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As the Regional HSEQ Compliance Auditor, you will be responsible for undertaking & delivering the regional HSEQ compliance audit plans for the business. You will collectively be undertaking risk-based audits to ensure HSEQ standards are being adhered to and providing assurance that contractual requirements are being met. In addition, you will also support the Group Quality Manager during external HSEQ audits to maintain accreditations. This will involve auditing the onsite activities of the Network Plus Group, its subsidiaries businesses, the regional depots and in some cases will also include our sub-contractors activities. As part of this role, you will be responsible for managing a non-conformance database detailing findings from audits, including follow up and close out. You will be required to provide stakeholders with visibility of all non-conformances and improvement opportunities. You will have a passion for ensuring exceptional levels of health, safety, quality and environmental standards are delivered. You will possess an attention to detail to ensure that audit reports are completed to a professional standard and are presentable to all business stakeholders. (internal & external stakeholders) • Work with the Group Internal Audit Manager to develop implement and monitor an effective regional assurance program to cover risks detailed within the HSEQ Risk Register and ensure compliance with Network Plus’s safety standards and regulatory requirements., • Undertake HSEQ Compliance Audits in line with Group assurance programme, coordinate with auditees to ensure audits are undertaken on live worksites. (our worksites can be of a short duration and may involve occasional night visits to traffic management activities)., • Undertake HSEQ Compliance Audits in line with Group assurance programme, within our offices and depots, coordinate with auditees as to ensure audits are undertaken with relevant personnel present., • Support the Group Quality Manager in co-ordination of external audits, accreditation body and client audits., • Provide a consistent approach and identification non-conformances and opportunities for improvement and the escalate areas of potential impact., • Undertake audit close out meetings with auditees, support their understanding on findings, audit actions, closure plans and timescales., • Provide regular data and management reports in line with the governance structure on audit action management, and any learning from experience identified., • Collate and provide back to group audit closure evidence as required / requested., • You will support & drive the correct and safe behaviours out on site and within the offices & depots Essential • Recognised Lead Auditor Qualification, • Recognised Internal Auditor Qualification, • ISO 45001, 14001 and 9001 Awareness, • Working knowledge of SIPP and CDM, • Experience in a similar HSEQ Auditor role, • Working knowledge of ISO 45001, 14001 & 90001, • Working knowledge of CDM requirements, • Demonstrable Project Management Capability, • Proven experience of undertaking auditing activities within a utility /construction environment., • Full UK Driving Licence Desirable, • Utilities experience, • Knowledge of NHSS ( National Highways Sector Schemes), • Knowledge of NERs, WIRs & GIRs schemes ( Electricity, Water, Gas -Industry Regulatory schemes), • HSEQ Qualification e.g. NEBOSH Diploma (or equivalent), • Chartered Practitioner or working towards We offer a competitive salary based on experience along with a full benefits package. Network Plus is proud to be an Equal Opportunity Employer. We celebrate diversity and do not discriminate based on race, religion, colour, nationality, sex, sexual orientation, age, veteran status, disability status, or any other applicable characteristics protected by law. We are Armed Forces-friendly. We welcome applications from ex-Armed Forces personnel, reservists, armed forces veterans, cadet instructors and military spouses/partners. We understand that privacy and the security of your personal information is extremely important. By applying for this role, you agree to the terms of our privacy policy. Network Plus is an award-winning business delivering essential utility and infrastructure services for the UK’s major providers of gas, power, telecoms, transport, water, and wastewater. We value the variety of experience, perspective, and other points of difference our workforce, clients, and supply chain offer. We are actively working with colleagues across the Network Plus Group to develop an inclusive environment – we want all our employees to feel valued and included to enable everyone to thrive at work and understand the value of their contribution matters no matter their background, identity, or circumstances.

