Supplier Quality Engineer Plymouth, Devon Permanent Full-Time (Monday-Friday) Up to £50,000 (dependent on experience) Butler Rose is proud to be recruiting on behalf of a highly respected, Plymouth-based global manufacturer operating at the forefront of industrial and IT infrastructure solutions. Our client partners with some of the world's most recognised technology organisations across software, hardware and cloud computing. With continued growth and investment, they are seeking a talented Supplier Quality Engineer to join their Supply Chain team. The Opportunity This is an exciting opportunity to play a key role in ensuring supplier performance, quality assurance, and continuous improvement across a diverse and dynamic supply base. Working closely with suppliers, commodity buyers and customers, you will help ensure products meet the highest quality standards while supporting supplier development and compliance activities. Key Responsibilities Supplier Quality & Development Approve and set up new parts using Production Part Approval Process (PPAP) Work with suppliers to resolve quality issues and implement appropriate controls (inspection plans, SPC, control plans) Review supplier corrective actions, including root cause analysis and preventative measures Support supplier development through site visits (primarily UK-based) Supplier Selection & Audits Support identification and approval of new suppliers alongside commodity buyers Conduct supplier audits (remote and on-site) and agree improvement plans Develop a detailed understanding of supplier manufacturing and supply chain processes Quality Assurance & Compliance Manage parts rejection processes where products fail to meet specification or functional requirements Ensure material compliance with legal and customer requirements, including Full Material Disclosures (FMD) Review and submit supplier material content data Customer Interface Investigate customer complaints relating to purchased parts Identify root causes, provide feedback, and implement corrective and preventative actions About You We welcome applications from candidates with diverse backgrounds. To succeed in this role, you will bring: Essential: Experience in quality management or quality assurance Strong analytical and problem-solving capability (e.g. 8D methodology) Ability to interpret engineering drawings Knowledge of dimensional measurement and inspection techniques (SPC, control plans) High attention to detail and data accuracy Experience with ERP/MRP systems Strong communication skills with suppliers and customers Understanding of cosmetic quality standards Desirable: BSc in Quality Management or Engineering Quality-related qualifications (Diploma, Professional Certificate, Level 4 QA) Auditor or Lead Auditor qualification Experience with Process FMEA Experience coaching suppliers in quality systems SAP ERP knowledge Material content analysis experience Experience conducting supplier audits Understanding of manufacturing processes such as sheet metal stamping and injection mould tooling What's in It for You? Opportunity to make a meaningful impact Scope for innovation and continuous improvement Clear career development opportunities Supportive, collaborative working environment Recognition and performance-based rewards Rewards Package Up to £50,000 salary (dependent on experience) Company-wide bonus linked to attendance, productivity and quality 33 days annual leave (including bank holidays) plus holiday purchase scheme Pension contributions matched up to 5% Life insurance (3x salary) Health care provision Access to Smart Spending platform Please note: This role is not eligible for visa sponsorship. Applicants must have existing right to work in the UK. Employment is subject to DBS and sanction list checks in line with safeguarding and compliance requirements. If you're an experienced quality professional looking to take the next step in your career with a forward-thinking Plymouth manufacturer, we'd love to hear from you. Butler Rose is committed to equality in the workplace and is an equal opportunity employer.Butler Rose Ltd is acting as an Employment Business in relation to this vacancy.
Mar 18, 2026
Full time
Supplier Quality Engineer Plymouth, Devon Permanent Full-Time (Monday-Friday) Up to £50,000 (dependent on experience) Butler Rose is proud to be recruiting on behalf of a highly respected, Plymouth-based global manufacturer operating at the forefront of industrial and IT infrastructure solutions. Our client partners with some of the world's most recognised technology organisations across software, hardware and cloud computing. With continued growth and investment, they are seeking a talented Supplier Quality Engineer to join their Supply Chain team. The Opportunity This is an exciting opportunity to play a key role in ensuring supplier performance, quality assurance, and continuous improvement across a diverse and dynamic supply base. Working closely with suppliers, commodity buyers and customers, you will help ensure products meet the highest quality standards while supporting supplier development and compliance activities. Key Responsibilities Supplier Quality & Development Approve and set up new parts using Production Part Approval Process (PPAP) Work with suppliers to resolve quality issues and implement appropriate controls (inspection plans, SPC, control plans) Review supplier corrective actions, including root cause analysis and preventative measures Support supplier development through site visits (primarily UK-based) Supplier Selection & Audits Support identification and approval of new suppliers alongside commodity buyers Conduct supplier audits (remote and on-site) and agree improvement plans Develop a detailed understanding of supplier manufacturing and supply chain processes Quality Assurance & Compliance Manage parts rejection processes where products fail to meet specification or functional requirements Ensure material compliance with legal and customer requirements, including Full Material Disclosures (FMD) Review and submit supplier material content data Customer Interface Investigate customer complaints relating to purchased parts Identify root causes, provide feedback, and implement corrective and preventative actions About You We welcome applications from candidates with diverse backgrounds. To succeed in this role, you will bring: Essential: Experience in quality management or quality assurance Strong analytical and problem-solving capability (e.g. 8D methodology) Ability to interpret engineering drawings Knowledge of dimensional measurement and inspection techniques (SPC, control plans) High attention to detail and data accuracy Experience with ERP/MRP systems Strong communication skills with suppliers and customers Understanding of cosmetic quality standards Desirable: BSc in Quality Management or Engineering Quality-related qualifications (Diploma, Professional Certificate, Level 4 QA) Auditor or Lead Auditor qualification Experience with Process FMEA Experience coaching suppliers in quality systems SAP ERP knowledge Material content analysis experience Experience conducting supplier audits Understanding of manufacturing processes such as sheet metal stamping and injection mould tooling What's in It for You? Opportunity to make a meaningful impact Scope for innovation and continuous improvement Clear career development opportunities Supportive, collaborative working environment Recognition and performance-based rewards Rewards Package Up to £50,000 salary (dependent on experience) Company-wide bonus linked to attendance, productivity and quality 33 days annual leave (including bank holidays) plus holiday purchase scheme Pension contributions matched up to 5% Life insurance (3x salary) Health care provision Access to Smart Spending platform Please note: This role is not eligible for visa sponsorship. Applicants must have existing right to work in the UK. Employment is subject to DBS and sanction list checks in line with safeguarding and compliance requirements. If you're an experienced quality professional looking to take the next step in your career with a forward-thinking Plymouth manufacturer, we'd love to hear from you. Butler Rose is committed to equality in the workplace and is an equal opportunity employer.Butler Rose Ltd is acting as an Employment Business in relation to this vacancy.
Premier Technical Recruitment Ltd
Tewkesbury, Gloucestershire
Quality Engineer Gloucestershire - commutable from Cheltenham, Tewkesbury and Gloucester To c£42k neg dep exp + generous benefits Our client has been established for almost half a century and specialise in the provision of precision engineered components and solutions for supply across a diverse range of industry sectors worldwide. They are now seeking to recruit an experienced and enthusiastic Quality Engineer to complement their professional quality team, and both develop and lead quality related improvement programmes and internal opportunities for improvement. Actively involved in the NPI process ensuring all Quality requirements are understood and implemented, including the generation of associated downstream QA documentation, you will also be heavily involved with both third-party supplier audits and internal audits to ensure that the HPE management system is delivering expected results. As a Quality Engineer, you will be responsible for ensuring that product quality requirements are not compromised through process changes, and will be actively involved and work closely with Operations / Shop Floor, Customers and Suppliers in order to ensure that non-conformances are investigated, remediated and effective corrective actions are implemented as a priority. Core responsibilities will include (but not be limited to): Creating QA documentation (FAIR, Quality Plans, Inspection Test Plans etc) Applying quality tools and techniques to effect robust non-conformance investigation and resolution (including MAS (R&R), SPC, RCA & CAPA, APQP, FAIR, PPAP ) Reading and interpreting technical Engineering Drawings (GD&T) Motivating and leading multi-disciplined teams across the entire business. To be considered for this varied and challenging Quality Engineer role based near Tewkesbury it is envisaged that the successful candidate will possess strong knowledge and experience of PPAP and RCA techniques with the ability to write problem definitions / statements clearly and succinctly. You will be skilled in implementing effective monitoring / metrics to support corrective actions and have demonstrable experience of working with First Article Inspections as per AS9102, with additional knowledge and experience of machining processes (CNC & conventional) proving distinctly advantageous. With considerable proven Quality Engineering experience gained within a production environment and realistically qualified to at least HNC level or above in a relevant Mechanical, Manufacturing or Production Engineering discipline, you will also have undertaken External Auditor Training and be qualified to Lean Six Sigma Green Belt level or above. Experience of CMM programming, organisation and planning will again prove advantageous, with the ability to maintain a high level of attention to detail within a precision engineering environment and be able to work both autonomously and as part of a team essential requirements for the position. Contact the Quality Team at Premier Technical Recruitment on or email your cv in confidence to for further details.
