Senior QA Auditor (GCP)

hVIVO Services Limited; Greater London; Vor Ort; GBP 60.000 - 85.000; Vollzeit

Zusammenfassung

hVIVO Services Limited is seeking a Senior Quality Assurance Auditor to join our Canary Wharf, London site. The role focuses on ensuring compliance with SOPs, regulations, and ICH GCP standards, and conducting audits across processes, facilities, documents, and suppliers.

As a senior QA Auditor, you will plan, perform, and report audits, manage corrective actions, and stay up to date with industry guidance. This position is based in London with 2–3 days on site.

Qualifikationen

• Demonstrated experience in auditing suppliers, vendors, clinical sites and laboratories.
• Excellent knowledge of GCP and GCP for laboratories regulatory standards.
• Working knowledge of GLP and GMP standards.
• Proven communication skills with the ability to communicate with all levels within hVIVO.
• A pragmatic and diplomatic approach to problem solving.
• Excellent attention to detail.
• GCP or GCP for laboratories experience in pharmaceutical or CRO.
• Quality assurance auditing and quality system experience.

Aufgaben

• Plan and conduct audits of processes, systems, facilities, studies and documents in line with the audit programme to verify compliance and effectiveness.
• Plan and conduct audits of suppliers (remote) to hVIVO and assess risk.
• Lead on-site audits of high-risk suppliers and follow up actions.
• Close out audits with appropriate corrective actions and follow-up.
• Maintain up-to-date knowledge of current regulations, guidelines and SOPs.

Kenntnisse

Auditing suppliers

GCP for labs

GLP knowledge

GCP for laboratories

Strong communication

Detail oriented

Jobbeschreibung

Overview

hVIVO would like to recruit Senior Quality Assurance Auditor. This is a permanent position based in Canary Wharf (E14), London and is site based 2 or 3 days a week.

The main purpose of the role is to ensure that hVIVO are in compliance with the relevant SOPs, regulations and internationally recognised guidelines (including Statutory Instrument 2004 No. 1031 and its amendments, ICH GCP and GCP for laboratories). It is also to Conduct audits of all systems, processes, facilities, documents and studies within hVIVO and of suppliers and subcontractors to hVIVO in order to deliver the audit programme as required by GCP.

hVIVO conducts human challenge studies offering services to both pharmaceutical and biotechnology companies using a range of different clinical trial methodologies across differing viral challenges. The end goal of our clinical trials is to potentially eradicate common illnesses like the common cold and flu completely – or at least make treatment of them as easy and effective as possible. Volunteers are central to the work that we do. Our studies focus on testing new treatments on real people, in a safe, controlled, clinical environment.

Main Responsibilities

• Plan and conduct assigned audits of hVIVO processes, systems, facilities, studies and documents including protocols, reports, and computer system validation documents in line with the annual audit programme and appropriate study audit plans to verify compliance and determine the effectiveness of the company’s quality systems and procedures with agreed timescales;
• Plan and conduct assigned audits of low to medium risk suppliers and subcontractors to hVIVO by conduct of remote audits;
• Plan, conduct and follow up of audits of high risk suppliers performed at the suppliers on site premises;
• Follow up and close out all assigned audits including agreement of appropriateness of corrective actions to audit findings with relevant hVIVO staff;
• Assess compliance with the hVIVO Quality Management System (QMS) and ensure appropriate actions are agreed and effectively followed up;
• Maintain an up-to-date knowledge of the current regulations, guidelines and hVIVO SOPs.

Internal Audits

• Plan for audit by review of previous audit reports and relevant legislation and guidance;
• Produce audit plan where relevant to detail scope of the audit;
• Conduct allocated process, system, facility, study, document and data audits by review of relevant documentation, observing relevant procedures and tours;
• Assess compliance of the process, system, facility, study or document and categorise audit findings appropriately;
• Conduct audit close out meetings to present findings to relevant hVIVO staff;
• Produce audit report detailing audit summary, scope and findings and present for peer review;
• Conduct peer reviews of colleague’s audit reports to ensure accuracy and appropriateness of findings and classification of findings;
• Follow up of audit response not received within assigned timeframe;
• Assess audit responses for appropriateness of corrective and preventive actions and advise auditee on appropriate responses until agreement is reached;
• Conduct QA review of SOPs and associated Master Forms as part of review and approval system within QuMas;
• Plan, conduct and follow up audits across all business areas within hVIVO and all audit types and document types (laboratories, clinical, data management, computer system validation)

Audits of Suppliers and Subcontractors

• Plan, conduct and follow up allocated remote (questionnaire and due diligence) audits;
• Compile relevant questions to assess compliance of service being provided;
• Assess information provided or sourced to provide decision on suitability of supplier or subcontractor to provide services to hVIVO and add to QA approved suppliers list;
• Plan, conduct and follow up onsite audits in line with the supplier audit plan;
• Act as Lead Auditor to plan, conduct and follow up on-site audits of suppliers and subcontractors in line with the supplier audit plan;
• Liaise with relevant hVIVO staff requesting use of the supplier or subcontractor to ascertain scope of the audit required;

Hosting external audits

• Assist with external Sponsor audits and regulatory inspections;
• Manage the back room for Sponsor and regulatory audits;
• Liaise with relevant hVIVO staff in order to provide documents requested as part of the audit/inspection;
• Assist with compiling responses to audit reports from Sponsors and regulatory authorities.
• Compliance with Industry and Company Procedures and Training
• Have a sound knowledge of Industry regulations, guidelines and standards;
• Have a sound knowledge of business operational procedures and company documents and procedures;
• Where required attend external training courses and feedback information to QA;
• Be a member of RQA and keep up to date with current industry practices, regulatory requirements and industry news;
• Train and assess competency of Trainee QA Auditors and QA Auditors.

Skills & Experiences

• Demonstrated experience in auditing suppliers, vendors, clinical sites and laboratories
• Excellent knowledge of GCP and GCP for laboratories regulatory standards
• Working knowledge of GLP and GMP standards
• Proven communication skills with the ability to communicate with all levels within hVIVO
• A pragmatic and diplomatic approach to problem solving
• Excellent attention to detail
• GCP or GCP for laboratories experience in pharmaceutical or CRO
• Quality assurance auditing and quality system experience