descuentos especiales por pertenecer al grupo de empresa Sagalés

Medical Monitor, Dermatology, Poland or Spain About The Position The Medical Monitor Dermatology provides medical and scientific support to clinical research programs. The Medical Monitor will perform thorough data review to ensure data integrity and subject safety oversight, and will communicate with sites, investigators, and internal project team members to ensure questions are promptly addressed. This role will be perfect for you if : • You are skilled in building positive working relationships with all stakeholders (clinical sites, colleagues, sponsors) in a clinical research project., • You skillfully balance the strict requirements of clinical research protocols with the realities of clinical trials. Protocols and projects More specifically, as required by the projects’ scope of work, the Medical Monitor will : • Keep current on study protocol, study protocol amendments, Investigator’s Brochure (IB), additional safety information made available during the course of the study, and relevant clinical research guidelines involving the therapeutic indication., • Develop or review Medical Monitoring plan., • Provide project team training on study protocol and / or therapeutic area / indication., • Prepare for, attend, and present at Investigators’ Meetings., • Prepare for and attend Safety Review Meetings, as needed., • Provide 24-hour, 7 days a week, on-call (outside business hours) service for urgent safety-related matters., • Provide ongoing medical support during the study to investigators, site personnel, and monitors., • Provide advice to the sites on protocol-related issues including : questions related to the protocol inclusion and exclusion criteria, concomitant medications / medical conditions, follow-up visits due and guidance on prohibited medication., • Review lab critical values and alerts., • Assess the impact of any prohibited medication taken on study and evaluate any appropriate action for the subject., • Evaluate the appropriateness of any dropout subject replacement., • Provides 24-hour, 7 days a week, on-call service for urgent trial-related safety issues, questions on the protocol, or other safety concerns., • Provides first line contact for investigators, site personnel, and monitors regarding study related medical / safety issues and resolution of study protocol and subject eligibility issues., • Provides advice to the clinical team staff / sites to answer any medical questions related to patient eligibility, and safety or clinical issues during the trial., • Assesses the impact of any prohibited medication taken on study and evaluates any appropriate action for the subject., • Provide project-related medical consultation to the Innovaderm project team members during business hours throughout the duration of the study., • Escalate to the Project Manager or Sponsor any issues requiring medical input and significant safety or data integrity concerns identified during review of data or site contact., • Attend meetings with Innovaderm project team members (PM, DM, stats, CRO) and / or Sponsor, as required., • Verify the medical accuracy of subject safety data and maintain an ongoing assessment of the safety profile of the study., • Review subject safety-related data listings / tools for the purpose of identifying potential trends, unreported protocol deviations related to safety assessments, AEs, and SAEs; and address safety concerns., • Review protocol deviation listings to address potential safety concerns; perform impact assessment; and identify any potential trends., • Review coding listings of adverse events, medical history, and concomitant medications to ensure all terms are coded properly., • Assess if any stopping rule was met and evaluate any appropriate action or follow up with the subject, if applicable., • Review clinical study report., • Provide medical review of SAE form, and reviews SAE causality assigned by the Investigator., • Write and / or review SAE narratives., • Work with the Pharmacovigilance Services provider or Marketing Authorization Holder (MAH) to review SAEs and follow-up on outstanding safety queries, interact with Sponsor and discuss safety issues with sites, as needed., • Provide assistance in pharmacovigilance activities., • Assist Innovaderm / Sponsor in choosing safety committee members., • Serve as a non-voting member of the safety committee to convene and organize proceedings, as applicable., • Develop operating guidelines in conjunction with committee members and submit these to Sponsor for review., • Support business development activities with proposal development and sales presentations., • Participate in feasibility discussions relating to specific project proposals., • Assist with drafting of standard operating procedures and working practices regarding Medical Monitoring activities. Education Experience • Minimum of 5 years of relevant experience in clinical research in a CRO, pharmaceutical, or biopharmaceutical company (Medical Monitor, Medical affairs, Medical Director, Safety)., • Excellent knowledge of the drug development process., • Ability to work in partnership with a multidisciplinary group of colleagues, including translating concepts into practical approaches and promoting consensus., • Outstanding ability to work independently with minimal supervision, ability to work effectively within a team, and matrix environment., • Ability to organize and work efficiently on several projects, each with specific requirements and / or shifting priorities., • Excellent verbal and written communication skills as well as interpersonal skills., • Client-focused approach to work. At Innovaderm, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities. As a Medical Monitor, you will be eligible for the following perks : • Permanent full-time position., • Home-based position. The successful candidate for this position is given to work remotely anywhere in Spain or Poland. About Innovaderm Innovaderm is a contract research organization (CRO) specialized in dermatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Innovaderm continues to grow and expand in North America and Europe. Innovaderm is committed to providing equitable treatment and equal opportunity to all individuals. As such, Innovaderm will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request. Innovaderm only accepts applicants who can legally work in Spain or Poland. 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