Description Programme: LCST (Logistics Commodities & Services Transformation) Location: Bristol Role Overview Leidos Europe Ltd is seeking a UK based Deputy Head of Compliance and Continuous Improvement who is a motivated self-starter who can work independently and as part of a team in a dynamic environment. You will be a dedicated resource to the Logistics Division working on the Ministry of Defence Logistics, Commodities and Services Transformation (LCST) Programme. Reporting to the Head of Compliance and Continuous Improvement, the Deputy Head will oversee a programme team quality function and the audit/assurance programme covering internal, external and supplier audits. You will be acting as the first point of contact for associated issues. As a key member of the compliance team, you will have tangible as well as strategic input within a growing business. You will be accountable for driving the culture of quality and compliance to the next level as the programme continues to expand. The role will be hybrid, with expectations to be in office at least twice a week and some travel will be required. Duties & Responsibilities: This position is a hands-on leader with strong background in quality assurance and quality control in an operational environment. The successful candidate will have strong analytical and problem-solving skills, a keen eye for detail, and evidence of CPD study on quality-related subjects. This position will work cross-functionally with our Defence customer, key sub-contractors and the operations teams to be ensure the quality programmes and procedures are of the highest standards so that we deliver products and services of the highest quality to our customers. Your responsibilities: • Overseeing programme wide quality processes to ensure compliance and risk mitigation, • Oversee development and self-inspections of the quality management systems, • A champion of continuous improvement you will support a culture of problem solving and service evolution, • The role will also drive forward on critical compliance topics such as ISO and AQAP activity, • Ensure that adequate records are maintained, • Ensure that all personnel are trained and aware of compliance and quality requirements, • Deputise for the Head of Compliance in both Customer and Key Sub-Contractor meetings, where necessary Skill Required: • Certification in a relevant discipline is necessary, as would working within an established quality team in an operations environment, • Holds ISO9001 Lead Auditor Qualification, • Experience implementing corrective and preventative actions (CAPA) and conducting Root Cause Analysis (RCA), • Proven experience working as an auditor alongside development, implementation and maintenance of quality systems is essential, • Credibility at a senior management level with the ability to influence senior stakeholders, • Experience of implementing continuous improvement methodologies (e.g. Lean, Six Sigma), • Experience of Internal, external and supplier auditing, • People management skills and the ability to develop others, • Willing to travel UK and Overseas Desirable Skills Required: • Experience working with MOD contracts, policies and procedures including AQAP, Defence Standards and Joint Service Publications., • Experience working with the following tools: Power BI, SharePoint, MS Office products (Word, Excel, PowerPoint), Jira, • Active SC security clearance Clearance Requirements: • BPSS Pre-screening required to start, • SC Required for role, • UK Citizenship Leidos UK! Join our team and discover a culture of collaboration, innovation, diversity, trust, caring management, communication transparency, work-life balance, and overall job satisfaction... What we do for you: At Leidos we are PASSIONATE about customer success, UNITED as a team and INSPIRED to make a difference. We offer meaningful and engaging careers, a collaborative culture, and support for your career goals, all while nurturing a healthy work-life balance. We provide an employment package that attracts, develops and retains only the best in talent. Our reward scheme includes: • Contributory Pension Scheme, • Private Medical Insurance, • 33 days Annual Leave (including public and privilege holidays), • Access to Flexible benefits (including life assurance, health schemes, gym memberships, annual buy and sell holidays and a cycle to work scheme), • Flexible Working Scheme Commitment to Diversity: We welcome applications from every part of the community and are committed to a truly diverse and inclusive