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Educación

hace 5 horas•76 vistas

Formador/a de EntrenadoresBarcelona

COBOSU AND TRAINERS POINT SLActivo hace 21 minutos

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Go Software Engineer - Cloud

hace 15 días

Barcelona

About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. Interested in applying your wealth of technical knowledge and experience towards an opportunity in the medical field and improve the lives of people? In our new Technology Hub in Barcelona, you will join our purpose driven team to: • Drive innovation in health tech by developing scalable platforms that transform real-time biosensor data into meaningful insights., • Shape the future of digital health by building solutions that empower people to take control of their metabolic health., • Create engineering with a global impact by working on technology that reaches millions worldwide., • Advance accessibility and compatibility by ensuring our solutions integrate seamlessly across devices and ecosystems. Candidates will work with a modern tech stack on a Software as a Service cloud platform as well as internal and external APIs to improve the health and well-being of users in over 25 countries in a large-scale system responsible for processing billions of messages daily. The candidate should bring passion for software engineering and a desire for continuous learning as well as versatility, leadership qualities and a desire to shape the direction of the team. Candidate will support building scalable, highly available, efficient, and secure cloud solutions for a medical device SaaS. #software Responsibilities • Design and implement services and components utilizing Go for cloud-based platforms., • Collaborate with internal and external partners to develop and integrate with APIs that empower users to share and utilize their medical data in partner systems., • Design and implement unit testable code that are highly maintainable., • Collaborate directly with InfoSec to design and implement secure solutions., • Provide new ideas and insight in collaboration with the data services team., • Ensure performance, uptime, and scale, maintaining high standards of code quality and thoughtful design., • Contribute to significant architectural and operational decisions in collaboration with the Architecture team., • Build out our internal tooling and APIs to make business and engineering processes more efficient., • Implement systemic changes to align existing systems with current architectural goals., • Create diagrams, flowcharts and models that illustrate the internal design and workflow of solution components., • Engage in technical planning, design, and code reviews including peer code reviews., • Collaborate as an enaged member of an agile team, realizing features through development, test, and delivery., • Stay current with emerging trends, making recommendations as needed to help the organization innovate. Required Qualifications • Bachelors Degree in Computer Science, Information Technology or other relevant field., • Software development experience, ideally in Go. A willingness to learn new software development languages to meet goals and objectives., • Strong Computer Science fundamentals and experience with software development., • Understands Object Oriented Programming and design and building modular unit testable code., • Understands the principles of designing, implementing, and maintaining highly complex asynchronous messaging and backend processing jobs., • Understands the concepts of Docker Containers and container orchestration services such as Docker Swarm, ECS, and Kubernetes.., • Experience with Git for source control on a collaborative project., • Comfortable working asynchronously with a distributed team. Preferred Qualifications • Practical experience and understanding of working with and developing RESTful APIs and microservices., • Experience contributing to a scalable architecture/design of existing and new systems that are highly available and easy to maintain and monitor., • Understanding and familiarity of Test Driven Development (TDD)., • Experience working with relational datastores such as SQL Server, Postgresql, or MySql., • Experience working in an agile environment.., • Practical Knowledge of Linux.

Health And Safety Specialist (PRL)

