QA Associate

QA Associate

Full-Time 25650 - 31350 Β£ / year (est.) Home office (partial)
hVIVO

At a Glance

  • Tasks: Support the QA team with administrative tasks and manage electronic quality systems.
  • Company: Join hVIVO, a leading company in clinical research based in Canary Wharf.
  • Benefits: Full-time role with competitive salary and opportunities for growth.
  • Other info: Flexible on-site work 2/3 days a week with a focus on detail and problem-solving.
  • Why this job: Be part of a dynamic team making a difference in healthcare.
  • Qualifications: 5 GCSEs and A levels; experience in admin or support roles preferred.

The predicted salary is between 25650 - 31350 Β£ per year.

h VIVO is currently seeking a Quality Assurance Associate to join the Quality Assurance (QA) team in London E14, Canary Wharf. This role is on site 2/3 days a week.

The QA Associate will be responsible for providing flexible administrative support to the QA team and providing technical expertise in the e QMS (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 e Archive.

  • Administration of e QMS including user account management, coordination of workflows and query management.
  • Day to day support of the h VIVO 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 e QMS (CAPA workflows and follow up on outstanding actions).
  • General administrative support to the QA team.

Essential

  • Experience in an admin or support role previously
  • 5 GCSEs Grade C or above, A levels
  • Skilled in use of electronic document management systems
  • Hands on, adaptable, pragmatic approach
  • Excellent attention to detail
  • Problem solver

Desirable

  • Experience in SOP administration
  • Science degree
  • Clinical research experience in pharmaceuticals or CRO organisations
  • Please note this role is full time and permanent and the incumbent must have full working rights in the UK to apply**
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QA Associate employer: hVIVO

hVIVO is an exceptional employer, offering a dynamic work environment in the heart of London where innovation meets healthcare. As a leader in human challenge models, we provide our Study Physicians with unparalleled opportunities for professional growth and development, alongside a supportive culture that values collaboration and excellence. Our commitment to advancing drug and vaccine development ensures that you will be part of meaningful work that has a real impact on public health.

hVIVO

Contact Details:

hVIVO Recruitment Team

We think you need these skills to ace QA Associate

Quality Assurance
eQMS (electronic quality document management system)
Regulatory Archives Management
User Account Management
Workflow Coordination
Query Management
CAPA Administration