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About the Role: I'm partnered with an innovative, fast-paced, global medical device company with a mission to save lives by making every donated organ count. A commercial-stage business committed to improving transplantation outcomes throughout the world, their first product has been used to support more than 5,000 transplant operations globally, and they are growing fast. They are now looking for a highly motivated and detail-oriented Quality Auditor to join their dynamic Quality team. In this pivotal role, you will lead and execute internal audits across their sites and conduct supplier audits to ensure products are safe and effective, verify full alignment with their Quality Management System, regulatory requirements, and industry best practices. This is a business that takes quality seriously because what they make genuinely matters — and they're looking for someone who understands that distinction. If you think beyond checklists, see audits as an opportunity to strengthen a business rather than just verify it, and want to work somewhere where the work has real meaning, this is worth a conversation. Key Responsibilities • Plan and conduct internal and supplier product and manufacturing audits in accordance with quality agreements and regulatory requirements including ISO 13485:2016, FDA 21 CFR Part 820, and EU MDR, • Identify areas for improvement within the QMS and supplier systems, and support the implementation and verification of corrective actions, • Develop and deliver audit reports, communicate findings to management, and monitor the effectiveness of corrective measures, • Support the development and implementation of action plans based on audit outcomes, • Support supplier qualification activities through audits for approval and periodic re-evaluation, ensuring adherence to quality agreement requirements and managing updates or revisions as necessary, • Partner with Procurement and Product Quality teams, providing audit data to support supplier qualification and re-evaluation processes, and collaborating to monitor supplier performance, • Foster strong working relationships with suppliers to drive continuous improvement and compliance, • Participate in and support external inspections and audits including BSI Notified Body and FDA, • Stay current with changes in applicable quality regulations and standards, providing training and guidance to internal teams as needed Skills & Experience • Audit Experience: Minimum 3 years in ISO 13485 QA-focused roles, including at least 1 year of hands-on practical auditing. Lead Auditor certification in ISO 13485, MDR or MDSAP desirable, • Interpersonal Skills: The ideal candidate is able to build rapport with auditees, anticipate reactions, and deal professionally with all situations. This role requires emotional intelligence and the ability to communicate the value of audits, making stakeholders feel at ease while encouraging open dialogue and genuine collaboration., • Critical Thinking & Continuous Improvement Mindset: We're looking for someone who thinks beyond checklists, someone who can look at processes end-to-end, ask the right questions, and spot practical ways to improve efficiency, compliance and overall performance, benefiting both quality and business outcomes., • Analytical Abilities: Strong attention to detail and demonstrable experience with process improvement, • Technical Proficiency: Proficient in Microsoft Office applications including Excel, PowerPoint, Visio and Word. Knowledge of MasterControl and Power BI is advantageous., • Organisational Skills: Organised, detail-oriented, and able to multitask and prioritise responsibilities in a fast-paced environment Qualifications • University or college degree, preferably in life sciences, quality, or regulatory affairs, or an equivalent combination of education and experience, • Minimum 3 years of experience in medical device quality system auditing or equivalent Location: Oxford-based, 3 days on-site with 2 days work from home per week. Ideally within a 50-mile / 1-hour commute of Oxford. Travel: 10–15% across Europe and the US for supplier audits

