Preclinical Principal Scientist at Galderma

Job Description:

Latest job information from Galderma for the position of Preclinical Principal Scientist. If the Preclinical Principal Scientist vacancy in Uppsala län matches your qualifications, please submit your latest application or CV directly through the updated Jobkos job portal.

Please note that applying for a job may not always be easy, as new candidates must meet certain qualifications and requirements set by the company. We hope the career opportunity at Galderma for the position of Preclinical Principal Scientist below matches your qualifications.

Overview

Preclinical Principal Scientist - Injectable Medical Devices Uppsala, Sweden | Hybrid | Full-time | Permanent

At Galderma, we are a global leader in the science of skin. Our Uppsala site is the Global Center of Excellence for Aesthetics, home to over 600 professionals across R&D, manufacturing, clinical development, and marketing. You’ll be part of a multidisciplinary team working with world-leading brands such as Restylane, Azzalure, and Sculptra.

We offer a hybrid work model, continuous learning and career development opportunities, a diverse and collaborative culture, and a modern workplace close to Uppsala Central Station.

As Preclinical Principal Scientist, you will lead the preclinical safety strategy for our next-generation injectable medical devices, from biocompatibility and toxicological risk assessments to supporting regulatory submissions and clinical trials. You will collaborate cross-functionally with R&D, Regulatory Affairs, Quality Assurance, and Clinical Development, as well as with CROs, academic partners, and global regulatory authorities. This is a strategic, science-driven role where your expertise will influence product safety, performance, and success in global markets.

• Define biological risks and shape preclinical strategy for injectable medical devices
• Design, coordinate and interpret preclinical safety and biocompatibility studies
• Ensure compliance with ISO 10993 series, FDA guidance, EU MDR and global regulations
• Write, 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 collaborations
• Contribute to risk assessments per ISO 14971 and biological evaluations per ISO 10993-1
• Monitor scientific and regulatory developments in biomaterials and injectables

• Ph.D. (or equivalent) in Biomedical Sciences, Toxicology, Pharmacology, Bioengineering or similar
• 6-10 years of experience in preclinical development of medical devices, preferably injectables
• Proven expertise in ISO 10993, GLP, EU MDR, and FDA regulatory requirements
• Strong background in biocompatibility testing and toxicological risk assessment
• Experience managing CROs and outsourced preclinical studies
• Excellent scientific writing and communication skills
• Fluent in English (Swedish is a plus)

We are seeking an experienced scientific leader who thrives at the intersection of regulatory science, toxicology, and medical device development.

• A hybrid work model with flexible hours
• Continuous learning & career development opportunities
• A diverse, inclusive, and collaborative culture
• A modern workplace just 10 minutes from Uppsala Central Station

Ready to make a real-world impact? Apply now and take the lead in driving scientific excellence and patient safety in dermatology. Bring your science. Shape the future.

Job Info:

• Company: Galderma
• Position: Preclinical Principal Scientist
• Work Location: Uppsala län
• Country: SE

How to Submit an Application:

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