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Salary Overview:
The QA Associate will be responsible for providing flexible administrative support to the QA team and providing technical expertise in the eQMS (electronic quality document management system) to the wider business.
They will also support the day-to-day activities in the Regulatory Archives assisting with company archiving needs, arranging and co-ordinating collections of material with external providers and the administration of eArchive. Main Responsibilities:
hVIVO is currently seeking a Quality Assurance Associate to join the Quality Assurance (QA) team in London E1. This role is a site based role with limited opportunity to work from home.
The QA Associate will be responsible for providing flexible administrative support to the QA team and providing technical expertise in the eQMS (electronic quality document management system) to the wider business.
They will also support the day-to-day activities in the Regulatory Archives assisting with company archiving needs, arranging and co-ordinating collections of material with external providers and the administration of eArchive.
- Administration of eQMS including user account management, coordination of workflows and query management.
- Day to day support of the hVIVO regulatory archive (paper and electronic) and liaise with offsite archive provider to arrange collections and deliveries. Liaise with clients regarding material reaching retention,
- Administration of CAPA module of eQMS (CAPA workflows and follow up on outstanding actions).
- General administrative support to the QA team.
- Previous administration experience in clinical research (essential)/QA function (desireable) in pharmaceuticals or CRO organisation
- Skilled in use of electronic document management systems
- Hands on, adaptable, pragmatic approach
- Excellent attention to detail
- Problem solver
- Experience in SOP administration
- Science degree
