Preclinical Principal Scientist

Preclinical Principal Scientist - Injectable Medical Devices📍 Uppsala, Sweden | Hybrid | Full-time | Permanent Shape the future of aesthetic innovation at GaldermaAt Galderma, we're not just offering a job - we're inviting you to shape the future of dermatology. As a global leader in the science of skin, we combine purpose with innovation to improve the lives of millions.Now, we're looking for a passionate and driven Preclinical Principal Scientist to join our team in Uppsala and lead the preclinical safety strategy for our next-generation injectable medical devices. If you're ready to bring science to life and make an impact beyond the lab, this is your chance. Why join Galderma in Uppsala?Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics, home to over 600 professionals working across R&D, manufacturing, clinical development, and marketing - all under one roof.You'll be part of a multidisciplinary team where science meets application, with world-leading brands such as Restylane®, Azzalure®, and Sculptra®. We offer:A hybrid work model with flexible hoursContinuous learning & career development opportunitiesA diverse, inclusive, and collaborative cultureA modern workplace just 10 minutes from Uppsala Central Station About the roleAs Preclinical Principal Scientist, you'll be a key scientific leader responsible for defining and driving preclinical strategies for our injectable devices - from biocompatibility and toxicological risk assessments to supporting regulatory submissions and clinical trials.You'll collaborate cross-functionally with R&D, Regulatory Affairs, Quality Assurance, and Clinical Development, while also working closely with CROs, academic partners, and global regulatory authorities.This is a strategic, science-driven position where your deep expertise will directly influence product safety, performance, and success in global markets. Your main responsibilitiesDefine biological risks and shape preclinical strategy for injectable medical devicesDesign, coordinate and interpret preclinical safety and biocompatibility studiesEnsure compliance with ISO 10993 series, FDA guidance, EU MDR and global regulationsWrite, review, and deliver high-quality scientific documentation: protocols, reports, and regulatory submissions (e.g., IDE, 510(k), CE marking)Act as preclinical lead in cross-functional projects and external collaborationsContribute to risk assessments per ISO 14971 and biological evaluations per ISO 10993-1Monitor scientific and regulatory developments in biomaterials and injectables What we're looking forWe're seeking an experienced scientific leader who thrives at the intersection of regulatory science, toxicology, and medical device development.Must-have qualifications:Ph.D. (or equivalent) in Biomedical Sciences, Toxicology, Pharmacology, Bioengineering or similar6-10 years of experience in preclinical development of medical devices, preferably injectablesProven expertise in ISO 10993, GLP, EU MDR, and FDA regulatory requirementsStrong background in biocompatibility testing and toxicological risk assessmentExperience managing CROs and outsourced preclinical studiesExcellent scientific writing and communication skillsFluent in English (Swedish is a plus) Ready to make a real-world impact?Apply now and take the lead in driving scientific excellence and patient safety in one of the world's most exciting areas of dermatology.🧬 Bring your science. Shape the future.