hace 3 días

Barcelona

We are Impress. We believe everyone deserves a smile they love. Our long-term vision is to disrupt European conventional dentistry and orthodontia. Impress is a European direct-to-consumer teeth-aligner and oral care startup. We provide an affordable and convenient way to straighten teeth with aligners treatment. Within the Human Resources department, we are looking for a Health & Safety Specialist. You will be part of a winning team and passionate about what it does. Are you ready to join us? Responsabilities: • Be the point of contact of our sservicio de prevención ajeno in Spain and make sure we comply with all the regulations across all our locations in Spain, • Prepare risk evaluations for our different workplaces, both the office and the clinics, to propose preventive and control measures and risk reduction, • Create prevention plans, politics and procedures, • Adapt our facilities to the current health and safety regulations, • Prepare the needed technical reports and documentation, • Manage inspections, audits and follow-up visits, • Manage the information and training of the employees, • Collaborate in internal health and safety campaigns What you need to be successful: • Master’s Degree in Occupational Risk Prevention, • +2 years’ experience in a similar role in Occupational Risk Prevention, preferably in a similar company, • Knowledge of health and safety legislation, • Spanish and communicative level of English 💡 Why Join Us: • Modern, well-equipped offices with high-end technology., • Special benefits and discounts on company services and products., • Free Gym inside our offices., • Comprehensive training programs for professional growth and leadership development., • Dedicated support team to assist with administrative and operational tasks., • Dynamic, fast-paced environment offering impressive career development opportunities. We cultivate a culture of inclusion and diversity. We celebrate our employees' individual strengths, views, and experiences, and we encourage all candidates to apply, without regard to race, colour, religion, gender identity, sexual orientation, origin, disability, or any other factor. Our differences enable us to be a better team; one that makes better decisions, drives innovation, and delivers better results. Join us today and make a difference, one smile at a time!

Senior Regulatory Affairs Specialist – Clinical Trials (CTIS)

hace 3 días

Barcelona

Are you a Regulatory Affairs professional with solid experience in EU Clinical Trial Regulation (CTR) and submissions via CTIS and AEMPS? At the Barcelonaßeta Brain Research Center (BBRC) – research center of the Pasqual Maragall Foundation – we are looking for a Senior Regulatory Affairs Specialist to lead institutional clinical trial submissions and ensure full regulatory oversight across our research portfolio focused on Alzheimer’s prevention. This role sits within the Clinical Operations Office and acts as the institutional reference for regulatory strategy and compliance. Main responsibilities: Regulatory Strategy & Clinical Trial Submissions • Lead regulatory strategy for institutional clinical trials under EU CTR., • Prepare and submit dossiers via CTIS, AEMPS, and Ethics Committees (CEIm)., • Manage substantial modifications, DSURs, safety notifications, and regulatory updates., • Act as primary contact with competent authorities and regulatory bodies. Sponsor Regulatory Oversight • Ensure compliance with EU CTR, GCP, GDPR, and national regulations., • Support inspection-readiness and regulatory audits., • Contribute to regulatory risk assessment and mitigation strategies. Quality & Institutional Compliance • Develop and maintain SOPs related to regulatory activities and GCP., • Support CAPAs and quality system improvements., • Promote harmonization of regulatory processes across research units. Team & Institutional Support • Supervise and mentor a junior regulatory profile., • Provide internal training on regulatory requirements and updates., • Collaborate closely with scientific and clinical operations teams. Requirements • Degree in Life Sciences (Pharmacy, Biotechnology, Biomedicine, Biology or related field)., • Minimum 3–5 years of experience in Regulatory Affairs within clinical trials involving Investigational Medicinal Products (IMPs) in a clinical research institution or pharmaceutical industry setting., • Demonstrated experience in the preparation and submission of clinical trial applications under the EU Clinical Trial Regulation (EU CTR) via CTIS., • Proven experience interacting directly with AEMPS and Research Ethics Committees (CEIm)., • Solid knowledge of ICH-GCP, EU CTR, and Spanish clinical trial regulatory framework., • Experience managing substantial modifications, safety notifications, and Development Safety Update Reports (DSURs)., • Familiarity with EudraCT, RIMS, and other regulatory platforms., • Advanced level of English and Spanish; Catalan is an asset., • Proficiency in digital tools for document management and regulatory tracking. What we offer • Location: Barcelona, • Contract: Permanent, full-time (38 hours per week), • Salary: Commensurate with experience and aligned with the institutional compensation policy, • Benefits: Flexible benefits scheme including meal vouchers, health insurance and childcare support, • The opportunity to join a leading European research center focused on the prevention of Alzheimer’s disease and related dementias within a scientifically rigorous and collaborative environment.

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