QA Advisor (GLP)
Resolian · Fordham UK, GBR
Are you an experienced Quality Assurance professional with a strong GLP background and a drive to improve quality and compliance? We’re recruting a QA Advisor to join our growing team. This is an excellent opportunity to apply your established expertise within a scientific environment, supporting bioanalytical and regulated GLP/GCP studies that help bring new medicines to patients.
What you’ll be doing
As a QA Advisor, you’ll play a key role in ensuring the quality and integrity of data supporting our GLP and GCP studies, while also helping drive continuous improvement across the organisation. You'll act as a trusted quality partner, promoting compliance, quality and operational excellence across the organisation.
Your responsibilities will include:
- Conducting study, process and facility audits in line with GLP and GCP requirements
- Supporting the continual improvement of our Quality Management System (QMS)
- Working closely with operational teams to promote quality and compliance across the business
- Supporting customer audits, regulatory inspections and sponsor visits
- Identifying opportunities to improve processes and drive operational excellence
- Building effective working relationships with colleagues, customers and external partners
- Keeping up to date with evolving regulatory requirements and industry best practice
Who we’re looking for
You'll have experience working within a GLP-regulated environment and a strong understanding of GLP principles. This is an essential requirement for the role. You’ll also have experience of carrying out study, process and facility audits and a sound working knowledge of quality systems. You’ll be organised and able to manage competing priorities, both while working independently and as part of a team. Strong communication skills, attention to detail and sound judgement will be key to your success in this role.
It would be great, although not essential, if you also had:
- Experience in a bioanalytical laboratory, CRO or pharmaceutical setting
- Experience of GCP (while the role is primarily focused on GLP-regulated activities, you will support some GCP-regulated studies)
- Experience in CSV QA
- A recognised auditor qualification