QA Auditor

hVIVO; Greater London; On-site; GBP 45,000 - 65,000; Full time

Job summary

hVIVO is recruiting an experienced Quality Assurance Auditor for a permanent role based in London (E14, Canary Wharf). The position is site-based approximately 3 days per week.

The role entails auditing hVIVO processes, systems, facilities, studies and suppliers to deliver the audit programme in line with GCP and regulatory standards. Responsibilities include planning and conducting audits, reporting findings, and following up corrective actions across laboratories, data management, and related

Qualifications

• Demonstrated experience in quality assurance auditing and quality system experience.
• Excellent knowledge of GCP and GCP for laboratories regulatory standards.
• GCP or GCP for laboratories experience in pharmaceutical or CRO or NHS/Academia.
• Proven knowledge of drug development processes.
• 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.
• Degree in Science or equivalent desirable.

Responsibilities

• Plan and conduct audits of processes, systems, facilities, studies and documents to verify compliance and determine effectiveness of quality systems.
• Lead audits of low to medium risk suppliers and subcontractors, including remote audits.
• Lead on-site audits of high risk suppliers and ensure corrective actions are followed up.
• Close out audit findings with appropriate actions and responses.
• Maintain up-to-date knowledge of current regulations, guidelines and SOPs.

Skills

Quality assurance auditing

GCP / GLP knowledge

Regulatory compliance

Communication skills

Attention to detail

Problem solving

Education

Degree in Science or equivalent

Job description

hVIVO is recruiting for an experienced Quality Assurance Auditor. This is a permanent position based in London (E14, Canary Wharf) and is site based approximately 3 days per 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.

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.

Qualifications

• Demonstrated experience in quality assurance auditing and quality system experience;
• Excellent knowledge of GCP and GCP for laboratories regulatory standards;
• GCP or GCP for laboratories experience in pharmaceutical or CRO or NHS/Academia;
• Proven knowledge of drug development processes;
• 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;
• Degree in Science or equivalent desirable.