QA Advisor (GLP)
Resolian · Fordham UK, GBR ·
- Employment
- Full time
- Category
- QA
Resolian is hiring a QA Advisor in Fordham, UK to conduct study, process and facility audits under GLP (with some GCP studies), support and improve the Quality Management System, and assist with customer audits and regulatory inspections in a bioanalytical lab helping bring new medicines to patients.
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