I am currently supporting our client with the recruitment of a Quality Manager. Our client are a clinical stage biopharmaceutical company who develop immunotherapeutic products and vaccines for the prevention of infectious diseases and cancer.
Responsibilities of the role:-
- You will be responsible for overseeing GCP compliance within the clinical, laboratory and manufacturing group and support the Quality Director in the management of the QMS systems including SOPs, Deviations, CAPA, Change Control, Audits and Risk Assessment.
- You will provide GCP quality expertise and support project teams within the business ensuring best practice are communicated and implemented across the company to ensure that all products are inspection ready at all times.
- You will have strong knowledge of GCP practices, have a degree in a Biologic Science subject and be willing to work from site at least 3 days per week.
Interviews for this role are imminent so please contact Natalie Hough or apply for this role to be considered.