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Galderma

Preclinical Principal Scientist

Reposted Yesterday
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In-Office
Uppsala
Senior level
In-Office
Uppsala
Senior level
Lead preclinical safety strategy for injectable medical devices, coordinating studies, ensuring compliance with regulations, and producing scientific documentation.
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Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

 

We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

 

At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.

Preclinical Principal Scientist – Injectable Medical Devices

📍 Uppsala, Sweden | Hybrid | Full-time | Permanent

Shape the future of aesthetic innovation at Galderma

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

About the role

As 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 responsibilities

  • 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

What we’re looking for

We’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 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)

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.

Top Skills

Eu Mdr
Fda Regulatory Requirements
Glp
Iso 10993

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