Job purpose Reporting to the Director, Quality Operations EU/RoW (Molecular Imaging Platform), the Senior Manager Quality Operations, EU/RoW will be responsible for managing the quality operations of Blue Earth Diagnostics’ EU/RoW based third-party Contract Manufacturing Organisation (CMO) network and oversight of the supply chain. This includes ensuring that medicinal products supplied by the company are manufactured, released and distributed in compliance with UK, EU and RoW applicable laws and regulations. The position requires operational oversight and cross-functional collaboration to maintain a robust and consistent supply of quality products in accordance with regulatory requirements. Main Responsibilities, Activities, Duties and Tasks • Serve as the primary quality point of contact for EU/ RoW -based Contract Manufacturing Organizations (CMOs), overseeing manufacturing performance, resolution of quality-related issues and managing quality relationships with CMOs., • Qualify new CMOs and perform periodic requalification according to Blue Earth Diagnostics (BED) procedures., • Maintain and manage the risk-based audit schedule., • Ensure appropriate documentation and maintenance of quality oversight records, including routine monitoring and follow-up actions., • Manage and oversee CMO investigation reports, including analytical Out of Specifications, to ensure technical accuracy, regulatory compliance, and effective root cause analysis., • Lead routine quality meetings with CMOs to manage performance, deviations, complaints, changes, improvements, and escalations., • Gather data and perform trending and analysis of CMO performance and quality to proactively identify risks and drive continuous performance improvement., • Conduct scheduled on-site CMO audits in accordance with the annual audit schedule and manage approved contract auditors as applicable., • Work in accordance with quality risk management principles., • Support the continuous enhancement of the Blue Earth Diagnostics Quality Management System (QMS), including SOP revisions, process optimization, and alignment with global standards., • Contribute to the development and presentation of Quality Assurance metrics and reports for Quality Management Review (QMR)., • Monitor regulatory changes related to EU PET and pharmaceutical manufacturing, quality, and distribution; evaluate impact and initiate updates to internal processes as needed., • Assess, document, and track complaints, deviations, and CAPAs to ensure timely, thorough, and effective resolution and preventive action., • Operate in compliance with the Blue Earth Diagnostics Quality Management System and regulatory requirements., • Train, coach and support Blue Earth Diagnostics personnel in quality and compliance requirements. Education A degree in a science related discipline is desirable. Professional Experience, Knowledge & Technical Skills • Comprehensive knowledge of EU GMP regulatory legislation and ICH guidelines obtained within sterile and/or radiopharmaceutical Manufacturing operations. Knowledge of US CFR is desirable., • Experience with hosting or acting as SME for Regulatory Authority GxP inspection process., • Trained GxP auditor or having sufficient knowledge and experience to perform GxP audits and to assess, select and manage/oversee contract GxP auditors and maintain the audit schedule., • Experience with Positron Emission Tomography (PET) or radiopharmaceutical products is strongly preferred., • Demonstrated experience overseeing and managing third-party Contract Manufacturing Organizations (CMOs) or other suppliers, including performance monitoring and issue resolution., • Comprehensive understanding of Quality Management System (QMS) principles, quality oversight, deviation management, CAPA, change control, and quality risk management practices., • Proven ability to collect, consolidate, analyze, and interpret operational and quality performance data to generate meaningful information, • Excellent investigation, problem solving, and report writing skills., • Excellent written and verbal communication skills, negotiation, collaboration, and interpersonal skills with ability to work effectively with others at all levels of the organization., • Ability to influence and build relationships/earn credibility quickly across broad global constituencies with competing priorities., • Highly skilled or advanced knowledge of Microsoft 365 package (i.e., Word, Excel, PowerPoint) and experience with Power BI is desired but not essential.

Our Client Mackie Myers have partnered with a fast-growing, private equity backed organisation in Oxford to appoint a Group Financial Accountant into their expanding Group Finance team. This role is a fantastic stepping stone for technical finance candidate to progress their career within a private equity organisation. The Role The Group Accountant will take ownership of the group consolidation process, statutory reporting, and financial oversight across multiple entities within the group. This role is central to delivering accurate, timely, and compliant financial information, while partnering with subsidiary finance teams and senior stakeholders to enhance reporting quality and insight. You will contribute to strengthening controls, improving systems integration, and supporting technical accounting matters across the group. This position provides strong exposure to senior leadership and the opportunity to influence process improvements within a developing finance function. Main Duties • Lead monthly and annual group consolidations, including sub-consolidations and consolidation journals, • Manage intercompany reconciliations and ensure timely resolution of reconciling items, • Prepare consolidated and entity-level financial statements in line with IFRS / UK GAAP, • Produce board reporting packs including financial analysis, commentary, and KPIs, • Oversee reporting timetables to ensure accurate and timely delivery of results, • Support statutory reporting requirements and coordinate the year-end audit process, • Prepare consolidation schedules and respond to auditor, tax advisor, and lender queries, • Maintain key balance sheet schedules, including fixed asset registers, • Ensure effective integration between ERP and consolidation systems, maintaining system mappings, • Drive continuous improvement across reporting processes, controls, and KPI development The Successful Candidate • Qualified accountant (ACA Preferred, ACCA & CIMA also considered), • Practice experience within a top 10 firm, • Strong technical accounting knowledge, • Excellent analytical skills with strong communication and stakeholder engagement abilities, • Proactive, detail-oriented, and motivated to grow within a fast-paced business, • PowerBI experience What’s on Offer? • £60,000-75,000 per annum, • Competitive benefits package, • Private equity experience, • Opportunity to work in a dynamic, fast-growing business with clear progression Our Commitment to Equality, Diversity, and Inclusion We believe that diverse teams drive innovation and success. That's why we're committed to promoting equality of opportunity and creating inclusive workplaces where everyone feels valued and supported. We actively seek out talent from all backgrounds and strive to reflect the rich diversity of the workforce in every role we recruit for.