Mar 18, 2026
Full time
Quality Engineer Gloucestershire - commutable from Cheltenham, Tewkesbury and Gloucester To c£42k neg dep exp + generous benefits Our client has been established for almost half a century and specialise in the provision of precision engineered components and solutions for supply across a diverse range of industry sectors worldwide. They are now seeking to recruit an experienced and enthusiastic Quality Engineer to complement their professional quality team, and both develop and lead quality related improvement programmes and internal opportunities for improvement. Actively involved in the NPI process ensuring all Quality requirements are understood and implemented, including the generation of associated downstream QA documentation, you will also be heavily involved with both third-party supplier audits and internal audits to ensure that the HPE management system is delivering expected results. As a Quality Engineer, you will be responsible for ensuring that product quality requirements are not compromised through process changes, and will be actively involved and work closely with Operations / Shop Floor, Customers and Suppliers in order to ensure that non-conformances are investigated, remediated and effective corrective actions are implemented as a priority. Core responsibilities will include (but not be limited to): Creating QA documentation (FAIR, Quality Plans, Inspection Test Plans etc) Applying quality tools and techniques to effect robust non-conformance investigation and resolution (including MAS (R&R), SPC, RCA & CAPA, APQP, FAIR, PPAP ) Reading and interpreting technical Engineering Drawings (GD&T) Motivating and leading multi-disciplined teams across the entire business. To be considered for this varied and challenging Quality Engineer role based near Tewkesbury it is envisaged that the successful candidate will possess strong knowledge and experience of PPAP and RCA techniques with the ability to write problem definitions / statements clearly and succinctly. You will be skilled in implementing effective monitoring / metrics to support corrective actions and have demonstrable experience of working with First Article Inspections as per AS9102, with additional knowledge and experience of machining processes (CNC & conventional) proving distinctly advantageous. With considerable proven Quality Engineering experience gained within a production environment and realistically qualified to at least HNC level or above in a relevant Mechanical, Manufacturing or Production Engineering discipline, you will also have undertaken External Auditor Training and be qualified to Lean Six Sigma Green Belt level or above. Experience of CMM programming, organisation and planning will again prove advantageous, with the ability to maintain a high level of attention to detail within a precision engineering environment and be able to work both autonomously and as part of a team essential requirements for the position. Contact the Quality Team at Premier Technical Recruitment on or email your cv in confidence to for further details.
Manufacturing Administrator Location: Near Yeovil Perm role £ 26,000 - 30,000 DOE My client, a well-established and successful family-owned FMCG manufacturing business, is seeking to appoint a Manufacturing Administrator / Stock and Sales Administrator for their facility located on the outskirts of Yeovil, near Wincanton. Operating from contemporary premises, the appointed Administrator will play a pivotal role within the office team, providing technical and quality support, managing stock administration for production, and assisting the accounts department with sales administration. This position is particularly suited to candidates possessing prior experience in manufacturing administration who are keen to further develop their careers. Key Responsibilities: Complete, process, and file documentation related to Goods In, Goods Out, and stock control. Support comprehensive stock traceability throughout the manufacturing process. Maintain accurate records using an ERP/MRP system. Assist with client sales, technical, and quality enquiries. Manage internal stock and facilitate physical stock checks. Provide general sales and office administrative support. Skills & Experience Required: Proficient in computer usage, preferably with experience in modern MRP systems, specifically Bills of Material. Previous background in manufacturing, food, beverage, pharmaceutical, or packaging industries is preferred. Strong analytical, numerical, and communication abilities. Exceptional attention to detail. Effective communication skills for regular interaction with factory personnel and customers. Excellent organisational skills, both written and verbal, essential due to the high volume of products managed. Collaborative team player, adept at multitasking and willing to be hands-on. Benefits: Competitive base salary (dependent on experience) 28 days holiday including bank holidays Pension scheme Modern kitchen facilities On-site parking Career development opportunities Open-plan office environment Christmas shutdown Working hours: Monday to Friday, 08:30-16:30 This role is commutable from Yeovil, Wincanton, Shepton mallet, Castle Cary, Martock, Somerton and may suit a candidate that has previously worked in stock control as a junior administrator, stock controller, QA Quality auditor, Technical administrator, ERP administrator, Technical assistant
Mar 17, 2026
Full time
Manufacturing Administrator Location: Near Yeovil Perm role £ 26,000 - 30,000 DOE My client, a well-established and successful family-owned FMCG manufacturing business, is seeking to appoint a Manufacturing Administrator / Stock and Sales Administrator for their facility located on the outskirts of Yeovil, near Wincanton. Operating from contemporary premises, the appointed Administrator will play a pivotal role within the office team, providing technical and quality support, managing stock administration for production, and assisting the accounts department with sales administration. This position is particularly suited to candidates possessing prior experience in manufacturing administration who are keen to further develop their careers. Key Responsibilities: Complete, process, and file documentation related to Goods In, Goods Out, and stock control. Support comprehensive stock traceability throughout the manufacturing process. Maintain accurate records using an ERP/MRP system. Assist with client sales, technical, and quality enquiries. Manage internal stock and facilitate physical stock checks. Provide general sales and office administrative support. Skills & Experience Required: Proficient in computer usage, preferably with experience in modern MRP systems, specifically Bills of Material. Previous background in manufacturing, food, beverage, pharmaceutical, or packaging industries is preferred. Strong analytical, numerical, and communication abilities. Exceptional attention to detail. Effective communication skills for regular interaction with factory personnel and customers. Excellent organisational skills, both written and verbal, essential due to the high volume of products managed. Collaborative team player, adept at multitasking and willing to be hands-on. Benefits: Competitive base salary (dependent on experience) 28 days holiday including bank holidays Pension scheme Modern kitchen facilities On-site parking Career development opportunities Open-plan office environment Christmas shutdown Working hours: Monday to Friday, 08:30-16:30 This role is commutable from Yeovil, Wincanton, Shepton mallet, Castle Cary, Martock, Somerton and may suit a candidate that has previously worked in stock control as a junior administrator, stock controller, QA Quality auditor, Technical administrator, ERP administrator, Technical assistant
Quality Assurance (QA) Manager Medical Device manufacturer. Based Northern UK - M62 / M1 circa Manchester, Leeds, Sheffield, Doncaster Base salary £60-70k (Negotiable) with Bonus and Package. Role Overview Our client is a global medical device manufacturer seeking an experienced and hands-on Quality Assurance Manager to lead their Quality function in a regulated manufacturing environment. This role is ideal for a Quality professional from the medical device, pharmaceutical, or chemical manufacturing sectors who can operate strategically and practically - including close collaboration with laboratory teams to support QA testing and compliance. The QA Manager will ensure regulatory compliance, maintain a robust Quality Management System (QMS), and drive a culture of quality, safety, and continuous improvement across the business. Office access required 2-3 days a week. Key Responsibilities Quality Management & Compliance Lead, maintain, and continuously improve the QMS in line with: ISO 9001 ISO 14001 GMP standards (applicable to the sector) UK MDR (for medical device components, if applicable) Ensure audit readiness at all times and maintain accurate quality records. Manage document control, change control, and staff training compliance systems. Lead Management Review and report on key quality metrics and KPIs. One direct head reports into the QA Manager. Laboratory & Product Quality Oversight Work closely with laboratory teams to oversee QA testing processes. Ensure handling, testing, and documentation of products meet regulatory and safety standards. Integrate quality systems within lab operations to maintain data integrity, traceability, and compliance. Support method validation, stability studies, and product testing as required. GMP & Audit Leadership Lead internal and supplier audits, ensuring effective follow-up and closure of CAPAs. Prepare for and support external audits from certification bodies, MHRA, or other regulatory authorities. Implement and oversee GMP standards across production and laboratory operations. HACCP & Environmental Compliance Maintain and develop HACCP systems where relevant. Ensure environmental compliance aligned with ISO 14001 standards. Monitor and drive improvements in environmental, safety, and quality performance. Key Requirements Proven experience as a Quality Manager in medical device, pharmaceutical, or chemical manufacturing. Strong understanding of laboratory QA testing and ability to integrate with lab teams. Practical experience with: ISO 9001 ISO 14001 HACCP GMP standards Experience leading and managing internal and external audits. Strong knowledge of risk management, CAPA processes, and regulatory compliance. Excellent organisational, leadership, and communication skills. Personal Attributes Detail-oriented, proactive, and solutions-focused. Comfortable working strategically and hands-on. Confident engaging with auditors, regulators, and cross-functional teams. Committed to fostering a culture of compliance, accountability, and continuous improvement. Why Join? Leadership role with visible impact on quality, compliance, and operational excellence. Opportunity to work across multiple regulated sectors - medical device, pharmaceutical, and chemical manufacturing. Collaborative culture with close integration between lab, production, and operations. Competitive salary and benefits package.
