Quality Assurance Associate

Liverpool Temporary
  • Fantastic opportunity to join a market leading biopharmaceutical company
  • Join a dynamic, innovative and collaborative team.

About Our Client

The client is a market leading Biopharmaceutical company who focus on innovation, integrity and collaboration. With over a century of experience in vaccines, this company has expanded into more than 20 countries with patient focus at the forefront of their efforts.

Job Description

The key roles and responsibilities include:

  • QA frontline support, ensuring and facilitating cGMP behaviours.
  • Project participation, working and collaborating with the QA team to author, review and approve associated cGMP/EHS documentation.
  • Deviation/CAPA and Quality system support, supporting investigations, effective root cause analysis and assessment of corrective actions.
  • Promoting culture in the team and across the site, work in alignment with company values and ensuring HSE measures are applied in the team.
  • Training, both independent training for your own role and maintaining training records.

The Successful Applicant

  • Graduate in relevant discipline, or able to demonstrate capabilities to this level.
  • Understand cGMP requirements and process knowledge
  • Experience in pharmaceutical environment
  • Experience of QMS.
  • Good communication skills
  • Prioritization of data across multiple information sources
  • Team member, happy to work in a team but also willing to work independently

What's on Offer

This is an exciting opportunity to join a market leader in Biopharmaceuticals as one of the Quality Assurance Associates. With patient focus at the forefront of the clients work, your work will help in the preservation of the human population by combating biological disease. This temporary role also comes with a competitive package.

Alex Henman
Quote job ref
Phone number
+44 172 773 0105

Job summary

Contract type
Consultant name
Alex Henman
Consultant phone
+44 172 773 0105
Job reference