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| Job Location | Slough |
| Education | Not Mentioned |
| Salary | £20.00 - £28.00 per hour |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Contract, full-time |
QA, QC, GLP, GCP, Trackwise Your new companyThe company are an innovative and expanding Global Pharma who are the market leaders within their therapy areas of expertise. Currently they have one of the largest and most exciting pipelines in the current market which contains multiple product launches in the next 12 months and several exciting studies within their Early Phase portfolio. Your new role* Distributing & provisional review of Study Plans and Standard Operating Procedures* Generating process maps of RQ standard procedures, during the update of the SOPs* Drafting QA Statements from information within TrackWise * Formatting of Audit Reports from TrackWise export prior to distribution * Preparation / Coordination of GLP and GCP Lab Refresher training meetings (Outlook)* Assisting with TrackWise entry for some audits (from structured audit notes) (database)* Tracking CAPA and follow up within TrackWise; possible follow up with internal CAPA owners What youll need to succeedAbility to work with multiple systems and multiple spreadsheets simultaneously and be focused about what information is captured in each place and experience with web-based software such as Trackwise. You will also have strong Microsoft skills. Previous experience in QA/QC will be necessary within the Pharmaceutical industry. You will also be educated to a degree level as minimum.What you need to do nowIf youre interested in this role, click apply now to forward an up-to-date copy of your CV, or call us now.If this job isnt quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.