This is an exciting opportunity to join a skilled Quality group within the company, reporting to the QC supervisor. The candidate will support the Quality management Systems to achieve targeted compliance, customer-focused, improvements and related site objectives. Responsibilities will include, but not be limited to conducting all general QC testing for raw materials, site water systems, validation and finished goods. Actively utilising SAP for reporting of data, monitoring of results and escalation of OOS results.Culturing of cells for use in testing. Actively participates in the EHS responsibilities for all functions performed within QC, continuous improvement initiatives for QC and root cause analysis evaluation activities as required. This role will be on a 4 on, 4 off shift pattern, working 2 days from 7am-7pm, followed by 2 nights at 7pm-7am and then 4 days off. Who you are:You will have a Bachelors degree preferably in one of the chemical or biological sciences.You will have 1+ years’ experience within the industry working to at least GLP standards but ideally GMP. A Six Sigma/Lean Manufacturing qualification is desirableSampling or cell culturing experience would be beneficialAbility to read and follow verbal instruction.You will be able to follow both written and verbal instruction