Terapeuta - Glow Beauty Puerto Banús

Company Description “Our Marbella clinic redefines luxury healthcare, offering exclusive aesthetic medicine and minor surgical treatments in an elegant, private setting. Led by expert physicians , we provide bespoke medical care that blends advanced science with refined comfort and personalized attention.” Role Description This is an on-site role for a Dermatologist at Skin Medical and Aesthetic Clinic located in Marbella. The Dermatologist will be responsible for diagnosing and treating various skin conditions, managing patient consultations, and performing cosmetic dermatological procedures. The Dermatologist will also be expected to provide acne treatments, develop treatment plans, and educate patients about skincare and preventative measures. Qualifications • Proficiency in Dermatology and Cosmetic Dermatology, • Experience in Medicine and Cosmetology, • Ability to effectively address and treat Acne, • Excellent diagnostic and clinical skills, • Strong patient communication and education skills, • Ability to work independently and in a team, • Board certification in Dermatology, • Valid medical license to practice in Marbella

Buscamos Cuidador/a de personas mayores en Marbella y alrededores. Conocimientos previos para desarrollar funciones de Cuidador/a de personas mayores. Solicitudes de nuevos trabajos y clientes en tu zona, que necesitan Cuidador/a de personas mayores.

Eres psicólogo/a y te gustaría trabajar con total flexibilidad, desde donde quieras? Imagina poder organizar tu tiempo, trabajar desde distintos lugares y ofrecer tus servicios de manera moderna y segura.Nuestro cliente te ofrece la oportunidad de unirte a una plataforma online innovadora que es

Position: Medical Device Development Lead Level: Mid - Senior Type : Internal, Full-time Location: Spain (work permit provided for non-EU employees, must be willing to relocate) Job description : This is a full-time role for a Medical Device Development Lead with flexible location based in Spain. The position will offer the opportunity to work with a global cross-functional team, supporting medical device design stage initiatives while gaining exposure to various technologies. The role will involve in-person and/or remote collaboration as needed according to assigned projects. The Medical Device Development Lead will own and contribute to comprehensive design initiatives across the full product life cycle. Main Responsibilities: Drive device development projects across all design stages, collaborating with subject matter experts to complete deliverables following applicable Design Controls. Author key Design History File documents (DIR, Design V&V reports, etc.) and complete phase reviews. Draft applicable Risk Management and Human Factors documentation, improving product design and user interactions (RM Plan, FMEA, URRA, Task/Comparative Analysis, etc.). Ensure that medical device RM and Usability considerations are documented according to applicable standards (e.g., ISO 14971, IEC 62366). Collaborate with manufacturers as technical lead, planning assemblies required for testing, clinical trial, or commercial production. Support Post-Market Surveillance activities and determine necessary updates to product design, Risk File, and Usability based on collected feedback. Support Regulatory Affairs in preparing medical device pre-registration documents (various regions). Provide input to health authority inquiries. Work with common word processing, spreadsheet, and collaborative tools (e.g., Microsoft Office), and present online in video conferences. Candidate profile and required qualifications: Relevant Experience: a minimum of 5 years within the medical device or pharmaceutical industry is required (e.g., developing medical devices, SaMD, combination products, IVDs). Studies: BS, MS, or PhD. in Engineering or health-related field. Experience working with cross-functional teams in medical device development from concept to market launch. Prior experience as a subject matter expert responsible for DHF documentation (e.g. R&D, RM, HFE, QA, RA, Clinical). Self-directed, works independently in a remote setting and as part of a team. Demonstrates excellent interpersonal skills, working with diverse groups of people in a global arena. Ability to drive decisions, promote progress, and manage multiple projects. Offers strategic and practical solutions to development team, presenting findings in concise and clear manner. Familiarity with global regulatory requirements (FDA, CE Marking, ISO 13485, MDR, etc.). Experience with HA submission preparation is a plus. Interested in gaining experience in multiple key roles of medical device development, across various technologies. Experience in medical device software development or connected SW/HW is a plus. Language Requirement: English – Full proficiency reading/writing. If applicable, willing to relocate - flexible location residing in Austria or Spain. What we offer: One of the best overall career opportunities in the sector Rapid learning and development opportunities on a global scale Very competitive salary/bonus 5 weeks vacation + local holidays Optimal work-life balance with a company policy and management approach built for sustainable career satisfaction Health insurance and a culture geared toward health and well-being An amazing collaborative team that is diverse, talented, and ready to celebrate success Fun fact: we come from 7 different countries and 4 continents About our company: Suma Medtec accelerates development projects for medical device and pharmaceutical manufacturers of all sizes. We support all aspects of product development and commercialization, with specialized competencies in Global Regulatory Affairs, Risk Management, Human Factors, Project Management, R&D Engineering, and Quality. For additional information about Suma Medtec, we invite you to visit our website: Suma Medtec GmbH is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We encourage applications from candidates of all backgrounds, experiences, and perspectives. Please note that applications received through third-party staffing or recruiting companies will not be considered.

Senior Toxicologist – Contract (Remote or On-Site, Spain) Location: Spain (Remote or On-Site) Contract Type: Freelance/Contract Experience: 12+ years Overview Our client is initiating a major project in Spain and is seeking an experienced Senior Toxicologist to provide high-level scientific leadership on a contract basis. The ideal consultant will bring deep expertise in toxicology and non-clinical safety, supporting strategic input across complex development activities. Key Responsibilities Lead and advise on non-clinical toxicology strategy across development programs Design, review, and interpret toxicology studies Prepare or contribute to regulatory documentation Support regulatory interactions as needed Collaborate effectively with cross-functional teams Requirements Minimum 12 years’ professional experience in toxicology Strong background in non-clinical safety assessment Proven experience in study design, data interpretation, and strategy Regulatory submission experience highly beneficial Ability to work independently and proactively What We Offer Competitive contract day rate Flexible setup: fully remote or on-site in Spain Opportunity to contribute to a high-visibility international project

Gracias a nuestra plataforma de gestión de clientes, podrás aceptar o descartar solicitudes de trabajos en tu área, enviando presupuestos solo a los clientes que más te interesen. Pertenecer a la red de profesionales de Cronoshare no tiene coste y recibirás nuevos clientes según tus preferenci

Gracias a nuestra plataforma de gestión de clientes, podrás aceptar o descartar solicitudes de trabajos en tu área, enviando presupuestos solo a los clientes que más te interesen. Pertenecer a la red de profesionales de Cronoshare no tiene coste y recibirás nuevos clientes según tus preferenci

Se busca auxiliar de enfermería para un entorno laboral centrado en el bienestar de las personas mayores y dependientes, con un modelo de atención personalizado.