Mar 16, 2026
Full time
Quality Assurance (QA) Manager Medical Device manufacturer. Based Northern UK - M62 / M1 circa Manchester, Leeds, Sheffield, Doncaster Base salary £60-70k (Negotiable) with Bonus and Package. Role Overview Our client is a global medical device manufacturer seeking an experienced and hands-on Quality Assurance Manager to lead their Quality function in a regulated manufacturing environment. This role is ideal for a Quality professional from the medical device, pharmaceutical, or chemical manufacturing sectors who can operate strategically and practically - including close collaboration with laboratory teams to support QA testing and compliance. The QA Manager will ensure regulatory compliance, maintain a robust Quality Management System (QMS), and drive a culture of quality, safety, and continuous improvement across the business. Office access required 2-3 days a week. Key Responsibilities Quality Management & Compliance Lead, maintain, and continuously improve the QMS in line with: ISO 9001 ISO 14001 GMP standards (applicable to the sector) UK MDR (for medical device components, if applicable) Ensure audit readiness at all times and maintain accurate quality records. Manage document control, change control, and staff training compliance systems. Lead Management Review and report on key quality metrics and KPIs. One direct head reports into the QA Manager. Laboratory & Product Quality Oversight Work closely with laboratory teams to oversee QA testing processes. Ensure handling, testing, and documentation of products meet regulatory and safety standards. Integrate quality systems within lab operations to maintain data integrity, traceability, and compliance. Support method validation, stability studies, and product testing as required. GMP & Audit Leadership Lead internal and supplier audits, ensuring effective follow-up and closure of CAPAs. Prepare for and support external audits from certification bodies, MHRA, or other regulatory authorities. Implement and oversee GMP standards across production and laboratory operations. HACCP & Environmental Compliance Maintain and develop HACCP systems where relevant. Ensure environmental compliance aligned with ISO 14001 standards. Monitor and drive improvements in environmental, safety, and quality performance. Key Requirements Proven experience as a Quality Manager in medical device, pharmaceutical, or chemical manufacturing. Strong understanding of laboratory QA testing and ability to integrate with lab teams. Practical experience with: ISO 9001 ISO 14001 HACCP GMP standards Experience leading and managing internal and external audits. Strong knowledge of risk management, CAPA processes, and regulatory compliance. Excellent organisational, leadership, and communication skills. Personal Attributes Detail-oriented, proactive, and solutions-focused. Comfortable working strategically and hands-on. Confident engaging with auditors, regulators, and cross-functional teams. Committed to fostering a culture of compliance, accountability, and continuous improvement. Why Join? Leadership role with visible impact on quality, compliance, and operational excellence. Opportunity to work across multiple regulated sectors - medical device, pharmaceutical, and chemical manufacturing. Collaborative culture with close integration between lab, production, and operations. Competitive salary and benefits package.
Quality Assurance (QA) Manager Medical Device manufacturer. Based Northern UK - M62 / M1 circa Manchester, Leeds, Sheffield, Doncaster Base salary £60-70k (Negotiable) with Bonus and Package. Role Overview Our client is a global medical device manufacturer seeking an experienced and hands-on Quality Assurance Manager to lead their Quality function in a regulated manufacturing environment. This role is ideal for a Quality professional from the medical device, pharmaceutical, or chemical manufacturing sectors who can operate strategically and practically - including close collaboration with laboratory teams to support QA testing and compliance. The QA Manager will ensure regulatory compliance, maintain a robust Quality Management System (QMS), and drive a culture of quality, safety, and continuous improvement across the business. Office access required 2-3 days a week. Key Responsibilities Quality Management & Compliance Lead, maintain, and continuously improve the QMS in line with: ISO 9001 ISO 14001 GMP standards (applicable to the sector) UK MDR (for medical device components, if applicable) Ensure audit readiness at all times and maintain accurate quality records. Manage document control, change control, and staff training compliance systems. Lead Management Review and report on key quality metrics and KPIs. One direct head reports into the QA Manager. Laboratory & Product Quality Oversight Work closely with laboratory teams to oversee QA testing processes. Ensure handling, testing, and documentation of products meet regulatory and safety standards. Integrate quality systems within lab operations to maintain data integrity, traceability, and compliance. Support method validation, stability studies, and product testing as required. GMP & Audit Leadership Lead internal and supplier audits, ensuring effective follow-up and closure of CAPAs. Prepare for and support external audits from certification bodies, MHRA, or other regulatory authorities. Implement and oversee GMP standards across production and laboratory operations. HACCP & Environmental Compliance Maintain and develop HACCP systems where relevant. Ensure environmental compliance aligned with ISO 14001 standards. Monitor and drive improvements in environmental, safety, and quality performance. Key Requirements Proven experience as a Quality Manager in medical device, pharmaceutical, or chemical manufacturing. Strong understanding of laboratory QA testing and ability to integrate with lab teams. Practical experience with: ISO 9001 ISO 14001 HACCP GMP standards Experience leading and managing internal and external audits. Strong knowledge of risk management, CAPA processes, and regulatory compliance. Excellent organisational, leadership, and communication skills. Personal Attributes Detail-oriented, proactive, and solutions-focused. Comfortable working strategically and hands-on. Confident engaging with auditors, regulators, and cross-functional teams. Committed to fostering a culture of compliance, accountability, and continuous improvement. Why Join? Leadership role with visible impact on quality, compliance, and operational excellence. Opportunity to work across multiple regulated sectors - medical device, pharmaceutical, and chemical manufacturing. Collaborative culture with close integration between lab, production, and operations. Competitive salary and benefits package.
Mar 16, 2026
Full time
Quality Assurance (QA) Manager Medical Device manufacturer. Based Northern UK - M62 / M1 circa Manchester, Leeds, Sheffield, Doncaster Base salary £60-70k (Negotiable) with Bonus and Package. Role Overview Our client is a global medical device manufacturer seeking an experienced and hands-on Quality Assurance Manager to lead their Quality function in a regulated manufacturing environment. This role is ideal for a Quality professional from the medical device, pharmaceutical, or chemical manufacturing sectors who can operate strategically and practically - including close collaboration with laboratory teams to support QA testing and compliance. The QA Manager will ensure regulatory compliance, maintain a robust Quality Management System (QMS), and drive a culture of quality, safety, and continuous improvement across the business. Office access required 2-3 days a week. Key Responsibilities Quality Management & Compliance Lead, maintain, and continuously improve the QMS in line with: ISO 9001 ISO 14001 GMP standards (applicable to the sector) UK MDR (for medical device components, if applicable) Ensure audit readiness at all times and maintain accurate quality records. Manage document control, change control, and staff training compliance systems. Lead Management Review and report on key quality metrics and KPIs. One direct head reports into the QA Manager. Laboratory & Product Quality Oversight Work closely with laboratory teams to oversee QA testing processes. Ensure handling, testing, and documentation of products meet regulatory and safety standards. Integrate quality systems within lab operations to maintain data integrity, traceability, and compliance. Support method validation, stability studies, and product testing as required. GMP & Audit Leadership Lead internal and supplier audits, ensuring effective follow-up and closure of CAPAs. Prepare for and support external audits from certification bodies, MHRA, or other regulatory authorities. Implement and oversee GMP standards across production and laboratory operations. HACCP & Environmental Compliance Maintain and develop HACCP systems where relevant. Ensure environmental compliance aligned with ISO 14001 standards. Monitor and drive improvements in environmental, safety, and quality performance. Key Requirements Proven experience as a Quality Manager in medical device, pharmaceutical, or chemical manufacturing. Strong understanding of laboratory QA testing and ability to integrate with lab teams. Practical experience with: ISO 9001 ISO 14001 HACCP GMP standards Experience leading and managing internal and external audits. Strong knowledge of risk management, CAPA processes, and regulatory compliance. Excellent organisational, leadership, and communication skills. Personal Attributes Detail-oriented, proactive, and solutions-focused. Comfortable working strategically and hands-on. Confident engaging with auditors, regulators, and cross-functional teams. Committed to fostering a culture of compliance, accountability, and continuous improvement. Why Join? Leadership role with visible impact on quality, compliance, and operational excellence. Opportunity to work across multiple regulated sectors - medical device, pharmaceutical, and chemical manufacturing. Collaborative culture with close integration between lab, production, and operations. Competitive salary and benefits package.
Quality Assurance (QA) Manager Medical Device manufacturer. Based Northern UK - M62 / M1 circa Manchester, Leeds, Sheffield, Doncaster Base salary £60-70k (Negotiable) with Bonus and Package. Role Overview Our client is a global medical device manufacturer seeking an experienced and hands-on Quality Assurance Manager to lead their Quality function in a regulated manufacturing environment. This role is ideal for a Quality professional from the medical device, pharmaceutical, or chemical manufacturing sectors who can operate strategically and practically - including close collaboration with laboratory teams to support QA testing and compliance. The QA Manager will ensure regulatory compliance, maintain a robust Quality Management System (QMS), and drive a culture of quality, safety, and continuous improvement across the business. Office access required 2-3 days a week. Key Responsibilities Quality Management & Compliance Lead, maintain, and continuously improve the QMS in line with: ISO 9001 ISO 14001 GMP standards (applicable to the sector) UK MDR (for medical device components, if applicable) Ensure audit readiness at all times and maintain accurate quality records. Manage document control, change control, and staff training compliance systems. Lead Management Review and report on key quality metrics and KPIs. One direct head reports into the QA Manager. Laboratory & Product Quality Oversight Work closely with laboratory teams to oversee QA testing processes. Ensure handling, testing, and documentation of products meet regulatory and safety standards. Integrate quality systems within lab operations to maintain data integrity, traceability, and compliance. Support method validation, stability studies, and product testing as required. GMP & Audit Leadership Lead internal and supplier audits, ensuring effective follow-up and closure of CAPAs. Prepare for and support external audits from certification bodies, MHRA, or other regulatory authorities. Implement and oversee GMP standards across production and laboratory operations. HACCP & Environmental Compliance Maintain and develop HACCP systems where relevant. Ensure environmental compliance aligned with ISO 14001 standards. Monitor and drive improvements in environmental, safety, and quality performance. Key Requirements Proven experience as a Quality Manager in medical device, pharmaceutical, or chemical manufacturing. Strong understanding of laboratory QA testing and ability to integrate with lab teams. Practical experience with: ISO 9001 ISO 14001 HACCP GMP standards Experience leading and managing internal and external audits. Strong knowledge of risk management, CAPA processes, and regulatory compliance. Excellent organisational, leadership, and communication skills. Personal Attributes Detail-oriented, proactive, and solutions-focused. Comfortable working strategically and hands-on. Confident engaging with auditors, regulators, and cross-functional teams. Committed to fostering a culture of compliance, accountability, and continuous improvement. Why Join? Leadership role with visible impact on quality, compliance, and operational excellence. Opportunity to work across multiple regulated sectors - medical device, pharmaceutical, and chemical manufacturing. Collaborative culture with close integration between lab, production, and operations. Competitive salary and benefits package.
