- What we do
The successful candidate will be joining the QC Analytical team who are responsible for performing chemical and biochemical testing to ensure that the manufactured product is safe, efficacious and fit for patient use as a pharmaceutical material. As a QC Analytical for Porton Biopharma, the post holder will responsible for testing of in process and finished product samples, to defined specifications, while ensuring that work performed within the laboratories is carried out in accordance with the statutory requirements of current GMP and corporate statutory health and safety requirements.
The post holder will be required to work shift rotation. This rotation includes 2 weeks out of 8 weeks where the shift is 2-10pm and potential weekend working (schedule dependent).