Audit Senior Location: Oxford Contract: Full-time, Permanent Salary: Competitive, based on experience About the Firm A highly regarded accountancy firm with a strong presence in Oxford is seeking an experienced Audit Senior to join its expanding audit team. The firm is known for its high-quality, forward-thinking approach and its commitment to developing both clients and staff within a supportive and collaborative culture. The Role The Audit Senior will take responsibility for leading audit assignments from planning through to completion, working closely with managers and supervising junior team members. This position offers an excellent opportunity for an ambitious auditor who is looking to take the next step in their career within a progressive and growing practice. Key Responsibilities Leading audit engagements for a varied portfolio of clients across multiple sectors Managing audit planning, fieldwork, and completion processes Supervising and mentoring junior team members, providing feedback and on-the-job training Reviewing work completed by junior staff to ensure technical accuracy and quality Preparing draft financial statements and audit reports Building and maintaining strong client relationships, acting as a key point of contact during assignments Ensuring compliance w...

Supplier Quality Engineer - Medical Devices - Oxford A well‑funded and rapidly growing medical devices company in Oxford is seeking a Supplier Quality Engineer to support the management and development of its supplier base, ensuring that all goods entering and leaving the business meet the required standards. Newton Colmore is recruiting for this role exclusively, so applications must be made directly through us. In this position, you will be responsible for the continual evaluation of existing suppliers, the identification of new suppliers and the ongoing monitoring of supplier performance. You will ensure compliance with ISO 13485, manage CAPAs, apply your quality expertise to design‑for‑manufacture considerations and take on the broader responsibilities expected within a supplier quality function. Ideally, you will be a qualified Lead Auditor with experience working within an ISO 13485 environment. However, we are also open to candidates from other highly regulated sectors such as biotech or aerospace. The technology being manufactured is genuinely industry‑disrupting and has the potential to improve the lives of thousands of people worldwide. The company has secured significant funding due to the success of its device, providing long‑term stability and a strong platform for continued growth. In return, you will receive an excellent starting salary, private healthcare, income protection, life assu...

A pioneering medical technology firm in Oxford is seeking a Quality Auditor.

A global medical device company in Oxford is seeking a Quality Auditor to lead internal and supplier audits, ensuring compliance with quality standards. You will identify areas for improvement within the Quality Management System and foster strong relationships with suppliers. The ideal candidate ha

SocialCare #ChildrensServices #Ofsted #QualityAuditor #SocialCareJobs #Recruitment. I’m Recruiting – Quality Auditor | Children’s Services | £40K | Hybrid. Report writing and quality improvement recommendations.

Company description:Fantastic challenges.GKN Aerospace is reimagining air travel: going further, faster and greener! Fuelled by great people whose expertise and creativity sets the standards in our industry, were inspired by the opportunities to innovate and break boundaries.Were proud to play a par

Premier Recruitment Group is working in partnership with a well established and international organisation in Dartford to recruit a Quality Assurance Auditor to join their team.

Salary:Competitive salaryBenefits:Company share save scheme, Pension up to 8% matched, Life insurance up to 4x salaryLocation:Bourne, Lincolnshire, PE10 0ATWays of Working:Site basedHours of work:4 on 4 off / 6am 6pmContract Type:PermanentWhy Greencore?Following the combination with Bakkavor in Jan

A leading convenience food manufacturer in Greater Lincolnshire is seeking a Quality Auditor to enhance quality systems and food safety standards. The ideal candidate will have strong analytical and communication skills, ensuring high-quality standards are met on-site.

Reporting to the Head of Quality the Quality and Compliance auditor will take a central role in the regulatory compliance audit function within Consensus. The role is instrumental in driving quality outcomes for the people we support and is a key role in reaching our aspirations to be the best quali

A leading water company in the UK is seeking a Quality Scientist to join their Laboratory Quality Team. The role involves supporting the Quality Manager, conducting audits, and ensuring compliance with ISO17025 and quality standards.

A UK food business is seeking a Quality Auditor to ensure product quality and safety in a dynamic FMCG factory. Responsibilities include quality checks, data recording, and supporting the QA team.

A leading recruitment agency is seeking a Quality Controller to ensure product quality and compliance with safety and regulatory standards. This role involves implementing quality procedures, conducting audits, and managing inspections while driving continuous improvement in production processes. Id

A leading care provider in the UK is seeking a Quality & Compliance Auditor to ensure regulatory compliance and drive quality outcomes. The position involves planning audits, producing reports, and collaborating with operational teams to improve service quality.

Here at MJ Quinn, we currently have an exciting new opportunity for a Quality Auditor to join the business. Here at MJ Quinn, we currently have an exciting new opportunity for a Quality Auditor to join the business. Quality Auditor - Derby Region.