Mar 16, 2026
Full time
Quality Assurance (QA) Manager Medical Device manufacturer. Based Northern UK - M62 / M1 circa Manchester, Leeds, Sheffield, Doncaster Base salary £60-70k (Negotiable) with Bonus and Package. Role Overview Our client is a global medical device manufacturer seeking an experienced and hands-on Quality Assurance Manager to lead their Quality function in a regulated manufacturing environment. This role is ideal for a Quality professional from the medical device, pharmaceutical, or chemical manufacturing sectors who can operate strategically and practically - including close collaboration with laboratory teams to support QA testing and compliance. The QA Manager will ensure regulatory compliance, maintain a robust Quality Management System (QMS), and drive a culture of quality, safety, and continuous improvement across the business. Office access required 2-3 days a week. Key Responsibilities Quality Management & Compliance Lead, maintain, and continuously improve the QMS in line with: ISO 9001 ISO 14001 GMP standards (applicable to the sector) UK MDR (for medical device components, if applicable) Ensure audit readiness at all times and maintain accurate quality records. Manage document control, change control, and staff training compliance systems. Lead Management Review and report on key quality metrics and KPIs. One direct head reports into the QA Manager. Laboratory & Product Quality Oversight Work closely with laboratory teams to oversee QA testing processes. Ensure handling, testing, and documentation of products meet regulatory and safety standards. Integrate quality systems within lab operations to maintain data integrity, traceability, and compliance. Support method validation, stability studies, and product testing as required. GMP & Audit Leadership Lead internal and supplier audits, ensuring effective follow-up and closure of CAPAs. Prepare for and support external audits from certification bodies, MHRA, or other regulatory authorities. Implement and oversee GMP standards across production and laboratory operations. HACCP & Environmental Compliance Maintain and develop HACCP systems where relevant. Ensure environmental compliance aligned with ISO 14001 standards. Monitor and drive improvements in environmental, safety, and quality performance. Key Requirements Proven experience as a Quality Manager in medical device, pharmaceutical, or chemical manufacturing. Strong understanding of laboratory QA testing and ability to integrate with lab teams. Practical experience with: ISO 9001 ISO 14001 HACCP GMP standards Experience leading and managing internal and external audits. Strong knowledge of risk management, CAPA processes, and regulatory compliance. Excellent organisational, leadership, and communication skills. Personal Attributes Detail-oriented, proactive, and solutions-focused. Comfortable working strategically and hands-on. Confident engaging with auditors, regulators, and cross-functional teams. Committed to fostering a culture of compliance, accountability, and continuous improvement. Why Join? Leadership role with visible impact on quality, compliance, and operational excellence. Opportunity to work across multiple regulated sectors - medical device, pharmaceutical, and chemical manufacturing. Collaborative culture with close integration between lab, production, and operations. Competitive salary and benefits package.
Are you an experienced Quality Assurance Leader looking for a challenge with a really exciting CDMO focused on Pharmaceutical Manufacturing? Job Title: Quality Assurance Manager Type: Permanent Salary: Highly attractive Location: Northwest, England SRG is currently working exclusively with a highly successful, award winning, contract development and manufacturing organisation focused on providing expert intelligence and support to their partners, driven by their capabilities. As a result of expansion, we are looking for a Quality Assurance Manager to join their quality team. Typical responsibilities/accountabilities: Ensure full compliance with UK/EU GMP Regulatory Standards and company procedures. Lead and manage the Quality Assurance Team at an IMP manufacturing site, focused on Phase I and Phase II clinical trial materials. Maintain QA systems and processes, reviewing and supporting ongoing improvement activities. Ensure effective management of documents through life-cycle, ensuring compliance with regulations and industry best practices. This includes - creating, reviewing, and approving key documentation such as specifications, SOPs, protocols, and methods associated with all products and procedures. Support batch documentation review and provide quality oversight for the certification and release of IMPs by the QP. Investigating and approval of deviations, complaints and OOS to prevent future re-occurrences of non-conformance, providing support on SMART CAPA plans. Supplier Management: Managing supplier approval and ongoing performance. Evaluating site compliance and implementing improvements through the internal audit process, as an Internal Auditor and Report approver. Supporting Client projects as a Quality Assurance representative and Customer liaison Support generation and cascade of quality training packages, including but not limited to GMP induction and annual refresher. Assist with management of Regulatory inspections: inspection readiness, inspection and response. Essential Requirements: Proven Leadership/ Management experience in Quality Assurance within a Pharmaceutical (GMP) facility. Degree or equivalent in a relevant scientific discipline Experience in working with analytical laboratories and/ or GMP production areas. Experience with Investigational Medicinal Products (IMPs) would be advantageous. SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients. If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit (url removed) to view our other vacancies. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.
Mar 14, 2026
Full time
Are you an experienced Quality Assurance Leader looking for a challenge with a really exciting CDMO focused on Pharmaceutical Manufacturing? Job Title: Quality Assurance Manager Type: Permanent Salary: Highly attractive Location: Northwest, England SRG is currently working exclusively with a highly successful, award winning, contract development and manufacturing organisation focused on providing expert intelligence and support to their partners, driven by their capabilities. As a result of expansion, we are looking for a Quality Assurance Manager to join their quality team. Typical responsibilities/accountabilities: Ensure full compliance with UK/EU GMP Regulatory Standards and company procedures. Lead and manage the Quality Assurance Team at an IMP manufacturing site, focused on Phase I and Phase II clinical trial materials. Maintain QA systems and processes, reviewing and supporting ongoing improvement activities. Ensure effective management of documents through life-cycle, ensuring compliance with regulations and industry best practices. This includes - creating, reviewing, and approving key documentation such as specifications, SOPs, protocols, and methods associated with all products and procedures. Support batch documentation review and provide quality oversight for the certification and release of IMPs by the QP. Investigating and approval of deviations, complaints and OOS to prevent future re-occurrences of non-conformance, providing support on SMART CAPA plans. Supplier Management: Managing supplier approval and ongoing performance. Evaluating site compliance and implementing improvements through the internal audit process, as an Internal Auditor and Report approver. Supporting Client projects as a Quality Assurance representative and Customer liaison Support generation and cascade of quality training packages, including but not limited to GMP induction and annual refresher. Assist with management of Regulatory inspections: inspection readiness, inspection and response. Essential Requirements: Proven Leadership/ Management experience in Quality Assurance within a Pharmaceutical (GMP) facility. Degree or equivalent in a relevant scientific discipline Experience in working with analytical laboratories and/ or GMP production areas. Experience with Investigational Medicinal Products (IMPs) would be advantageous. SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients. If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit (url removed) to view our other vacancies. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.