culture. We foster a sense of belonging, welcoming all perspectives and contributions, and providing equal access to opportunities and resources for everyone. If you have a disability or need any reasonable adjustments during the application and selection stages please let us know, and we will respond in a way that best fits your needs. Who We Are: The ___ for the UK Ministry of Defence is a critical effort to enhance and improve the UK’s defence supply chain. The programme provides essential services such as storage and distribution for the MOD's materiel, including a global freight service and the procurement and inventory management of 70,000 commodity NATO Stock Number (NSNs). Working together as Team Leidos we are helping to transform the UK's defence supply chain by providing an integration of a complex mixture of services, at low risk, using a modern suite of systems that will deliver one version of the truth. For the first time, the MOD will see the whole picture, as it is happening. What Makes Us Different: Purpose: you can use your passion and abilities at Leidos to keep the people you care about safe. We are at the forefront of machine learning, AI, cyber security and solutions. Using your skills in the technology frontline by helping to build a safer world. You can inspire change. Collaboration: having flexibility to do your job is one of our core benefits, enabling you to become part of our extraordinary team. We have been empowering our people to work flexibly for years. Whether you work from home, the office or on customer sites, we will give you the digital tools and the flexibility to work smarter and align your needs and ours. People: Leidos empowers people from every background to be themselves and gives you the tools to learn new skills by enabling growth whilst developing. We believe that extraordinary people need opportunities to grow, to be inspired and to inspire others. At Leidos, we invest in technical academies, career rotations and a career development plans that enhance your future. If you're looking for comfort, keep scrolling. At Leidos, we outthink, outbuild, and outpace the status quo — because the mission demands it. We're not hiring followers. We're recruiting the ones who disrupt, provoke, and refuse to fail. Step 10 is ancient history. We're already at step 30 — and moving faster than anyone else dares. For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. £58,400.00-£74,900.00 The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law. About Leidos Leidos is an industry and technology leader serving government and commercial customers with smarter, more efficient digital and mission innovations. Headquartered in Reston, Virginia, with 47,000 global employees, Leidos reported annual revenues of approximately $16.7 billion for the fiscal year ended January 3, 2025. For more information, visit ___. Pay and Benefits Pay and benefits are fundamental to any career decision. That's why we craft compensation packages that reflect the importance of the work we do for our customers. Employment benefits include competitive compensation, Health and Wellness programs, Income Protection, Paid Leave and Retirement. More details are available at ___. Securing Your Data Beware of fake employment opportunities using Leidos’ name. Leidos will never ask you to provide payment-related information during any part of the employment application process (i.e., ask you for money), nor will Leidos ever advance money as part of the hiring process (i.e., send you a check or money order before doing any work). Further, Leidos will only communicate with you through emails that are generated by the Leidos.com automated system – never from free commercial services (e.g., Gmail, Yahoo, Hotmail) or via WhatsApp, Telegram, etc. If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at ___. If you believe you are the victim of a scam, contact your local law enforcement and report the incident to the ___. Commitment to Non-Discrimination All qualified applicants will receive consideration for employment without regard to sex, race, ethnicity, age, national origin, citizenship, religion, physical or mental disability, medical condition, genetic information, pregnancy, family structure, marital status, ancestry, domestic partner status, sexual orientation, gender identity or expression, veteran or military status, or any other basis prohibited by law. Leidos will also consider for employment qualified applicants with criminal histories consistent with relevant laws.

