Job Description:
- Working to GMP standards in a busy pharmaceutical manufacturing environment
- Running production lines in compression and granulation
- Creation of Batch Records and SOP Writing
- This role is currently planned on a 2 cycle shift pattern but flexibility is required to work on days or other shifts if required
Skills/Knowledge/Experience:
Previous pharmaceutical manufacturing experience in an FDA regulated environment in the following areas:
- Compression
- Granulation
- Previous experience in creation of Batch Records and SOP writing
- 3rd level qualification in addition to this experience would be desirable
Salary: 30-35k+ and Shift Allowance when applicable (20% on 2 cycle)