Quality Auditor Salary: Competitive salary Benefits: Company share save scheme, Competitive matched pension contributions, Life insurance up to 4x salary Location: Highbridge, TA9 4JR Ways of Working: Site Based Hours of work: 4 on 4 off rotating shift (Day shift 06:00-18:00 2 consecutive shifts) (Night shift 18:00-06:00 2 consecuctive shifts) Contract Type: Permanent Why Greencore? Following the combination with Bakkavor in January 2026, we're one of the UK's leading creators of convenience food, driven by a simple purpose: to make every day taste better. As a vibrant and fast-moving business, we're proud to employ over 28,000 talented colleagues across 36 manufacturing sites and 21 distribution depots in the UK and the US. Together, we bring delicious food to life. Our products cover every meal occasion from breakfast through to dinner and dessert, with lunch and snacking in between. In FY25, our shared passion helped us achieve combined revenues of approximately £4bn. Our extensive direct to store (DTS) network, with 17 depots across the UK, allows us to deliver fresh and frozen food, both our own and from trusted partners, to thousands of stores every day, ensuring consumers enjoy the very best, whenever and wherever they shop. Our Bakkavor site in Highbridge, which is one of our four Desserts sites in the UK, specialises in Cheesecake and Tarts, working closely with our sister site in Devizes that specialise in baked goods. What you'll be doing 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 standards in line with Greencore, customer, and legal requirements, with guidance from the QA Supervisor or Manager. Role Accountabilities • Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure • Apply an inquisitive audit mindset to identify root causes and reduce repeat non-conformances • Conduct traceability audits, efficiently retrieving data and presenting findings clearly • Complete sampling activities to schedule, including microbiological, nutritional, swabs, and organoleptic testing • Prepare, facilitate, and trend taste panels, escalating out-of-specification results and recommending improvements • Calibrate factory measurement equipment to schedule and manage out-of-tolerance actions • Support investigations into complaints, incidents, and out-of-specification results through audits and data analysis • Support NPD trials and product launches, including testing, shelf-life assessment, and taste panels • Provide day-to-day technical support to factory teams, audits, and customer visits • Contribute to Technical KPI delivery through audits, investigations, and proactive improvement actions • Work safely at all times, promoting strong health, safety, and environmental standards What we're looking for • A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment • A proactive, detail-focused approach with a natural curiosity to challenge and improve standards • Confidence working hands-on on the factory floor, providing clear and practical technical guidance • Ability to audit effectively, identify root causes, and drive corrective and preventative actions • Strong communication skills, able to engage confidently with colleagues at all levels • A collaborative mindset, working effectively within cross-functional teams • Good organisational skills, with the ability to manage multiple priorities to deadlines • Commitment to continuous improvement and personal development • A positive, resilient approach aligned to Greencore values We're not all the same at Greencore and our differences help us to make every day taste better for all our stakeholders. We truly put our people at the core and are proud of our diversity. If this sounds like you, join us and grow with Greencore, and be a part of driving our future success. What you'll get in return • Competitive salary and job-related benefits • Holidays • Competitive matched pension contributions • Life insurance up to 4x salary • Company share save scheme • Greencore Qualifications • Exclusive Greencore employee discount platform • Access to a full Wellbeing Centre platform • Enhanced parental leave and menopause policies Throughout your time at Greencore, you will be supported with on-the-job training and development opportunities to further your career.
Mar 14, 2026
Full time
Quality Auditor Salary: Competitive salary Benefits: Company share save scheme, Competitive matched pension contributions, Life insurance up to 4x salary Location: Highbridge, TA9 4JR Ways of Working: Site Based Hours of work: 4 on 4 off rotating shift (Day shift 06:00-18:00 2 consecutive shifts) (Night shift 18:00-06:00 2 consecuctive shifts) Contract Type: Permanent Why Greencore? Following the combination with Bakkavor in January 2026, we're one of the UK's leading creators of convenience food, driven by a simple purpose: to make every day taste better. As a vibrant and fast-moving business, we're proud to employ over 28,000 talented colleagues across 36 manufacturing sites and 21 distribution depots in the UK and the US. Together, we bring delicious food to life. Our products cover every meal occasion from breakfast through to dinner and dessert, with lunch and snacking in between. In FY25, our shared passion helped us achieve combined revenues of approximately £4bn. Our extensive direct to store (DTS) network, with 17 depots across the UK, allows us to deliver fresh and frozen food, both our own and from trusted partners, to thousands of stores every day, ensuring consumers enjoy the very best, whenever and wherever they shop. Our Bakkavor site in Highbridge, which is one of our four Desserts sites in the UK, specialises in Cheesecake and Tarts, working closely with our sister site in Devizes that specialise in baked goods. What you'll be doing 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 standards in line with Greencore, customer, and legal requirements, with guidance from the QA Supervisor or Manager. Role Accountabilities • Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure • Apply an inquisitive audit mindset to identify root causes and reduce repeat non-conformances • Conduct traceability audits, efficiently retrieving data and presenting findings clearly • Complete sampling activities to schedule, including microbiological, nutritional, swabs, and organoleptic testing • Prepare, facilitate, and trend taste panels, escalating out-of-specification results and recommending improvements • Calibrate factory measurement equipment to schedule and manage out-of-tolerance actions • Support investigations into complaints, incidents, and out-of-specification results through audits and data analysis • Support NPD trials and product launches, including testing, shelf-life assessment, and taste panels • Provide day-to-day technical support to factory teams, audits, and customer visits • Contribute to Technical KPI delivery through audits, investigations, and proactive improvement actions • Work safely at all times, promoting strong health, safety, and environmental standards What we're looking for • A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment • A proactive, detail-focused approach with a natural curiosity to challenge and improve standards • Confidence working hands-on on the factory floor, providing clear and practical technical guidance • Ability to audit effectively, identify root causes, and drive corrective and preventative actions • Strong communication skills, able to engage confidently with colleagues at all levels • A collaborative mindset, working effectively within cross-functional teams • Good organisational skills, with the ability to manage multiple priorities to deadlines • Commitment to continuous improvement and personal development • A positive, resilient approach aligned to Greencore values We're not all the same at Greencore and our differences help us to make every day taste better for all our stakeholders. We truly put our people at the core and are proud of our diversity. If this sounds like you, join us and grow with Greencore, and be a part of driving our future success. What you'll get in return • Competitive salary and job-related benefits • Holidays • Competitive matched pension contributions • Life insurance up to 4x salary • Company share save scheme • Greencore Qualifications • Exclusive Greencore employee discount platform • Access to a full Wellbeing Centre platform • Enhanced parental leave and menopause policies Throughout your time at Greencore, you will be supported with on-the-job training and development opportunities to further your career.
QA Manager The Role We are recruiting a QA Manager to join a well-established fresh food manufacturing business. Reporting to the Technical Manager, this is a hands-on, site-based role responsible for maintaining food safety, quality, legality and authenticity across the operation. You will lead the QA team on shift, maintain audit readiness and act as a visible quality champion on the shop floor. Working closely with Operations, Hygiene, Engineering and Technical teams, you will support compliance with customer, retailer and legislative standards while driving continuous improvement. Key Responsibilities Lead and develop the QA team and support training and capability building Manage product on hold and release decisions, escalating where required Support internal and external audits and maintain audit readiness Monitor GMP, hygiene and factory standards and drive corrective actions Reduce non-conformances, customer complaints and product rejections Maintain full traceability and support QA systems and documentation Support root cause investigations and continuous improvement activity About You Experience in a QA or Technical role within fresh food manufacturing Strong knowledge of food safety legislation and QA systems Experience supervising or leading QA teams Confident making product release decisions in a fast-paced environment Organised, proactive and comfortable working on the shop floor Essential Qualifications Level 3 HACCP Level 3 Food Safety and Hygiene Internal Auditor training or willingness to complete Interested? For further information, please get in touch with Oskar Ballard at MorePeople on (phone number removed) or email (url removed)
Mar 13, 2026
Full time
QA Manager The Role We are recruiting a QA Manager to join a well-established fresh food manufacturing business. Reporting to the Technical Manager, this is a hands-on, site-based role responsible for maintaining food safety, quality, legality and authenticity across the operation. You will lead the QA team on shift, maintain audit readiness and act as a visible quality champion on the shop floor. Working closely with Operations, Hygiene, Engineering and Technical teams, you will support compliance with customer, retailer and legislative standards while driving continuous improvement. Key Responsibilities Lead and develop the QA team and support training and capability building Manage product on hold and release decisions, escalating where required Support internal and external audits and maintain audit readiness Monitor GMP, hygiene and factory standards and drive corrective actions Reduce non-conformances, customer complaints and product rejections Maintain full traceability and support QA systems and documentation Support root cause investigations and continuous improvement activity About You Experience in a QA or Technical role within fresh food manufacturing Strong knowledge of food safety legislation and QA systems Experience supervising or leading QA teams Confident making product release decisions in a fast-paced environment Organised, proactive and comfortable working on the shop floor Essential Qualifications Level 3 HACCP Level 3 Food Safety and Hygiene Internal Auditor training or willingness to complete Interested? For further information, please get in touch with Oskar Ballard at MorePeople on (phone number removed) or email (url removed)
Product Quality Assurance Manager The Role We are recruiting a Product Quality Assurance Manager responsible for overseeing product quality, food safety, legality, and integrity across a soft fruit operation, ensuring compliance with customer, retailer, and legislative standards. This role requires a hands-on quality professional with strong communication skills and the ability to work closely with production, harvest, commercial, and technical teams to manage quality performance and resolve issues efficiently. You will play a key role in maintaining high product standards from field to customer in a fast-paced fresh produce environment. Key Responsibilities Quality Assurance & Compliance Ensure all products meet required food safety, legal, integrity, and customer standards Deliver Quality Service Level (QSL) targets for the business and customers Investigate complaints, rejections, and non-conformances, ensuring timely resolution Maintain and improve QA systems in line with BRCGS v9 and retailer requirements Analyse and trend quality data to drive continuous improvement Team Leadership & Development Manage and develop QA and Label Room teams Ensure customer specifications and quality standards are consistently met Promote a right first time culture across production teams Manage the QA budget and support effective resource planning Cross-Functional & Customer Support Work closely with commercial, production, and operational teams to resolve quality issues Support customer visits and technical discussions Build strong relationships with internal and external stakeholders Auditing & Site Engagement Carry out internal and external quality visits Document findings and communicate outcomes to relevant stakeholders Support audit readiness and ongoing compliance activity Contribute to internal initiatives and continuous improvement projects About You Experience in a Quality or Technical role within Fresh Produce Strong knowledge of BRCGS v9, retailer standards, and food safety systems HACCP Level 2 and Food Safety Level 2 TACCP/VACCP training and Lead Auditor training preferred Experience leading or supervising QA teams Confident communicating with customers and internal teams Strong analytical, problem-solving, and IT skills Proactive, detail-focused, and comfortable working in a fast-paced environment Need to have a legal right to work in the UK For further information, please get in touch with Oskar Ballard at MorePeople on (phone number removed) or email (url removed)