An Insurance firm are looking for an External Third-Party Auditor on a contracting basis for an initial 12-month period. The role will involve a third-party audit of their clients to make sure they are adhering to regulations, consumer duty and are handling claims correctly. There is already an internal framework in place to align to. The ideal candidate will have external audit experience and understand audit frameworks, ideally understand insurance or worked within an FCA regulated firm. Experience in Governance, Compliance, Complaints Handling, file reviewing, QA, claims is all useful.

Computer System Validation & GxP Compliance Consultant/Senior Consultant Pharmaceutical/Biotech — Remote (UK) - Multiple Positions Consultant and Senior Consultant Roles available - with an emphasis on Pharmacovigilance and Clinical knowledge Package: Excellent Hourly Rates (£75-£100 p/hr) offered in-line with Experience with potential of Salaried position. The Role in 20 Seconds You've spent a decade or more in pharmaceutical IT quality, validation, or GxP compliance. You've probably held titles like Validation Manager, QA Lead, CSV Lead, or IT Quality Manager — in a pharma sponsor, a biotech, a CRO, or a specialist consultancy. You know how to walk into a mid-size biotech on a Monday morning, pick up a statement of work, and get on with it. You're clinical or PV background means you can talk their language straight away. Our client is a specialist GxP and CSV consultancy that runs entirely on senior people. No juniors. No box-ticking. Their clients want experience and guidance. If that sounds like the kind of place you'd actually want to work, keep reading. The Company A lean, specialist consultancy delivering GxP compliance and CSV services to a client base predominantly in the USA, EU and UK. Their clients range from pre-revenue biotechs building their first quality management system to more mature pharma companies requiring specialist expertise for regulatory remediation, system validation, and audit programmes. They are mostly small to mid-sized clients with exciting product portfolios, generally in the "30–200 employee" range. These are organisations sophisticated enough to know exactly what they need, but lean enough that they don't have the internal QA resource to do it themselves. That's the gap this consultancy fills, and it's why the work is genuinely interesting rather than purely procedural. The model is deliberately small. Only experienced consultants are deployed. The quality of the work product is the commercial proposition, which means the people doing it have to be good. There's no layer of management between you and the client, and no junior to pass the awkward bits to. Some people find that energising. Those are the people we're looking for. The team is small, friendly, and above all, hardworking. They all share the same work ethic, and they are enjoying rapid growth - hence the reason for hiring. What You'll Actually Do The bread and butter: • Lead validation projects end-to-end — or execute defined work packages within them, depending on where you sit, • Plan and conduct GxP vendor audits of technology providers, from agenda to audit report to corrective action closure, • Author and renovate SOP suites, data integrity policies, change control frameworks, and vendor qualification programmes, • Deliver gap analyses and inspection readiness support that actually prepares people, rather than producing a report that sits in a drawer, • Act as the primary client contact on engagements — chairing meetings, managing stakeholder relationships, and presenting findings to senior quality and IT leadership The less obvious bits that matter as much: • Having the confidence to push back on a client when something is wrong — and the judgment to know when to pick that battle, • Translating complex regulatory requirements into proportionate, practical actions without gold-plating and without cutting corners, • Keeping an engagement on track and within budget whilst also managing the client expectations Who We're Looking For You'll be a natural fit if: • You've come up through pharmaceutical quality, validation, or IT compliance — in a sponsor, a biotech, a CRO, or a consultancy — and you've genuinely owned deliverables, not just contributed to them, • You're the person colleagues come to when there's a regulatory question that actually matters, rather than one that can be answered by reading the SOP, • You ask smart questions early rather than making assumptions, and your documentation doesn't come back needing heavy rework, • You're comfortable working independently in a remote model with real deadlines and defined accountability, • At the senior end — you've been the responsible professional when a regulator walked in, and you know exactly what that feels like, • This is NOT a role for manufacturing or LIMS specialists - this is focussed more on those with a PV / Clinical make-up Essential: • 10+ years in pharmaceutical quality, validation, or GxP compliance in a regulated environment, • Hands-on experience with computer system validation or quality assurance — in a pharma, biotech, or CRO setting specifically, • Proven ability to write inspection-ready documentation: validation plans, risk assessments, qualification protocols (IQ/OQ/PQ), and audit reports., • High degree of working familiarity with GAMP 5 concepts (software categories, V-model, risk-based testing) and key regulations such as ICH E6(R3), EU Annex 11, 21 CFR Part 11, and the FDA Computer Software Assurance (CSA) Guidance, February 2026., • Right to work in the UK without sponsorship Nice to have: • Previous experience in a client-facing consultancy role as opposed to purely in-house, • Inspection experience with FDA, MHRA, or EMA involving computerised systems, • Familiarity with eQMS implementation, data migration validation, or AI/ML in a GxP context, • RQA, ISPE, or DIA involvement, • ISO 27001 awareness or Lead Auditor certification. What's Actually In It For You The practical stuff: • Rates/salary based genuinely on experience — we won't be trying to lowball you at interview, • Remote working as the default — occasional client site visits, planned in advance, • Contract or permanent — both considered depending on what works for you, • Fractional engagements across multiple clients usually 1-2 month assignments The things that don't show up in a rate card: • Clients who are building something — clinical-stage biotechs constructing their quality infrastructure from scratch as they advance through trials, not large pharma running the same validation cycle they've run for twenty years, • Direct relationships with QA Directors, heads of IT, COOs, and occasionally CEOs — because with staff rosters of 30–200 people, that's who you're talking to, • A client list where your name is on the work, not buried four layers down in a consulting pyramid, • No internal politics to navigate — small team, clear accountabilities, • The satisfaction of handing over something that will genuinely hold up under inspection The Honest Bit This is not a nine-to-five with a clear desk at five. Client deadlines are real, inspection windows don't move, and occasionally a deliverable needs to be right by Friday regardless of when it landed in your inbox. Remote working in a fractional/contract model requires genuine self-management — there's no office to walk into and no one tracking your hours, so the only thing that matters is whether the work is good and the client is happy. If you've spent your career in large pharma with a lot of internal support around you, the step to a lean consultancy model can be bigger than it looks. If you've done it before, or if the idea of that autonomy is what's been missing from your current role, you'll probably love it. 📧 Apply via the link, or message Andy Clarke directly if you want to talk it through first — especially if you're weighing up the contract versus permanent question, or not sure whether your specific background is the right fit. 💼 Andy has been in and around regulated life sciences for over two decades. You'll get a straight answer to a straight question, not a sales pitch. All applications are treated confidentially. Guess what... We're not only interested in the conventional CV. Spent fifteen years in-house at a pharma and want to move to consultancy? Coming from a CRO and want to work across a broader client base? Built your validation knowledge in a regulatory technology company rather than a sponsor? Get in touch. If the experience is real and the documentation quality is there, the background matters less than you might think.

