QA Advisor; GLP

• Location Newmarket Road,Fordham UK, CB75WW
  ,United Kingdom
• Employee Type Regular Full Time

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 growin g 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.

As a QA Advisor , you’ll play a key role in ensuring the quality and integrity of data supporting our GLP a nd GCP studies, while also helping drive continuous improvement across the organi s ation . 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

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

Joining Resolian means becoming part of a global organisation that values collaboration, innovation and continuous improvement. You'll work alongside experienced colleagues, contribute to key quality assurance initiatives and help ensure the integrity and compliance of studies that support scientific advancement.

We encourage professional development, recognise achievement and provide opportunities to grow your career within a supportive and collaborative environme nt. Alongside this, we also offer a range of employee benefits designed to support your wellbeing, career growth and work-life balance.

This is a full-time role based at our site in Fordham, with some opportunity to work flexibly.