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Information Technology Auditor
Found in: Ziprecruiter UK C2 - 1 day ago
Locke and McCloud London, United KingdomJob Description · Information Technology Auditor | UK Hybrid | £40,000-£55,000 · Locke & McCloud are working with one of the top 10 Consultancy firms within the UK, they are looking for an Information Technology Auditor to come in and support their clients with ISO27001 and SOC 2 ...
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Information Technology Auditor
Found in: Appcast UK C C2 - 1 day ago
Locke and McCloud London, United KingdomInformation Technology Auditor | UK Hybrid | £40,000-£55,000 · Locke & McCloud are working with one of the top 10 Consultancy firms within the UK, they are looking for an Information Technology Auditor to come in and support their clients with ISO27001 and SOC 2 audits · This com ...
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Information Technology Auditor
Found in: Jooble UK O C2 - 2 days ago
Locke and McCloud London, United KingdomInformation Technology Auditor | UK Hybrid | £40,000-£55,000 · Locke & McCloud are working with one of the top 10 Consultancy firms within the UK, they are looking for an Information Technology Auditor to come in and support their clients with ISO27001 and SOC 2 audits · Speakin ...
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Senior Auditor, Technology
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Blueface Ltd United KingdomSenior Auditor, Technology page is loaded · Senior Auditor, Technology · Apply locations Great Britain - Isleworth, Sky 1 time type Full time posted on Posted Yesterday job requisition id R385466 Comcast brings together the best in media and technology. We drive innovation to c ...
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Information Technology Auditor
Found in: Jooble UK O L C2 - 1 day ago
Locke and McCloud London, United KingdomInformation Technology Auditor | UK Hybrid | £40,000-£55,000Locke & McCloud are working with one of the top 10 Consultancy firms within the UK, they are looking for an Information Technology Auditor to come in and support their clients with ISO27001 and SOC 2 auditsThis company a ...
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Information Technology Auditor
Found in: Jooble UK O L C2 - 1 day ago
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Auditor - Technology (Contract)
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Senior Auditor, Technology
Found in: Talent UK C2 - 2 days ago
Comcast Corporation Isleworth, United Kingdom Full timeComcast brings together the best in media and technology. We drive innovation to create the world's best entertainment and online experiences. As a Fortune 50 leader, we set the pace in a variety of innovative and fascinating businesses and create career opportunities across a wi ...
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Senior Auditor, Technology
Found in: Talent UK C2 - 2 days ago
Comcast Isleworth, United Kingdom Full timeDescription · Senior Auditor, Technology – Comcast Global Audit Team · Responsible for performing quarterly audit engagements year-round to help identify and manage risks to the business. Primary Responsibilities: · Participate as active members of the engagement team througho ...
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IT Auditor
Found in: SonicJobs Direct Apply UK - 16 hours ago
DGH Recruitment London, United Kingdom Full timeIT Auditor · Working as part of an IT Assurance team, you will be at the forefront of evolving audit standards, supporting financial audits, and navigating regulatory frameworks. You'll play a pivotal role in assessing and enhancing IT systems, processes, and controls, leveragin ...
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Group Reporting Manager
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Lead Internal Auditor`
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Lead Internal Auditor
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Lead Internal Auditor
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Project Security Lead
Found in: SonicJobs Direct Apply UK - 1 day ago
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Information Technology Audit Manager
Found in: Ziprecruiter UK C2 - 3 days ago
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Auditor - Technology (Contract) - United Kingdom - ProPharma Group
Description
GVP Auditor, Compliance & Quality Assurance (EU/UK) page is loaded GVP Auditor, Compliance & Quality Assurance (EU/UK)Apply locations Leiden Harlow time type Full time posted on Posted 30+ Days Ago job requisition id JR 358 ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving pharmaceutical, biotechnology, and medical device companies.
Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research solutions, life science consulting, R&D technology, pharmacovigilance, and medical information services to help solve complex challenges in a dynamic regulatory environment.
With our mission to improve the health and safety of patients, we are focused on delivering the highest quality of services throughout the full product lifecycle.
This remote position will be responsible for planning and conducting GVP/GCP audits as applicable (vendor (LPPV, CRO), clinical GVP mock regulatory inspection, PV, internal process, and investigator site) on behalf of clients.
The position of GVP Auditor will also act as a Subject Matter Expert (SME) for clinical-related projects and will be responsible for developing and managing the clinical auditing program.
This position is responsible for independently managing clinical-related projects and providing consulting and contract services to clients as needed.This position is also responsible for assisting with designing, implementing, monitoring, and maintaining ProPharma Group's GVP auditing program, policies and strategies and ensuring company compliance to GVP regulations, internal procedures, and policies in cooperation with peers.
The GVP Auditor will be subject matter lead for clinical consulting and auditing projects within ProPharma Group.Execute audits based on experience and a comprehensive understanding of all federal regulatory requirements and ICH (International Council for Harmonization) guidance on Good Clinical Practice (GCP) and guidance on Good Pharmacovigilance Practices (GVP).
The GVP Auditor will be a critical team member who contributes to the implementation of a risk based GVP audit program and provides oversight / management of the GVP consulting program.
Keep pace with advances and technological changes in clinical support Services within the pharmaceutical / device / biotech industries and promote those that will increase the company's effectiveness and profits.
Provide support to clients and all functional units of ProPharma Group as clinical compliance issues such as deviations and non-conformances arise.
Provides consultation for the implementation of proper CAPA to resolve deviations and non-conformances.Also, is responsible for helping to ensure compliance of company operations to quality principles and participation in the development of quality systems through SOP writing and training.
The GVP Auditor is responsible for promoting GVP subject expertise through publications and presentations through professional networks.The GVP Auditor will provide ongoing support and expertise to all personnel, assisting them in establishing goals, objectives, policies, and procedures for all applicable subsets of this business unit within the company.
Help to ensure the consulting practices are in compliance with all applicable internal and external policies procedures, and industry best practices.
Generation of proposals for GVP auditing and clinical-related projects.Assist Operations in staffing client projects to enable the company to execute the strategic plan efficiently and effectively, and to meet revenue and profit goals based on personnel skills development and client needs.
Audit GVP projects for correct approach, consistency, and quality.Ability to organize and manage projects.
Quality orientation and high attention to detail.
The role will guarantee the continued success of the company by ensuring that all employees, contractors, and the company as a whole meet or exceed established quality and compliance guidelines.
Utilize expertise of quality systems, data integrity, software compliance and GVP requirements to conduct audits and provide Gap analyses and risk assessments for clients.
Ability to manage and mentor colleagues in company GVP and clinical compliance related activities.This position will supported remotely with expectation for traveling for on-site audits and expectation to conduct virtual/remote audits.
University degree in scientific discipline as a minimum.
Minimum 10 years of clinical compliance and GVP auditing experience in related industry.
Minimum 5 years managing a technology business or business unit or applicable related experience.
We are committed to diversity, equity, and inclusion. Please, no phone calls or emails to anyone regarding this posting.**
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