Mar 13, 2026
Full time
Product Quality Assurance Manager The Role We are recruiting a Product Quality Assurance Manager responsible for overseeing product quality, food safety, legality, and integrity across a soft fruit operation, ensuring compliance with customer, retailer, and legislative standards. This role requires a hands-on quality professional with strong communication skills and the ability to work closely with production, harvest, commercial, and technical teams to manage quality performance and resolve issues efficiently. You will play a key role in maintaining high product standards from field to customer in a fast-paced fresh produce environment. Key Responsibilities Quality Assurance & Compliance Ensure all products meet required food safety, legal, integrity, and customer standards Deliver Quality Service Level (QSL) targets for the business and customers Investigate complaints, rejections, and non-conformances, ensuring timely resolution Maintain and improve QA systems in line with BRCGS v9 and retailer requirements Analyse and trend quality data to drive continuous improvement Team Leadership & Development Manage and develop QA and Label Room teams Ensure customer specifications and quality standards are consistently met Promote a right first time culture across production teams Manage the QA budget and support effective resource planning Cross-Functional & Customer Support Work closely with commercial, production, and operational teams to resolve quality issues Support customer visits and technical discussions Build strong relationships with internal and external stakeholders Auditing & Site Engagement Carry out internal and external quality visits Document findings and communicate outcomes to relevant stakeholders Support audit readiness and ongoing compliance activity Contribute to internal initiatives and continuous improvement projects About You Experience in a Quality or Technical role within Fresh Produce Strong knowledge of BRCGS v9, retailer standards, and food safety systems HACCP Level 2 and Food Safety Level 2 TACCP/VACCP training and Lead Auditor training preferred Experience leading or supervising QA teams Confident communicating with customers and internal teams Strong analytical, problem-solving, and IT skills Proactive, detail-focused, and comfortable working in a fast-paced environment Need to have a legal right to work in the UK For further information, please get in touch with Oskar Ballard at MorePeople on (phone number removed) or email (url removed)
Claims Governance & Best Practice Manager Location: Manchester/ Chelmsford/ Whitstable/ Tunbridge Wells / Haywards Heath (Hybrid) The Opportunity We are looking for an experienced and technically strong Claims Governance & Best Practice Manager to lead the governance framework across our claims function. This is a senior role with strategic influence, responsible for ensuring governance, documentation, and best practice across the claims organisation remain robust, compliant, and aligned to regulatory expectations. Working closely with Claims Operations, Compliance, Risk, Audit and senior stakeholders, you will ensure governance standards are embedded across the business while driving continuous improvement in technical quality and operational excellence. If you enjoy combining technical claims expertise, governance leadership and strategic thinking , this role offers the chance to shape best practice across a large and evolving claims function. What You Will Be Doing Governance Leadership Own and maintain the Claims Governance Framework across all lines of business Oversee adherence to governance standards and regulatory obligations across the claims function Lead governance of best practice materials, claims documentation and strategy documentation Ensure strong version control, approvals and lifecycle management for all governance materials Support operational resilience and ensure robust governance controls remain in place Technical Best Practice Act as the senior authority on claims best practice Drive improvements in processes, procedures and governance controls Provide governance input into transformation initiatives, systems changes and improvement programmes Leadership Lead and develop the Claims Document Governance team Embed a high performing culture focused on strong customer outcomes Oversee team prioritisation, workload management and delivery against agreed service levels Risk, Quality and Insight Produce monthly governance reporting and management insight Identify trends, risks and opportunities for improvement Support internal and external audit activity and ensure governance evidence supports Consumer Duty expectations Stakeholder Collaboration Act as a central governance partner across the claims business Work closely with QA, Risk, Audit and Compliance teams Engage with suppliers, partners and external auditors where required What We Are Looking For Essential Experience Extensive insurance claims experience with strong technical knowledge across Motor claims including Personal Injury, Credit Hire and Property Damage Strong understanding of claims governance, regulatory expectations and compliance frameworks Experience leading a technical or governance function Proven ability to influence senior stakeholders across a large organisation Experience managing external audits within a claims environment Strong analytical capability with experience using management information to drive insight Excellent communication skills with the ability to simplify complex technical material Project or change management experience Desirable Dip CII or equivalent qualification Experience working with automated decision making or AI assisted claims handling Knowledge of operational resilience frameworks Experience working within audit or risk assurance environments Familiarity with Agile change delivery Why Join This role offers a genuine opportunity to shape the governance standards and technical excellence of a major claims operation . You will work with senior leaders across the organisation while building a culture that prioritises strong governance, fair customer outcomes and continuous improvement. If you are an experienced claims professional with a passion for governance, technical excellence and leadership, we would love to hear from you.
Mar 05, 2026
Full time
Claims Governance & Best Practice Manager Location: Manchester/ Chelmsford/ Whitstable/ Tunbridge Wells / Haywards Heath (Hybrid) The Opportunity We are looking for an experienced and technically strong Claims Governance & Best Practice Manager to lead the governance framework across our claims function. This is a senior role with strategic influence, responsible for ensuring governance, documentation, and best practice across the claims organisation remain robust, compliant, and aligned to regulatory expectations. Working closely with Claims Operations, Compliance, Risk, Audit and senior stakeholders, you will ensure governance standards are embedded across the business while driving continuous improvement in technical quality and operational excellence. If you enjoy combining technical claims expertise, governance leadership and strategic thinking , this role offers the chance to shape best practice across a large and evolving claims function. What You Will Be Doing Governance Leadership Own and maintain the Claims Governance Framework across all lines of business Oversee adherence to governance standards and regulatory obligations across the claims function Lead governance of best practice materials, claims documentation and strategy documentation Ensure strong version control, approvals and lifecycle management for all governance materials Support operational resilience and ensure robust governance controls remain in place Technical Best Practice Act as the senior authority on claims best practice Drive improvements in processes, procedures and governance controls Provide governance input into transformation initiatives, systems changes and improvement programmes Leadership Lead and develop the Claims Document Governance team Embed a high performing culture focused on strong customer outcomes Oversee team prioritisation, workload management and delivery against agreed service levels Risk, Quality and Insight Produce monthly governance reporting and management insight Identify trends, risks and opportunities for improvement Support internal and external audit activity and ensure governance evidence supports Consumer Duty expectations Stakeholder Collaboration Act as a central governance partner across the claims business Work closely with QA, Risk, Audit and Compliance teams Engage with suppliers, partners and external auditors where required What We Are Looking For Essential Experience Extensive insurance claims experience with strong technical knowledge across Motor claims including Personal Injury, Credit Hire and Property Damage Strong understanding of claims governance, regulatory expectations and compliance frameworks Experience leading a technical or governance function Proven ability to influence senior stakeholders across a large organisation Experience managing external audits within a claims environment Strong analytical capability with experience using management information to drive insight Excellent communication skills with the ability to simplify complex technical material Project or change management experience Desirable Dip CII or equivalent qualification Experience working with automated decision making or AI assisted claims handling Knowledge of operational resilience frameworks Experience working within audit or risk assurance environments Familiarity with Agile change delivery Why Join This role offers a genuine opportunity to shape the governance standards and technical excellence of a major claims operation . You will work with senior leaders across the organisation while building a culture that prioritises strong governance, fair customer outcomes and continuous improvement. If you are an experienced claims professional with a passion for governance, technical excellence and leadership, we would love to hear from you.
Job Title: Quality Assurance Supervisor Location: Tarleton, PR4 6LJ Salary: Up to 35,000 per year Job type: Permanent, Full-time. Monday to Friday. This role offers flexible working hours to meet the requirements of both the business and the employee. Bryans Salads are currently recruiting for a passionate Quality Assurance Supervisor to join our rapidly expanding site in Tarleton, PR4 6LJ. About Bryan's Salads: Bryans Salads Ltd is a third-generation family business based in the rural moss lands of Tarleton, Lancashire. We specialize in washed, ready-to-eat sliced lettuce and salad leaf, and we also produce high-quality ready-to-cook vegetable packs and salad bowls (with or without added protein) for the catering and food service industry. About the Role: We are looking for a dedicated QA Supervisor to join our expanding team. This role is critical in ensuring that all products meet the highest standards of quality, safety, and compliance. The QA Supervisor will oversee daily quality assurance activities on site, supporting and guiding a team of QA Assistants, maintaining compliance with customer and industry standards, and driving continuous improvements across the site. Food production experience is essential. Experience with fresh produce will be considered a strong advantage. Key Responsibilities: Supervise and support the QA team, ensuring consistent performance and training. Monitor product quality and take action to address non-conformances. Maintain compliance with BRCGS standards, customer codes of practice, and industry legislation. Conduct gap analyses and implement improvement plans. Assist with training, ensuring company policies and procedures are effectively communicated. Actively participate in HACCP meetings and support with documentation updates. Lead and support internal and external audits. Analyse quality and technical data, providing reports and corrective actions as required. Knowledge & Specific Job Skills: Essential; Level 3 HACCP and Level 3 Food Safety Internal Auditing training Understanding of food microbiology and allergens management Experience maintaining a Quality Management System (QMS) to BRC standards Strong Excel/data analysis skills Desirable; Experience in fresh produce or chilled food manufacturing Benefits: Life insurance Company pension Free on-site parking Canteen access Casual dress Please click on the APPLY button to send your CV for this role. Candidates with the relevant experience or job titles of; ISO 9001, Quality, Quality Inspector, Quality Assessor, Quality Manager, Quality Management Systems, Auditor, Security Auditor, Fire Inspector, Fire and Security Officer, Fire and Security Auditor, Compliance, Health and Safety, Security, Compliance Administrator, Compliance Coordinator, Compliance Officer, Compliance Advisor, Compliance Handler, Compliance Specialist, EHS, EHSQ, Quality Administrator, Quality Coordinator, Quality Control, Project Coordinator, Health and Safety Manager, Health and Safety Administrator, Health and Safety Coordinator, will also be considered for this role.