This is an exciting opportunity for a Senior Auditor with experience in the FMCG industry to join a thriving organisation in Bristol. The role involves conducting audits, ensuring compliance, and providing valuable insights to support financial decision-making. Client Details Our client is a well-established, large organisation in the FMCG industry, known for its innovative approach and commitment to excellence. Operating in a fast-paced and competitive environment, they are dedicated to maintaining high standards in their operations. Description • Plan, execute, and report on internal audits across various business functions., • Evaluate the effectiveness of internal controls and recommend improvements., • Ensure compliance with internal policies and external regulations., • Collaborate with stakeholders to address audit findings and implement corrective actions., • Prepare detailed audit reports for management and relevant stakeholders., • Monitor risk management processes and highlight potential risks to the organisation., • Provide insights to enhance operational efficiency and financial performance. A successful Senior Auditor should have: • Professional qualifications in accounting or auditing (e.g., ACA, ACCA, ...

Senior Internal Auditor - c.£44k annual bonus - Working from home/Bristol office As a Senior Internal Auditor you will be responsible for undertaking a range of complex and specialist audits at client's sites, in accordance with our Internal Audit standards. Working as an individual and leading a team to deliver high quality Internal Audits within required timescales and budgets. Brief Job description for a Senior Internal Auditor. • To understand the key risks identified by Management and the controls put in place to address those risks within each area of the Client’s Annual Audit Plan, • To manage, perform and control internal audit assignments embracing assignment planning programming, conduct and control of audit work and reporting findings, • To draft audit planning documents for approval / review by Client / Management, • Preparing draft audit reports and working paper files to high quality standards and within the SLA on allocated audits, adding value and good practice, • To lead and supervise more junior staff on individual assignments including staff motivation, discipline and technical audit guidance, • To provide job training and guidance for auditors and training for more junior auditors, • To perform the audit of more complex and specialist areas, • To undertake review work in respect of significant findings, • To assist management in ensu...

