Engineer, Injectable Platform PMS&T

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.

Engineer, Injectable Platform Technology & NPI

Location: Uppsala, Sweden

At Galderma, we are dedicated to advancing dermatology for every skin story. We are now looking for a talented and motivated Process Engineer / Scientist to join our Injectable Platform Technology & NPI team in Uppsala.

Reporting to the Head of Injectable Platform Technology & NPI , you will play an important role in supporting the introduction, transfer, and commercialization of innovative injectable products. This is an exciting opportunity to work at the intersection of development and manufacturing, collaborating with global cross-functional teams to bring new products from concept to commercial reality.

Key Responsibilities

• In this role you will support the successful transfer of new injectable products from development into commercial manufacturing, while ensuring that the injectable platform standards and best practices are applied. You will contribute to process optimization, validation, technology transfer activities, and manufacturing readiness, ensuring robust and compliant production processes. The role also expands into building, applying and maintaining a platform approach for injectable products, as well as supporting continuous improvement initiatives.
• You will serve as a technical expert for manufacturing processes, supporting internal and external manufacturing sites throughout product launch activities. The role involves preparing and reviewing technical documentation, validation protocols, reports, and regulatory submissions while ensuring compliance with GMP requirements and applicable regulatory and platform standards.
• Working closely with colleagues across Product Science, Manufacturing Science & Technology, Quality, Regulatory Affairs, and external manufacturing partners, you will help address technical challenges, manage risks, support project execution, and drive continuous improvement initiatives. You will also contribute to platform standardization efforts and support the successful delivery of key project milestones.

Qualifications

• Required Qualifications
• Bachelor's or Master's degree in Chemistry, Biochemistry, Biological Sciences, Chemical Engineering, or another relevant scientific or engineering discipline.
• Approximately 2–5 years of experience within the injectable medical device, pharmaceutical, or biopharmaceutical industry.
• Experience with injectable Semi-Finished Product (SFP) and/or Drug Product manufacturing.
• Knowledge of regulatory requirements, ISO standards, and GMP guidelines.
• Strong analytical and problem-solving capabilities with excellent attention to detail.
• Strong communication, documentation, and collaboration skills.
• Fluency in English, both written and spoken.

Preferred Qualifications

• Experience in process validation, technology transfer, commercialization, manufacturing support, and troubleshooting.
• Experience working with contract manufacturing organizations (CMOs) and external stakeholders.
• Experience with device assembly, including autoinjectors, and packaging processes.
• Experience working in GMP and/or ISO-regulated environments.
• Knowledge of quality systems and risk management tools such as deviations, change controls, CAPA, and FMEA.
• Experience driving continuous improvement initiatives using Lean, Six Sigma, or similar methodologies.
• Who You Are
• You are a collaborative and scientifically driven professional who enjoys solving complex technical challenges in a dynamic environment. You thrive in cross-functional teams, communicate effectively with both technical and non-technical stakeholders, and are motivated by delivering high-quality results. With a proactive mindset and a strong sense of ownership, you are eager to contribute to the successful launch and continuous improvement of innovative injectable products.

What We Offer

At Galderma, you will have the opportunity to work in a global organization focused on innovation and patient impact. You will collaborate with experienced colleagues across multiple functions and play a key role in bringing new products to market while developing your technical and professional expertise in a highly regulated and scientifically advanced environment.

Ready to make an impact? We look forward to hearing from you.