Oct 08, 2025
Full time
Job Title: Quality Assurance Supervisor Location: Tarleton, PR4 6LJ Salary: Up to 35,000 per year Job type: Permanent, Full-time. Monday to Friday. This role offers flexible working hours to meet the requirements of both the business and the employee. Bryans Salads are currently recruiting for a passionate Quality Assurance Supervisor to join our rapidly expanding site in Tarleton, PR4 6LJ. About Bryan's Salads: Bryans Salads Ltd is a third-generation family business based in the rural moss lands of Tarleton, Lancashire. We specialize in washed, ready-to-eat sliced lettuce and salad leaf, and we also produce high-quality ready-to-cook vegetable packs and salad bowls (with or without added protein) for the catering and food service industry. About the Role: We are looking for a dedicated QA Supervisor to join our expanding team. This role is critical in ensuring that all products meet the highest standards of quality, safety, and compliance. The QA Supervisor will oversee daily quality assurance activities on site, supporting and guiding a team of QA Assistants, maintaining compliance with customer and industry standards, and driving continuous improvements across the site. Food production experience is essential. Experience with fresh produce will be considered a strong advantage. Key Responsibilities: Supervise and support the QA team, ensuring consistent performance and training. Monitor product quality and take action to address non-conformances. Maintain compliance with BRCGS standards, customer codes of practice, and industry legislation. Conduct gap analyses and implement improvement plans. Assist with training, ensuring company policies and procedures are effectively communicated. Actively participate in HACCP meetings and support with documentation updates. Lead and support internal and external audits. Analyse quality and technical data, providing reports and corrective actions as required. Knowledge & Specific Job Skills: Essential; Level 3 HACCP and Level 3 Food Safety Internal Auditing training Understanding of food microbiology and allergens management Experience maintaining a Quality Management System (QMS) to BRC standards Strong Excel/data analysis skills Desirable; Experience in fresh produce or chilled food manufacturing Benefits: Life insurance Company pension Free on-site parking Canteen access Casual dress Please click on the APPLY button to send your CV for this role. Candidates with the relevant experience or job titles of; ISO 9001, Quality, Quality Inspector, Quality Assessor, Quality Manager, Quality Management Systems, Auditor, Security Auditor, Fire Inspector, Fire and Security Officer, Fire and Security Auditor, Compliance, Health and Safety, Security, Compliance Administrator, Compliance Coordinator, Compliance Officer, Compliance Advisor, Compliance Handler, Compliance Specialist, EHS, EHSQ, Quality Administrator, Quality Coordinator, Quality Control, Project Coordinator, Health and Safety Manager, Health and Safety Administrator, Health and Safety Coordinator, will also be considered for this role.
Job Title: QA Location: Spalding Salary: 28,000 - 29,000 Ref: AM20096 Are you passionate about food quality and wanting a new opportunity? If so, we want to hear from you. We are working with an award-winning food business, that supplies premium product to many of the retailers. They are looking for passionate Quality Auditor to come and join the team. As Quality Auditor you will work closely with all teams to ensure that all product is produced as per customer specifications. Complete quality records daily or against the agreed frequency detailed in the product specification. Daily completion of quality start up and completion checks. Daily production quality checks such as torque tests and product weight checks, paperwork checks, ensuring all batch codes and dates are entered and correct. This will suit a food manufacturing QC QA who can make decisions on quality, has good knowledge of HACCP and sampling practices, excellent communication at all levels and able to manage and work effectively within a busy team. Good IT skills are essential and full driving licence are also needed. If this sounds like you, please apply via the link. Alternatively, for a confidential chat about the role, please contact Alex on (phone number removed) or (url removed). INDTECH
Oct 07, 2025
Full time
Job Title: QA Location: Spalding Salary: 28,000 - 29,000 Ref: AM20096 Are you passionate about food quality and wanting a new opportunity? If so, we want to hear from you. We are working with an award-winning food business, that supplies premium product to many of the retailers. They are looking for passionate Quality Auditor to come and join the team. As Quality Auditor you will work closely with all teams to ensure that all product is produced as per customer specifications. Complete quality records daily or against the agreed frequency detailed in the product specification. Daily completion of quality start up and completion checks. Daily production quality checks such as torque tests and product weight checks, paperwork checks, ensuring all batch codes and dates are entered and correct. This will suit a food manufacturing QC QA who can make decisions on quality, has good knowledge of HACCP and sampling practices, excellent communication at all levels and able to manage and work effectively within a busy team. Good IT skills are essential and full driving licence are also needed. If this sounds like you, please apply via the link. Alternatively, for a confidential chat about the role, please contact Alex on (phone number removed) or (url removed). INDTECH
Sector: Nuclear Duties: Provide and demonstrate positive leadership, building a strong and compliant culture Ensure all site activities are undertaken safely and responsibly Support the Quality Manager in capturing the changes to Quality requirements in contract requirements mapping/capture process Maintaining and updating the Contract Quality Assurance Plan (CQAP) Assist in managing the Quality Management System (QMS) of the project Ensure the communication, training and implementation of the QMS within the team Monitor and measure the efficiency of the QMS and ensure improvement of the QMS Assist in preparing audit planning, performing audits (including supplier assessment audits), follow up sentencing of findings and progress of action plans Co-ordinate preparations for external audits and follow up sentencing of findings and progress of action plans Qualifications: Qualified ISO 9001:2015 Lead auditor with experience auditing to the standard Good understanding of inspection processes and protocols Understand the concepts and applications of problem solving and improvement tools. Competent in producing, tracking and analysing quality key performance indicators (KPIs) and creating QA Dashboards. Degree qualified or minimum 3 years Quality Engineering experience within a regulated industry Experience in Quality Tools (6 Sigma / 8D / RCA). Proficiency developing and reviewing QA-related procedures, templates and forms, with a solid grasp of QA best practices. Understanding of document management systems.
Oct 07, 2025
Full time
Sector: Nuclear Duties: Provide and demonstrate positive leadership, building a strong and compliant culture Ensure all site activities are undertaken safely and responsibly Support the Quality Manager in capturing the changes to Quality requirements in contract requirements mapping/capture process Maintaining and updating the Contract Quality Assurance Plan (CQAP) Assist in managing the Quality Management System (QMS) of the project Ensure the communication, training and implementation of the QMS within the team Monitor and measure the efficiency of the QMS and ensure improvement of the QMS Assist in preparing audit planning, performing audits (including supplier assessment audits), follow up sentencing of findings and progress of action plans Co-ordinate preparations for external audits and follow up sentencing of findings and progress of action plans Qualifications: Qualified ISO 9001:2015 Lead auditor with experience auditing to the standard Good understanding of inspection processes and protocols Understand the concepts and applications of problem solving and improvement tools. Competent in producing, tracking and analysing quality key performance indicators (KPIs) and creating QA Dashboards. Degree qualified or minimum 3 years Quality Engineering experience within a regulated industry Experience in Quality Tools (6 Sigma / 8D / RCA). Proficiency developing and reviewing QA-related procedures, templates and forms, with a solid grasp of QA best practices. Understanding of document management systems.
