GCP QA Consultant (Contract)

Your new company You will be supporting an innovative UK-based biotech entering first-in-human studies, backed by strong funding and progressing a novel therapeutic pipeline into early clinical development. The organisation is at a pivotal stage, building out its clinical and quality infrastructure as it transitions toward the clinic. Your new role As a GxP QA Consultant (GCP led), you will play a key role in shaping and delivering the organisation's quality framework, with a primary focus on GCP but with exposure across broader GxP disciplines (GLP / GMP depending on pipeline and scope). Key responsibilities will include: Supporting the development and streamlining of GCP SOPs Providing QA oversight of CROs and clinical vendors Conducting and supporting GCP audits (internal/vendor/study-level) Driving inspection readiness (MHRA/FDA/EMA) Advising on phase appropriate QMS build without overengineeringThis is a high-impact role, working closely with senior leadership in a growing biotech environment. What you'll need to succeed Proven experience within GCP QA in biotech or pharma environments Strong background supporting early clinical / FIH studies Experience building or improving QMS frameworks and SOPs Hands-on experience with audits and vendor oversight Ability to work autonomously in a fast-paced, evolving environmentWhat you'll get in return Opportunity to support a biotech at a critical inflection point Exposure to end-to-end QMS build and FIH readiness Flexible, high-autonomy contract environment Competitive RateWhat you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now