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About
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 (Apply online only) / 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! Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy
About
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 (Apply online only) / 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! Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy
Nice-to-have skills
* Databases
* Edinburgh, Scotland, United Kingdom
Work experience
* QA
Languages
* English
Seniority level
* Seniority level
Entry level
Employment type
* Employment type
Full-time
Job function
* Job function
Quality Assurance
* Industries
Technology, Information and Internet
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