Global ESO Quality Specialist – Sterile Products

Galderma Pharma S.A; Uppsala kommun; On-site; SEK 600,000 - 800,000; Full time

Job summary

Galderma is seeking a Global ESO Quality Specialist to join the External Supplier Organization for Sterile Products in Uppsala, Sweden. The role focuses on QA activities across complaint management, release, sterile production, and documentation within a global, regulated environment.

Ideal candidates have 2–5 years in QA within medical/pharma sectors, strong cGMP knowledge, and excellent communication. Fluency in English is required; additional languages are a plus.

Qualifications

• Bachelor’s degree in Pharmacy, Chemistry, Biology, or related field.
• 2–5 years of experience in a Quality Assurance role within regulated industries.
• Fluency in written and spoken English.
• Strong operational knowledge of medical device or pharmaceutical manufacturing processes, including sterile products.
• Proficiency in documentation management.
• Familiarity with cGMP, FDA regulations, ISO 13485, MDR, and international guidelines.
• Excellent communication skills.
• Ability to work independently and collaboratively in a dynamic environment.

Responsibilities

• Contribute to Quality Systems development and maintenance (deviation, change control, CAPA, risk management).
• Execute product release activities in compliance with regulatory requirements.
• Provide QA oversight for sterile manufacturing operations, including aseptic processing and environmental monitoring.
• Manage and review quality documentation (batch records, SOPs, reports).
• Ensure compliance with regulatory requirements including ISO 13485 and MDR.
• Identify opportunities for process improvement and quality enhancements.

Skills

Quality Assurance

Regulatory compliance

Documentation management

cGMP knowledge

ISO 13485 / MDR

English proficiency

Communication skills

Education

Bachelor’s degree (Pharma/Chem/Bio)

Pharmacist degree (preferred)

Master’s degree in Bio/Ci/Engineering (preferred)

Job description

Galderma is seeking a Global ESO Quality Specialist to join the External Supplier Organization for Sterile Products in Uppsala, Sweden. The role focuses on QA activities across complaint management, release, sterile production, and documentation within a global, regulated environment.

Ideal candidates have 2–5 years in QA within medical/pharma sectors, strong cGMP knowledge, and excellent communication. Fluency in English is required; additional languages are a plus.