AssureBio is supporting a globally established pharmaceutical organisation in the appointment of a GVP QA Manager to strengthen its R&D Quality Assurance function. This is a high-impact role focused on pharmacovigilance quality oversight, vendor governance and regulatory inspection readiness within a global environment. You will operate as a key Quality Subject Matter Expert, ensuring robust compliance, patient safety and proactive regulatory readiness across pharmacovigilance and wider GxP activities. The position offers strong cross-functional exposure, working closely with senior stakeholders, global partners and regulatory bodies. Key Responsibilities GVP & R&D Quality Oversight • Provide leadership across pharmacovigilance QA activities within R&D and Scientific functions, • Act as SME for GVP/GxP compliance and provide expert regulatory interpretation, • Maintain oversight of Pharmacovigilance System Master File (PSMF) integrity, • Support quality due diligence for new product opportunities Audit & Vendor Management • Develop and maintain the R&D audit schedule, • Lead internal, vendor and third-party audits (acting as Lead or Co-Auditor), • Oversee quality performance of PV vendors and service providers, • Ensure effective audit closure and CAPA tracking Inspection Readiness & Compliance • Support regulatory inspection preparation and hosting (MHRA, EMA, FDA and global authorities), • Lead CAPA management arising from inspections and audits, • Provide risk-based QA advice to cross-functional teams, • Review and approve deviations, change controls and quality events Quality Systems & Continuous Improvement • Generate and present R&D quality metrics to senior stakeholders, • Deliver GxP training and guidance across the organisation, • Maintain awareness of evolving regulatory expectations and ensure business readiness, • Support continuous improvement of quality systems and processes This role is central to ensuring high standards of pharmacovigilance compliance, vendor oversight and inspection readiness across a complex global environment. Experience & Qualifications Essential • Scientific degree (Pharmacy, Chemistry, Biology, Engineering or related) or equivalent experience, • Significant QA experience within pharmaceutical and/or medical device environments, • Strong expertise in Good Pharmacovigilance Practice (GVP), • Proven experience supporting regulatory inspections and PV teams, • Experience in auditing, CAPA management and quality systems oversight, • Ability to operate autonomously and make risk-based quality decisions Desirable • Certification in auditing or Quality Systems Management, • Working knowledge of Good Clinical Practice (GCP), • Experience managing PV vendors and service providers, • Strong stakeholder engagement and influencing skills Candidates must demonstrate the ability to operate independently, provide strategic quality input and maintain strong regulatory compliance across global PV operations.

Financial Accountant Core3 are recruiting for a Financial Accountant to join our client on a fixed term contract basis in the North West of Bristol This is a hands-on opportunity within a complex business environment where you'll play a key role in delivering a high-quality month-end close and maintaining strong financial control. Why join our client Our client is a well-established, complex organisation with a collaborative finance team based in Bristol. They're focused on strengthening processes, improving consistency and building a finance function that adds real commercial value. You'll join during a period of positive change, with the opportunity to shape reporting and support better decision-making. As Financial Accountant in Bristol, you'll work in a hybrid pattern of 3 days in the office and 2 from home. How you'll make an impact Deliver an accurate and timely month-end close in line with reporting deadlines Prepare and review journals, ensuring compliance with internal controls Produce robust balance sheet reconciliations and resolve issues promptly Manage intercompany accounting and investigate reconciling differences Oversee fixed assets accounting and maintain the integrity of the asset register Support cash management and complete bank reconciliations Review transaction processing outputs and provide clear feedback Contribute to continuous improvement across financial control processes Respond to auditor and stakeholder queries with clarity and professionalism Why you're a great fit Qualified or part-qualified accountant (ACA, ACCA or CIMA) Strong experience in financial accounting within a complex business Proven delivery of month-end close, management accounts support and balance sheet control Confident using financial systems and advanced Excel Clear communicator, able to build relationships across finance and the wider business What you'll get in return As Financial Accountant, you'll enjoy real responsibility, supportive leadership and flexibility in Bristol. £45,000-£55,000 salary Hybrid working - 3 days in the Bristol office 9/12 month fixed term contract Pension and standard benefits package Opportunity to support process improvement initiatives| We welcome applications from all qualified candidates who believe they meet the role requirements. We're committed to equality, diversity and inclusion, and we'll provide any reasonable adjustments you may need throughout the recruitment process. If this advert sounds like you, please apply now or contact / Visit to view all our finance opportunities. TPBN1_UKTJ

