**Job Description Summary**: The Chem. #3 Quality Control Department, Oslo Site, consists of 19 employees with different background within chemical analysis and GMP Compliance. The department is responsible for the in
- process and release analysis of the aseptic products, establishment of testing regime for new raw materials related to the NPIs, stability, reference standards and the related compliance within QC Chemistry area at the Oslo Site.
QC Chemistry #3 is one of 6 QC Departments organized within the QO area.
As the company is currently growing and developing QC is looking to improve and strengthen the project team within the QC Chem. organization.
**Roles and Responsibilities**
- Responsible for coordination, implementation, and reporting of post approval/ annual/ follow up stability testing.
- Responsible for writing/ updating SOPs, protocols, reports related to stability testing.
- Responsible for change controls, deviations and CAPAs related to stabilit...