ppDescripción del trabajo At Docplanner Group, we’re on a mission to help people live longer, healthier lives. As the world’s largest healthcare platform, each month, we connect 24 million patients with 280k doctors across 13 countries (through brands like Znany Lekarz, Doctoralia, Mio Dottore, Doktor Takvimi, and jameda). Our marketplaces, Saa S and AI tools simplify daily tasks and help doctors, clinics and hospitals work more efficiently, so they can focus on what really matters: caring for their patients. Learn more about our products here: pro.Doctoralia.Es /p h3Why join us? /h3 pReal impact – We help doctors help patients. Your work truly makes a difference. /p pAt scale, yet agile – 3,000+ employees, but still fast, versátil, and hands‑on. /p pShape the future, sustain growth – Make a difference now and build for long‑term success. /p h3Job Description /h3 pThe Risk Compliance team ensures Docplanner meets regulatory requirements while supporting safe, scalable, and innovative healthcare solutions. As our products increasingly transition into medical device territory, regulatory compliance is a core enabler of our growth, trust and ability to operate globally. /p pWe are hiring a Senior Healthcare Regulatory Specialist (Sa MD) to join our global team. In this role, you will act as the Person Responsible for Regulatory Compliance (PRRC) under EU Medical Device Regulation (MDR), partnering closely with Product, Engineering, Machine Learning and Data, Customer Care and Legal teams to ensure our Software as a Medical Device (Sa MD) products meet regulatory requirements across Europe. You will play a key role in enabling Docplanner to operate safely, compliantly and at scale in an increasingly regulated digital healthcare environment. /p pThis is a new and highly impactful opportunity, where you will help build and strengthen our regulatory framework, directly supporting one of Docplanner’s core strategic priorities: EU MDR compliance and global expansion. You’ll gain exposure to innovative healthtech and AI‑driven products, work with cross‑functional teams across multiple markets. /p h3How will you make an impact? /h3 ul liEU MDR Compliance:



Achieve mandatory Medical Device Regulation certification to maintain European market access. /li liSupport Global Certification Processes: Lead MDR certification and other accreditation (ISO, C5) processes across target jurisdictions to enable market expansion and continuance. /li liEstablish Compliant Governance Framework: Build robust governance systems that stakeholders and customers can trust, ensuring business integrity and regulatory adherence. /li liRisk Mitigation Business Protection: Prevent regulatory fines and reputational harm that could impact our ability to serve patients and healthcare providers. /li liProcess Optimization: Continuously assess and improve compliance processes to align with the dynamic needs of the increasingly regulated digital healthcare industry. /li /ul h3Qualifications /h3 ul liStrong knowledge of EU Medical Device Regulation (MDR), particularly in a Software as a Medical Device (Sa MD) context. /li liPractical experience in medical device regulatory affairs and solid understanding of Quality Management Systems (QMS) and regulatory governance frameworks. /li liRelevant academic background (law, medicine, pharmacy, engineering, or scientific field) or the equivalent hands‑on experience in medical device regulatory/QMS experience. /li liExperience with EUDAMED, CAPA systems, and post‑market surveillance tools. /li liAbility to manage cross‑functional regulatory projects independently and work with multiple stakeholders. /li liStrong communication skills with both internal teams and external regulatory authorities. /li liFluent in English; Spanish or other EU languages are a plus. /li liNice To Have: Knowledge of the EU AI Act. /li liNice To Have: Familiarity with Agile / software development environments. /li /ul h3Additional Information /h3 pPosition: Senior Healthcare Regulatory Specialist (Sa MD) /p pLocation: Spain (remote‑friendly)



/p pContract: Full‑time /p pBenefits: /p ul liHealthcare insurance /li liWellness that works for you – from gym memberships to mental health support, we’ve got you covered. /li liTime off that counts – whether it’s a vacation, your birthday, or just a day to recharge, we believe in balance. /li liESOP (Employee Share Option Plan) after 6 months with us – because we believe in sharing our success! /li liLocal perks – depending on your location, you will be entitled to local benefits like meal vouchers (ticket restaurant), transport allowances, or extended parental leave. /li liCareer Growth – We’re growing, and so can you! You’ll find lots of chances to learn, develop, and explore new paths—whether within your team or through cross‑functional projects. /li liA Truly Global Team – Work with talented people from all over the world in a diverse and inclusive environment. /li /ul h3Flexibility That Works for You /h3 pRemote work and flexible hours aren’t just buzzwords here. While the extent of flexibility depends on your role and team, we value results over rigid schedules. /p pWe welcome you at any of our hubs in Barcelona, Warsaw, Curitiba, Rio de Janeiro, Mexico City, Bogotá, Munich, Rome or Bologna. /p pPlease note: At this time, we are not able to sponsor visas for this position. To apply, you must already have the legal right to work in your country of residence or the location of the role. /p h3What We Believe In /h3 pAt Docplanner, our values guide everything we do: Focus on results – we're here to make an impact. Think like an owner – take responsibility, drive outcomes. Keep it simple, keep it lean – smart solutions over complexity. Be respectful and radically honest – openness builds trust. Learn and be curious – growth is part of the job. /p pWe are committed to building a team that represents a variety of backgrounds, perspectives, and skills. We welcome applicants from all walks of life, regardless of gender, disability, or background, and are dedicated to fostering an inclusive workplace where everyone feels valued and empowered to contribute. /p /p #J-18808-Ljbffr

📌 Senior Healthcare Regulatory Specialist (Samd) - (Remote-Friendly Within Spain)
🏢 Docplanner
📍 Madrid