About this role
Role Overview
- Manage and oversee Stability trials within the Medical Propellants Quality Control laboratory
- Compile regulatory evidence for compliance of stability of medical products manufactured by Orbia
- Follow stability master schedule to coordinate on-going and new stability trials for all Medical propellants
- Completing stability reports according to defined timelines
- Raise, report and complete investigations or deviations covering stability studies
- Oversee the maintenance of stability chambers holding stability studies within the medical propellants laboratory
- Support analytical and quality control activities where required
Requirements
- A-Levels essential
- NVQ or above would be desirable
- Experience of working in a QC Laboratory, preferably one working to cGMP standards
- Knowledge and experience in GC analysis
- Experience in stability testing and report writing
- Understanding of stability trials and their role in pharma
- High attention to detail
Benefits
- Development opportunities
- Work-life balance
- Inclusive culture
- Health benefits