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. At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world. Integral ESO Quality Specialist (Fixed Term 1-Year)
At Galderma, we advance dermatology for every skin story. This role offers an exciting opportunity to work in a global environment, supporting world-leading brands such as Nemluvio and Sculptra while collaborating closely with external suppliers across the globe. As part of ESO, you will play a critical role in ensuring product quality, regulatory compliance, and the continuous improvement of our quality systems and processes.
We are seeking a Quality Assurance Specialist with 2-5 years of experience within the medical device, pharmaceutical, or other regulated industries. The position is within the External Supplier Organization (ESO) for Sterile Products, and you will work closely with external manufacturing partners and suppliers to ensure the highest standards of quality and compliance throughout the product lifecycle.
Quality Systems
Contribute to the development, implementation, and maintenance of robust quality systems, including complaint management, deviation management, change control, CAPA, and risk management processes. The main responsibility within the Quality Management System (QMS) area will be complaint management.
Provide QA oversight for sterile manufacturing operations, including aseptic processing, sterilization processes, and environmental monitoring. Manage and review quality documentation, including batch records, standard operating procedures (SOPs), risk assessments, validation protocols, and reports.



Ensure documentation complies with regulatory requirements, ISO 13485, MDR, and internal quality standards.
Stay up to date with regulatory requirements and industry best practices related to quality assurance. Identify opportunities for process improvement and quality enhancement. Participate in quality improvement initiatives and projects aimed at optimizing quality systems and operational efficiency.
Bachelor's degree in Pharmacy, Chemistry, Biology, or a related field.
~2-5 years of experience in a Quality Assurance role within the medical device, pharmaceutical, or other regulated industry.
~ Fluency in written and spoken English; additional languages are considered an advantage.
~ Strong operational knowledge of medical device or pharmaceutical manufacturing processes, including the production of sterile biological drugs, terminally sterilized products, and/or aseptically filled products.
~ Pharmacist degree or a Master's degree in Biology, Biotechnology, Biochemistry, Chemistry, Engineering, Microbiology, Life Sciences, or another relevant scientific or engineering discipline.
Within the ESO organization, nearly 60 employees work together in a highly collaborative global environment supporting world-leading brands such as Nemluvio and Sculptra.
We offer the opportunity to work in an exciting international setting where both professional and personal development are encouraged. You are a resilient and quality-focused professional with a strong sense of ownership and accountability. You thrive in an international and collaborative environment, enjoy building relationships with internal and external stakeholders, and have a passion for ensuring compliance, product quality, and continuous improvement.
Professionalism, collaboration, and a friendly, supportive culture create the perfect environment for people to thrive, develop, and excel in what they do.
Join us on this exciting journey and help shape the future of quality within Galderma's global External Supplier Organization.
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📌 Global ESO Quality Specialist (Barcelona)
🏢 Galderma
📍 Barcelona