SRG are working with an established CRO to help them find a new QA Officer.
This is a great opportunity for someone looking for a new challenge in the QA field and is looking for a work/life balance as the company offer great benefits such as enhanced holidays and pension.
The Role:
* QA monitoring of studies, on site facilities and where relevant suppliers and subcontractors to ensure compliance with Regulatory Standards
* Scheduling and conduct of audits - suppliers, subcontractors, facility, processes, critical phase, protocol, data and reports
* Review and provide QA approval of Standard Operating Procedures, Study Plans, protocols equipment calibration validation records and supporting documentation
* Maintain the Master Schedule
* Support in training on QA for other members of staff and departments
* Provide advice and guidance for any department on QA and regulatory queries
* Any other QA activities as required
Requirements:
* A degree or equivalent experience in a life science discipline
* Previous experience in a QA/Quality focused role
* A sound knowledge/experience of Good Laboratory Practice (GLP)
* Experience of GLP 3106-1999 / OECD No 1 is essential
* Experience authoring and reviewing/auditing SOPs/study plans and reports
* Experience of equipment calibration would be beneficial
* Experience in quality auditing
* Working knowledge of databases, spreadsheets and other online quality and project management systems
* Strong communication skills and ability to work as part of a busy team
If you meet the above requirements and are looking for a new role, then please apply online to find out more!
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