Job Title: Quality Engineer Location: Bristol (Hybrid Working - On-Site 3 Days Per Week) Salary: £40,000 - £50,000 + Bonus & Benefits (Depending on Experience) Note: Only candidates with permanent, unrestricted UK working rights will be considered, as visa sponsorship is not offered for this position. Overview: Zenovo are supporting a repeat client, who are a growing engineering organisation in their search for a Quality Engineer with a strong mechanical and manufacturing background to join their team in Bristol. This role offers the opportunity to work closely with cross-functional teams including supply chain, goods-inwards, quality control, engineering, and sustaining. A successful candidate will take on a varied position, with responsibilities ranging from conducting supplier audits and developing supplier quality metrics, to auditing internal procedures and creating new processes to support ongoing business growth. This is an excellent opportunity for someone who enjoys a dynamic role and thrives in an environment where no two weeks are the same. Job Responsibilities: Investigate and resolve quality issues across internal teams, suppliers, and customers. Manage supplier issues/queries and ensure effective corrective actions. Support and improve the Quality Management System, including ISO9001 compliance. Collaborate with engineering, manufacturing, and supply chain teams to drive quality improvements. Assist with Quality and Inspection Plans and support Quality Control activities. Develop, review, and maintain procedures, process documentation, and quality plans. Conduct internal and external audits. Prepare and present quality reports to senior management, customers, and suppliers. Support KPI tracking and reporting. Experience Required: Minimum 3 years’ experience in a Quality Engineering role. Manufacturing/engineering background with the ability to read and interpret engineering drawings. Strong problem-solving skills with a proactive, detail-oriented, and results-driven approach. Experience with CMMs, inspection methods, and measurement equipment. Working knowledge of ISO9001 QMS, with familiarity of ISO14001, ISO45001, and ISO27001. Qualified ISO9001 auditor. Effective written and verbal communication skills. Proficient in Microsoft Office 365. Able to prioritise workload and meet objectives. Collaborative team player with strong cross-functional communication skills. Benefits Package Competitive pension scheme (up to 7% employer matched) Discretionary annual bonus (typically around 10%) 25 days annual leave plus 8 bank holidays Private medical healthcare Hybrid working and flexitime Annual wellness checks Retail vouchers Mental health support services If you’re interested in learning more about this opportunity, please apply with your latest CV

Abatec is assisting their client, a leading civil engineering and water contractor with the recruitment of a permanent Quality Manager to work out of their Welsh office of South West office. The successful candidate will take ownership of the organisation’s quality function, ensuring systems, processes, and standards are effectively implemented and consistently applied across the business. You will focus on maintaining compliance with regulatory and industry requirements, while identifying opportunities to improve performance and efficiency. This includes analysing quality data, addressing non-conformances, and driving practical improvements that add measurable value. Working closely with teams across the business, you will promote best practice, ensure clear communication of quality expectations, and support the delivery of reliable, high-standard outcomes. As Quality Manager you will: • Evaluate and enhance the existing Quality Management System (QMS) in line with industry best practice, • Lead the development and rollout of quality processes across the business, • Ensure compliance with ISO standards and applicable regulatory requirements, • Plan, conduct, and manage internal audits, while supporting external audit activities, • Work collaboratively with procurement and supply chain teams to uphold quality standards, • Manage non-conformance processes, including root cause analysis and corrective actions, • Oversee document control procedures and ensure accuracy of quality documentation, • Deliver training and guidance to teams on quality expectations and procedures, • Build strong relationships with stakeholders to ensure consistent quality outcomes Our client requires a Quality Manager with: • A minimum of 3 years’ experience in a Quality Management role in civil engineering or a similar field, • Proven track record of developing and managing Quality Management Systems, • Strong working knowledge of ISO standards (ISO 9001:2015 desirable), • Internal Auditor qualification (advantageous), • Excellent communication and stakeholder management skills, • Strong analytical mindset with effective problem-solving abilities Salary/Benefits: • £65,000 - £75,000 p/a, • Company vehicle / allowance, • 25 days holiday + bank holidays, • Pension Scheme, • Private healthcare, • Employee Assistance Programme If you would like more information, or to apply for this vacancy, please contact Lloyd Barham on (phone number removed). The reference for this vacancy is (phone number removed). We are always looking for candidates for similar positions, so please register your details with us to hear about similar opportunities that you may be interested in. Abatec Ltd. is working as an employment business on behalf of a client

Internal Auditor to join its in-house audit and risk function. This position will support the delivery of a business wide internal audit programme, covering a broad mix of operational and financial audits. We’re keen to speak with part-qualified or newly qualified auditors with at least one year o

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The role supports the achievement of business objectives by evaluating and reporting on the effectiveness of governance, risk management, and internal control processes in line with Internal Audit methodology and professional standards. You will collaborate with colleagues on internal audit engageme

Lutine Bell are excited to be partnering with a leading MGU and Specialty (Re)Insurance business as they look to appoint a Senior Internal Auditor to join their team in London. This individual will play a key role in executing the internal audit strategy within a dynamic and rapidly expanding organi

A reputable recruitment agency in London is seeking a Mandarin speaking Assistant Internal Auditor. The role involves assisting with internal audits, maintaining audit procedures, and preparing audit reports.

