You will support the Qualty Systems teams which is involved in support the Supplier Quality Management activities on site, in compliance with cGMP standards.
The successful candidate will have experience in:
- 3+ years Supplier Management within the pharmaceutical/biopharmaceutical industry.
- In depth knowledge of GMPs, Goods Documentations and qualification requirements for suppliers
- Experience in reviewing and approving documents
- Able to work independently and effectively in a fast paced environment.
- Experience and knowledge of Quality Management system tools, continuous improvement methodologies and site processes.
- Cross functional team work
12 month contract