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.

Further supporting our growth and innovation momentum, we are establishing a new Global Capability Center in Barcelona to deploy new capabilities to effectively support its global commercial and functional teams. Located in the upscale Eixample District in the heart of Barcelona, Galderma's Global Capability Center offers numerous possibilities for professional development such as exposure to global and cross-functional projects and access to global career opportunities. We are currently seeking a dynamic and experienced Quality Assurance (QA) Specialist with 3-8 years of experience in the medical device or pharmaceutical industry.

The ideal candidate will have expertise in various QA functions, including complaint management, release activities, sterile production, documentation and regulatory compliance.

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.

Sterile Production: Provide QA oversight for sterile manufacturing operations, including aseptic processing, sterilization processes, and environmental monitoring.

Documentation Management:



Manage and review quality documentation, including batch records, standard operating procedures (SOPs), risk management, validation protocols, and reports. Ensure documentation complies with regulatory requirements, ISO13485, MDR and internal quality standards.

Regulatory Compliance: Stay abreast of 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 to optimize quality systems and operational efficiency.

Bachelor's degree in Pharmacy, Chemistry, Biology, or related field. ~5-8 years of experience in a quality assurance role within the medical device, pharmaceutical or regulated industry. ~ Fluency in written and verbal English, any other language is an asset. ~ Strong operational knowledge of medical device or pharmaceutical manufacturing processes, including production of sterile biological drugs, terminally sterilized and/or aseptically filled products. ~ Pharmacist or Master's degree in Biology, Biotechnology, Biochemistry, Chemistry, Engineering, Microbiology, Life Science or another relevant scientific or engineering discipline. Previous experience in reviewing supply agreements and manage quality agreements In ESO organization nearly 60 employees work together in a general environment on our world leading brands such as Nemluvio and Sculptra. We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged.

Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

📌 Quality Specialist - Training (Barcelona)
🏢 Galderma
📍 Barcelona