A global leader in investment banking and financial services, is seeking an experienced Internal Auditor to join the Compliance & Legal Internal Audit team, with a focus on Financial Crime & Compliance. In this role, you will conduct independent audits of the firm’s financial crime programs—spec

Your New Job Title: Mandarin speaking Assistant Internal Auditor / Internal Auditor. Assist the Head of Internal Audit in development of the Annual Internal Audit Plan for London Branch and submit to Senior Management/Head Office Internal Audit for approval. Candidates with experience in banking wou

A global healthcare firm is seeking a Senior Internal Auditor to evaluate controls within their dynamic audit team based in London.

The Internal Audit Assistant will support the Internal Audit team in executing the annual JSOX compliance process. Prepare and maintain documentation for internal controls and risk assessments. Internal Audit of IT processes and controls.

A leading international bank is seeking a Lead Internal Auditor to join its London-based internal audit team. You will also support audit planning and communication with senior management and group internal audit. The ideal candidate will have internal audit experience within banking or financial se

A financial technology firm in the UK is seeking a highly analytical Internal Auditor to enhance the effectiveness of internal controls and compliance frameworks.

A multinational engineering corporation is seeking a SOX specialist to join their internal audit team in the EMEA region. The role involves conducting SOX audits, evaluating internal controls, and analyzing complex data to enhance the SOX control environment.

A prominent financial services organisation located in the West Midlands is looking for a Senior Internal Auditor to perform risk-based audit reviews and engage with senior stakeholders. Additional benefits include a comprehensive holiday allowance, private medical insurance, and strong pension cont

Senior Internal Auditor or middle management Internal Audit role with exposure to a mixed portfolio of clients. Knowledge of Public Sector Internal Audit Standards and the mandatory elements of The Institute of Internal Auditors' International Professional Practices Framework (IPPF). Senior Auditor

A recruitment agency is seeking a newly or part qualified auditor to join a luxury hotel group in central London. This role involves planning and conducting various audits, evaluating internal controls, and collaborating with hotel teams to enhance processes.

We now require an additional, talented and enthusiastic Senior Internal Auditor to make a significant contribution to the work of our high-quality Internal Audit Section. Nottinghamshire County Council has an ongoing need for highly skilled, professional internal auditors to complete a range of chal

As a Senior Internal Auditor at NEXT plc, you will hold a pivotal position in providing independent, objective assurance and advisory services that underpin the Group’s continued success. Working closely with the Internal Audit Manager, you will play a lead role in delivering our risk-based audit

An opportunity has arisen for an Internal Auditor to join our Internal Audit function, with a particular focus on Compliance (Anti-Money Laundering and Financial Crime) and Corporate Governance. The Internal Auditor will be responsible for testing compliance with on policies and regulatory requireme

This is a critical hire at a pivotal time, as the business embarks on a significant strategic and digital transformation journey.We are seeking an experienced audit leader who can partner with executive leadership and provide robust oversight during a period of complex change.Proven audit leadership

A leading global Financial Services firm seeks an experienced Internal Auditor to focus on Compliance and Corporate Governance. The successful candidate will conduct internal audits, assist with regulatory compliance, and monitor effectiveness of policies.

Have a strong network within the internal audit community. BP and IT controls, working with our network of SOX auditors. A senior auditor with 4-6 years of BP SOX audit experience, both on the public accounting side, and in the industry (preferably for tech companies).

A global asset management firm in the United Kingdom is seeking an Auditor to support the Internal Audit Department.

A leading insurance firm is seeking an Internal Auditor to enhance the audit function. Candidates should have experience in internal audit within the insurance sector and strong analytical skills.