ppWhether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else. At Galderma, we actively give our teams reasons to believe in our 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. We have established a Global Capability Center in Barcelona to support Galderma’s growth trajectory and our global commercial and functional teams. Located in the upscale Eixample district in the heart of the city, it offers the possibility for professional career development through exposure to integral and cross‑functional projects. /ppGlobal ESO Quality Specialist (Fixed Term 1‑Year) Primary Location: Uppsala, Sweden Additional Locations: Alby, France | Barcelona, Spain At Galderma, we advance dermatology for every skin story. We are now looking for a dynamic and experienced QA Specialist to join our External Supplier Organization (ESO) for Sterile Products. 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. /ppThe 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. /ph3Key Responsibilities /h3ulliQuality 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. /liliRelease Activities: Execute product release activities in compliance with regulatory requirements and company standards. Ensure the timely and accurate release of pharmaceutical products for distribution. /liliSterile Production: Provide QA oversight for sterile manufacturing operations,



including aseptic processing, sterilization processes, and environmental monitoring. Ensure adherence to cGMP guidelines, regulatory standards, and applicable ISO requirements. /liliDocumentation Management: 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. /liliRegulatory Compliance: Stay up to date with regulatory requirements and industry best practices related to quality assurance. Ensure ongoing compliance with FDA regulations, applicable ISO standards, MDR requirements, and company policies. /liliContinuous Improvement: Identify opportunities for process improvement and quality enhancement. Participate in quality improvement initiatives and projects aimed at optimizing quality systems and operational efficiency. /li /ulh3Required Qualifications /h3ulliBachelor’s degree in Pharmacy, Chemistry, Biology, or a related field. /lili2–5 years of experience in a Quality Assurance role within the medical device, pharmaceutical, or other regulated industry. /liliFluency in written and spoken English; additional languages are considered an advantage. /liliStrong operational knowledge of medical device or pharmaceutical manufacturing processes, including the production of sterile biological drugs, terminally sterilized products, and/or aseptically filled products. /liliProficiency in documentation management. /liliFamiliarity with regulatory requirements, including cGMP, FDA regulations, ISO 13485, MDR, and international guidelines. /liliExcellent communication skills. /liliAbility to work independently and collaboratively in a dynamic, fast‑paced environment. /li /ulh3Preferred Qualifications /h3ulliPharmacist degree or a Master’s degree in Biology, Biotechnology, Biochemistry, Chemistry, Engineering, Microbiology, Life Sciences, or another relevant scientific or engineering discipline. /liliStrong problem‑solving and decision‑making skills.



/li /ulh3What We Offer in Return /h3pYou will be working for an organization that embraces diversity and inclusion and believes that better outcomes are achieved by reflecting the perspectives of our diverse customer base. 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. Our teams are based in modern offices across Europe, including Uppsala (Sweden), Alby (France), and Barcelona (Spain). As you will be working closely with suppliers located across the globe, travel is an integral part of the position. /ph3Who You Are /h3pYou 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. Your expertise and engagement will contribute significantly to Galderma’s continued growth and success. /ph3Our People Make a Difference /h3pAt Galderma, you’ll work with people who are like you—and people who are different. We value what every member of our team brings. 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. 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. /ppFor more information go to /p /p #J-18808-Ljbffr

📌 Global ESO Quality Specialist (Barcelona)
🏢 Galderma Pharma
📍 Barcelona