Quality Information Specialist, Espoo – Pharmaceutical Quality Systems
18.2.2026https://duunitori.fi/tyopaikat/tyo/quality-information-specialist-sasbe-20002198
Apply by: 2 March 2026
Quality Information Specialist – Pharmaceutical Quality Systems
Orion Corporation is seeking a Quality Information Specialist to join its global quality organization in Espoo, Finland. The role focuses on managing and developing quality information processes and documentation within a regulated pharmaceutical environment.
Key responsibilities include maintaining and improving quality management system (QMS) documentation, coordinating change control processes, supporting audits and inspections, ensuring data integrity, and contributing to continuous improvement of quality processes. The specialist works cross-functionally with manufacturing, regulatory affairs, and R&D to ensure compliance with GMP and internal standards.
Candidates should hold a relevant degree (e.g., pharmacy, life sciences, or related field) and have experience in pharmaceutical quality systems, documentation control, or regulatory compliance. Strong organizational skills, attention to detail, and ability to work in a structured, regulated environment are essential. Familiarity with GMP requirements and electronic quality systems is advantageous.
The position offers an opportunity to work in an international pharmaceutical company committed to high quality standards and continuous development.