A global certification company is seeking an experienced auditor to conduct ISO9001 and IATF16949 audits in the United Kingdom. Additional auditor qualifications are preferred.

A company in the food industry is seeking a QA Technician to provide quality assurance support, ensuring all food products meet safety and legal standards. Responsibilities include monitoring product compliance and maintaining quality assurance systems.

We're excited to be growing our quality team and are on the lookout for an experienced Quality Auditor. Sign in to set job alerts for “Quality Auditor” roles. You’ll also collaborate with our Quality Business Partners, Branch Managers, and operational leaders to drive best practice and continu

A leading social care recruitment agency is seeking a Quality Auditor to provide independent assurance on service compliance across children's homes in the West Midlands. This hybrid role involves on-site assessments, compliance checks against regulations, and quality improvement recommendations.

A global automotive solutions provider is seeking a Spare Parts Process Quality Supplier Auditor in England. Responsibilities include managing quality processes for suppliers and ensuring compliance with OEM standards. Candidates should have a relevant engineering degree, strong analytical skills, a

A leading facilities management company in the UK is seeking a Compliance Officer to oversee clinical facilities and ensure adherence to health standards.This role involves conducting audits, managing compliance with safety regulations, and supporting continuous improvement initiatives.The ideal can

A global automotive solutions provider in the UK is looking for an individual to manage Aftersales spare parts quality and supplier coordination. The role encompasses supporting supplier production relocations and ensuring compliance with quality management processes.

Reporting to the Head of Quality the Quality and Compliance auditor will take a central role in the regulatory compliance audit function within Consensus. The role is instrumental in driving quality outcomes for the people we support and is a key role in reaching our aspirations to be the best quali

Assist the Quality Manager in the daily supervision and management of the Quality Assurance team. In this role you will assist in supervision and management of the Quality Assurance team, organise tasks and workload of the QA team, audit the production process against the latest legislation, agreed

A leading engineering firm is seeking a Supplier Quality Engineer near Bristol. This full-time hybrid role involves ensuring the delivery of high-quality components and materials from suppliers.

A financial services company in Greater London is seeking a Sales Quality professional to monitor sales competencies and due diligence.

This role focuses on maintaining high standards in audits related to quality and food safety.

The role is to provide Aftersales spare parts quality management process support for key aspects of the suppliers Quality Management Team. This service must be provided using sound automotive parts quality management methodology & practices and a working knowledge of Parts Quality management systems

A leading healthcare provider in Greater London is seeking a Clinical Auditor for its ADHD services to improve patient care through clinical audits and data analysis. The successful candidate will have clinical healthcare qualifications, at least five years of experience, and a commitment to enhanci

Quality Auditor - Childrens Services — Location Midlands / Yorkshire (Hybrid - 3 days onsite auditing).

Junior QA Assistant / Quality Assistant. We have an exciting opportunity for a Junior QA Assistant / Quality Assistant to join the Technical Department of a growing, award-winning, family-owned food manufacturer. Reporting to the Technical Manager, you will support all aspects of the Technical funct

Join a vibrant team dedicated to quality and safety.

Quality & Compliance Auditor - Children's Services. To deliver independent assurance on service-level compliance with statutory regulations and internal quality frameworks, identifying risks, areas of non-compliance, and opportunities for improvement. Experience of auditing, inspection, or quality a

A recruitment agency is seeking a Quality Auditor to join a team in East Lindsey. Apply now to be part of a dynamic team focused on quality assurance. The role involves implementing quality control measures for product lines, ensuring compliance with industry standards, and conducting various audits

A successful engineering company based in Gloucestershire is seeking a Quality Systems Auditor to ensure compliance with industry standards and drive continuous improvement.

In this busy and hands-on role as a Quality Auditor, you'll audit, monitor, and continuously improve quality systems and procedures across site operations. Working closely with operational teams, you'll provide practical technical support while maintaining and promoting quality and food safety stand

We have an exciting opportunity for a Junior QA Assistant / Quality Assistant to join the Technical Department of a growing, award-winning, family-owned food manufacturer. Reporting to the Technical Manager, you will support all aspects of the Technical function, playing an active role in developing

A leading care provider is seeking a Quality & Compliance Auditor to ensure 100% compliance across regulatory systems. Responsibilities include conducting audits, producing reports, and driving quality improvements while supporting individuals with learning disabilities and complex needs.

A growing food manufacturer is seeking a Junior QA Assistant to support the Technical Department in ensuring compliance with food safety and quality standards. The company fosters a supportive environment for career development in food quality.

Responsibilities include managing the Quality Department, driving quality culture, and ensuring compliance with regulations. A long established print firm in South Yorkshire is looking for a meticulous Quality Manager.