Global ESO Quality Specialist

Galderma

Quality Assurance Specialist at Galderma focusing on quality systems and compliance in sterile product manufacturing. Collaborating globally to ensure high standards of quality.

Posted 7/18/2026full-timeUppsala • 🇸🇪 SwedenJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Quality Assurance processes, including complaint management, deviation management, and regulatory compliance in the pharmaceutical and medical device industries. Proficient in documentation management and maintaining quality systems to ensure adherence to cGMP and FDA regulations.

Highest-signal resume keywords

Quality Assurance ExperienceRegulatory Compliance KnowledgeDocumentation Management ProficiencyAseptic Processing OversightProcess Improvement Identification

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Quality Systems DevelopmentComplaint ManagementDeviation ManagementChange ControlCAPARisk ManagementBatch Record ReviewStandard Operating Procedures (SOPs)Validation ProtocolsEnvironmental Monitoring

Soft Skills

Excellent Communication SkillsAbility to Work IndependentlyCollaborative Teamwork

Industry Keywords

CGMPFDA RegulationsISO 13485MDRSterile ManufacturingPharmaceutical ManufacturingMedical Device IndustryRegulated IndustryQuality DocumentationProcess Improvement

About the role

Key responsibilities & impact

Contribute to the development, implementation, and maintenance of robust quality systems, including complaint management, deviation management, change control, CAPA, and risk management processes.
Execute product release activities in compliance with regulatory requirements and company standards.
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.
Stay up to date with regulatory requirements and industry best practices related to quality assurance.
Identify opportunities for process improvement and quality enhancement.

Requirements

What you’ll need

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.
Proficiency in documentation management.
Familiarity with regulatory requirements, including cGMP, FDA regulations, ISO 13485, MDR, and international guidelines.
Excellent communication skills.
Ability to work independently and collaboratively in a dynamic, fast-paced environment.

Benefits

Comp & perks

opportunity to work in an exciting international setting where both professional and personal development are encouraged
working for an organization that embraces diversity and inclusion