Senior R+D Scientist

Skin Tech Pharma Group; Castelló d'Empúries; Presencial; EUR 45.000 - 70.000; Jornada completa

Descripción de la vacante

Une entreprise pionnière dans les dispositifs médicaux injectables recherche un Senior R&D Scientist pour diriger des projets critiques. Cette fonction implique la conception de formulations, le transfert technique et la collaboration avec des équipes multidisciplinaires, visant à respecter des normes élevées de qualité et à répondre aux exigences réglementaires.

Servicios

Environnement stimulant et orienté vers la mission

Impact direct sur des dispositifs injectables innovants

Opportunités d'apprentissage continu

Formación

• Expérience de 10 ans en R&D avec des dispositifs médicaux injectables.
• Expertise en techniques aseptiques, caractérisation rhéologique, montée en propre salle blanche.

Responsabilidades

• Concevoir et optimiser des formulations injectables comme des gels HA.
• Générer des fichiers techniques et gérer le risque (ISO 14971).
• Surveiller les avancées scientifiques et l'activité concurrentielle.

Conocimientos

Aseptique

Analyse Statistique

Rheological Characterisation

Gestion du Temps

Educación

MSc / PhD en Ingénierie Biomédicale, Chimie, Pharmacie ou domaine connexe

Descripción del empleo

With more than 30years of experience in aesthetic medicine, Skin Tech Pharma Group is expanding the frontiers of injectable medical devices that deliver precision, safety, and exceptional patient outcomes. Our portfolio spans visco‑elastic hyaluronic‑acid fillers, collagen stimulators, and novel sustained‑release delivery platforms. To accelerate this growth, we are seeking a SeniorR&D Scientist who will transform visionary ideas into best‑in‑class injectable products.

Your Mission

As our SeniorR&D Scientist, you will lead critical projects from concept through design transfer, closing technical gaps and compressing timelines. You will partner closely with cross‑functional teams to ensure every device we launch meets the highest standards of ISO13485 , EUMDR2017 / 745 , and global market requirements.

Key Responsibilities

• Formulation & Process Development – Design and optimise injectable formulations (e.g., HA gels, microsphere suspensions, depot systems) with a focus on rheology, sterility assurance, and syringe / needle compatibility.
• Scale‑Up & Tech Transfer – Define critical process parameters (CPPs), author process‑validation protocols, and partner with Manufacturing to bring products from lab to GMPclean‑room production.
• Regulatory & Documentation – Generate technical files, risk management (ISO14971), and design history files compliant with MDR and FDA 21CFR820.
• Supplier & Technology Scouting – Identify novel excipients, delivery technologies, and device components that enhance safety and clinical value.
• Mentorship & Collaboration – Guide junior scientists and serve as scientific liaison for Clinical, Regulatory, and Marketing colleagues.
• Trend Surveillance – Monitor scientific advances and competitive activity in injectable aesthetics, drug‑device combinations, and regenerative medicine.

Qualifications

• MSc / PhD in Biomedical Engineering, Chemistry, Pharmacy, Biomaterials Science, or related field.
• 10years hands‑on R&D experience with injectable medical devices or parenteral drug‑device combinations.
• Proven expertise in aseptic techniques, rheological characterisation, and clean‑room scale‑up.
• In‑depth knowledge of ISO13485 , ISO14971 , EUMDR , and relevant FDA guidance for classIII devices.
• Strong analytical skills with proficiency in Design of Experiments (DoE) and statistical analysis.
• Fluent in English and Spanish; excellent technical writing and presentation abilities.

Key Soft Skills

Problem‑SolvingMindset

• Time&PriorityManagement
• Curiosity&LearningAgility

What We Offer

• A purpose‑driven environment where scientific rigour meets creative exploration.
• Direct impact on pioneering injectable devices that elevate aesthetic and therapeutic outcomes.
• A close‑knit, multidisciplinary team committed to mutual respect, continuous learning, and shared success.
• Opportunities to expand your expertise in regulatory strategy, biomaterials, and advanced manufacturing.

If you are excited about shaping the future of injectable medical devices, please send your CV and a 200‑word cover letter to , CC . We look forward to meeting you!