Cranleigh STEM is partnering with BioChek to appoint an Interim Quality Assurance Consultant to support the business through a critical transition period and site relocation project. This contract assignment requires an experienced QA professional to provide specialist quality and compliance expertise on a defined project basis. The successful consultant will take ownership of reviewing, improving and embedding key quality systems and processes, ensuring the organisation maintains compliance and operational effectiveness throughout a period of change.
Working closely with senior leadership and cross-functional teams, you will lead quality-focused project activities relating to QMS enhancement, compliance readiness and operational improvement.
You will act as a subject matter expert across quality assurance and compliance, supporting the business in strengthening systems, driving continuous improvement and maintaining ISO and GMP standards during a key growth phase.
Review, enhance and maintain the existing Quality Management System (QMS) Lead quality and compliance activities associated with the site transition project Review and improve document control processes, record management and archiving systems Identify and implement continuous improvement opportunities across QA processes Provide QA guidance and support to cross-functional stakeholders Produce and present quality metrics, reports and compliance updates to leadership teams Support customer complaint investigations and resolution activities Deliver training and coaching relating to quality systems and compliance best practice
Proven track record delivering QA projects within regulated environments Strong working knowledge of ISO9001 and GMP quality systems Previous experience supporting business change, transition or improvement projects Ability to work independently and provide expert QA guidance Strong stakeholder management and communication skills Proficient in Microsoft Office applications”, “datePosted”: “2026-05-23”, “hiringOrganization”: { “@type”: “Organization”, “name”: “BioChek – Smart Veterinary Diagnostics”, “sameAs”: “https://uk.whatjobs.com/pub_api__cpl__439453437__4861?utm_campaign=publisher&utm_medium=api&utm_source=4861” }, “jobLocation”: { “@type”: “Place”, “address”: { “@type”: “PostalAddress”, “addressLocality”: “” } } }
Interim Quality Assurance Consultant/Manager – BioChek Location : Contract: 3–6 Months / Outside IR35 Day/hourly Rate : Competitive
Cranleigh STEM is partnering with BioChek to appoint an Interim Quality Assurance Consultant to support the business through a critical transition period and site relocation project. This contract assignment requires an experienced QA professional to provide specialist quality and compliance expertise on a defined project basis. The successful consultant will take ownership of reviewing, improving and embedding key quality systems and processes, ensuring the organisation maintains compliance and operational effectiveness throughout a period of change.
Working closely with senior leadership and cross-functional teams, you will lead quality-focused project activities relating to QMS enhancement, compliance readiness and operational improvement.
You will act as a subject matter expert across quality assurance and compliance, supporting the business in strengthening systems, driving continuous improvement and maintaining ISO and GMP standards during a key growth phase.
Review, enhance and maintain the existing Quality Management System (QMS) Lead quality and compliance activities associated with the site transition project Review and improve document control processes, record management and archiving systems Identify and implement continuous improvement opportunities across QA processes Provide QA guidance and support to cross-functional stakeholders Produce and present quality metrics, reports and compliance updates to leadership teams Support customer complaint investigations and resolution activities Deliver training and coaching relating to quality systems and compliance best practice
Proven track record delivering QA projects within regulated environments Strong working knowledge of ISO9001 and GMP quality systems Previous experience supporting business change, transition or improvement projects Ability to work independently and provide expert QA guidance Strong stakeholder management and communication skills Proficient in Microsoft Office applications…