We are currently recruiting for a Product Quality Engineer on a permanent basis to join TKMS ATLAS UK based in Winfrith Newburgh, Dorset. TKMS ATLAS UK develop, supply and support cutting-edge maritime technology for customers worldwide. They are offering flexible working, and an opportunity to work with like minded people. As a Product Quality Engineer, you will provide assurance to the company and customers that the appropriate QA requirements are being met including necessary quality control activities throughout the design, development and delivery of complex products. You will work closely with all internal stakeholders ensuring product conformity, regulatory standards and records are maintained. Key responsibilities include: • Provide independent assessment of lifecycle design review inputs, entry and exit criteria • Responsibility for independent authority during validation and verification activities • Ownership to closure of all product related issues both internally and externally including Customer issues • Revising and updating process and implementation to reduce risk of non-conformance issues • Complete quality audits and surveillance activities • Ownership of effective close out of internal and external audit findings • Perform proactive and regular operational activity surveillance promoting both best practice as well as highlighting areas for improvement with a view to minimising the likelihood of quality escapes • Ensuring all product records are maintained effectively to ensure configuration is maintained throughout product lifecycle • Articulate issues, provide constructive feedback and advocate for quality standards • Production and maintenance of contracted Quality deliverables. • Act as a conduit between Engineering and Production to ensure engineering assurance on delivered products. • Generate and update of Quality Management Plans Qualifications and skills • Relevant work experience in similar quality related role • Quality business system management system auditor • Proficient in Root Cause Analysis • Strong understanding of configuration management With a reputation for providing innovative underwater systems for the Royal Navy (RN) and export customers, TKMS ATLAS UK operates from our Headquarters on the Jurassic Coast in Dorset. Through science, engineering and R&D we convert data into information, knowledge and capabilities that challenge the status quo, and offer winning advantage at the frontline. Our people are at the heart of our success, an open and stimulating workspace empowers and encourages our people to be creative and act with integrity. Despite our continued growth, TKMS ATLAS UK pride ourselves on retaining a friendly and welcoming culture. As well as boasting a substantial benefits package, we offer progression and personal development opportunities, competitive remuneration, flexible working and a generous pension scheme. The continuous investment in our unique in-house test and integration facilities has supported TKMS ATLAS UK s growth in supplying UK and global markets with submarine and ship systems. This includes sonar, autonomous systems, marine electric actuation and mine counter-measures. Our Portland Harbour waterside facilities provide an excellent environment to test systems at sea. As a leading innovative maritime systems company, TKMS ATLAS UK operate throughout all phases of the acquisition and engineering lifecycles, from concept to In-service Support. • Competitive salary • Career Development and Training • 25 days holiday (increasing to 28 days after 5 years employment and 30 days after 10 years) • Dental Cover and Employee Assistance Programme • Flexible working patterns At TKMS ATLAS UK, we support our staff to create work-life balance and encourage applications from individuals who are looking for part time or condensed hours as well as full time opportunities. The successful candidate must be able to achieve full SC (Security Clearance).
Oct 07, 2025
Full time
We are currently recruiting for a Product Quality Engineer on a permanent basis to join TKMS ATLAS UK based in Winfrith Newburgh, Dorset. TKMS ATLAS UK develop, supply and support cutting-edge maritime technology for customers worldwide. They are offering flexible working, and an opportunity to work with like minded people. As a Product Quality Engineer, you will provide assurance to the company and customers that the appropriate QA requirements are being met including necessary quality control activities throughout the design, development and delivery of complex products. You will work closely with all internal stakeholders ensuring product conformity, regulatory standards and records are maintained. Key responsibilities include: • Provide independent assessment of lifecycle design review inputs, entry and exit criteria • Responsibility for independent authority during validation and verification activities • Ownership to closure of all product related issues both internally and externally including Customer issues • Revising and updating process and implementation to reduce risk of non-conformance issues • Complete quality audits and surveillance activities • Ownership of effective close out of internal and external audit findings • Perform proactive and regular operational activity surveillance promoting both best practice as well as highlighting areas for improvement with a view to minimising the likelihood of quality escapes • Ensuring all product records are maintained effectively to ensure configuration is maintained throughout product lifecycle • Articulate issues, provide constructive feedback and advocate for quality standards • Production and maintenance of contracted Quality deliverables. • Act as a conduit between Engineering and Production to ensure engineering assurance on delivered products. • Generate and update of Quality Management Plans Qualifications and skills • Relevant work experience in similar quality related role • Quality business system management system auditor • Proficient in Root Cause Analysis • Strong understanding of configuration management With a reputation for providing innovative underwater systems for the Royal Navy (RN) and export customers, TKMS ATLAS UK operates from our Headquarters on the Jurassic Coast in Dorset. Through science, engineering and R&D we convert data into information, knowledge and capabilities that challenge the status quo, and offer winning advantage at the frontline. Our people are at the heart of our success, an open and stimulating workspace empowers and encourages our people to be creative and act with integrity. Despite our continued growth, TKMS ATLAS UK pride ourselves on retaining a friendly and welcoming culture. As well as boasting a substantial benefits package, we offer progression and personal development opportunities, competitive remuneration, flexible working and a generous pension scheme. The continuous investment in our unique in-house test and integration facilities has supported TKMS ATLAS UK s growth in supplying UK and global markets with submarine and ship systems. This includes sonar, autonomous systems, marine electric actuation and mine counter-measures. Our Portland Harbour waterside facilities provide an excellent environment to test systems at sea. As a leading innovative maritime systems company, TKMS ATLAS UK operate throughout all phases of the acquisition and engineering lifecycles, from concept to In-service Support. • Competitive salary • Career Development and Training • 25 days holiday (increasing to 28 days after 5 years employment and 30 days after 10 years) • Dental Cover and Employee Assistance Programme • Flexible working patterns At TKMS ATLAS UK, we support our staff to create work-life balance and encourage applications from individuals who are looking for part time or condensed hours as well as full time opportunities. The successful candidate must be able to achieve full SC (Security Clearance).
Senior Quality Specialist Location: Coventry, West Midlands, CV3 2RQ Salary: Competitive, DOE Contract: Permanent, Full time Benefits: • Competitive salary • Contributory pension scheme • Life cover • Incapacity benefits • Cash Back Medical Scheme About the Company: We are an innovative medical devices manufacturer of advanced wound care products, including combination products, from gelling fibres and fabrics. We deliver innovative, cost effective and quality products and solutions for the advanced wound care industry helping to improve patient care and wellbeing. About the Role: Currently an exciting opportunity has arisen for a motivated and dynamic Senior Quality Specialist to join and support Quality Assurance team. The role is responsible for supporting the management and continued effectiveness of Quality Management System within the business. The Senior Specialist will work closely with the Quality Manager to develop and deliver a range of proactive and responsive QMS and Supplier Quality Assurance (SQA) initiatives. Senior Quality Specialist - Duties to include: • Lead supplier management including qualifications, performance evaluations, audits, complaints, and corrective actions (SCARs), • Lead the management of the business product and process change control programme, • Lead the maintenance and management of the SFM standards database, ensuring all standards are current, • Lead the asset calibration programme, • Support the management of the SFM training programme, ensuring training matrices and records are maintained, • Support the management and co-ordination document control within the business via use of the electronic document control system, contributing to the drafting of documentation, managing the review, approval and distribution of documents including procedures, SOPs, WIs, and forms within the SFM QMS, • Support the management and maintenance of the businesses integrated quality management system, • Support the delivery and management of the business nonconformity programme, • Support the delivery of the business audit programme including internal, customer, external, and supplier audits, • Deputise for the Quality Manager as required, • Contribute to create and maintain a proactive leadership style and compliance culture throughout the company to achieve high standards of excellence, sharing best practice, Senior Quality Specialist - Key skills / abilities: • Regulatory, science or engineering degree or equivalent • Knowledge of the Medical Device Directive 93/42/EEC, Regulation EU 2017/745/EEC, USA 21 CFR 820, UKCA • A demonstrable working knowledge and experience of applying ISO 13485, USA 21 CFR 820, EU MDR 2017/745, and Canada SOR 98.282 requirements within the Medical Devices or Pharmaceutical industries • Dynamic and pragmatic team member and flexibility to work within the dynamics of a cross-functional team • Strong communication skills Desirable Additional Experience: • ISO 13485 auditor qualification desirable • Advanced wound care manufacturing an advantage • Cleanroom experience an advantage Important Information: Due to the number of applications we receive, we will only contact those candidates that we want to take forward to interview; if you do not hear from us within 4 weeks, please assume that your application has been unsuccessful on this occasion. If you have the skills and experience we require for this role and are looking for a new challenge, please click on APPLY Today and forward an up-to-date CV and cover letter, explaining why you are a good fit for this role. No Agencies please!
Oct 06, 2025
Full time
Senior Quality Specialist Location: Coventry, West Midlands, CV3 2RQ Salary: Competitive, DOE Contract: Permanent, Full time Benefits: • Competitive salary • Contributory pension scheme • Life cover • Incapacity benefits • Cash Back Medical Scheme About the Company: We are an innovative medical devices manufacturer of advanced wound care products, including combination products, from gelling fibres and fabrics. We deliver innovative, cost effective and quality products and solutions for the advanced wound care industry helping to improve patient care and wellbeing. About the Role: Currently an exciting opportunity has arisen for a motivated and dynamic Senior Quality Specialist to join and support Quality Assurance team. The role is responsible for supporting the management and continued effectiveness of Quality Management System within the business. The Senior Specialist will work closely with the Quality Manager to develop and deliver a range of proactive and responsive QMS and Supplier Quality Assurance (SQA) initiatives. Senior Quality Specialist - Duties to include: • Lead supplier management including qualifications, performance evaluations, audits, complaints, and corrective actions (SCARs), • Lead the management of the business product and process change control programme, • Lead the maintenance and management of the SFM standards database, ensuring all standards are current, • Lead the asset calibration programme, • Support the management of the SFM training programme, ensuring training matrices and records are maintained, • Support the management and co-ordination document control within the business via use of the electronic document control system, contributing to the drafting of documentation, managing the review, approval and distribution of documents including procedures, SOPs, WIs, and forms within the SFM QMS, • Support the management and maintenance of the businesses integrated quality management system, • Support the delivery and management of the business nonconformity programme, • Support the delivery of the business audit programme including internal, customer, external, and supplier audits, • Deputise for the Quality Manager as required, • Contribute to create and maintain a proactive leadership style and compliance culture throughout the company to achieve high standards of excellence, sharing best practice, Senior Quality Specialist - Key skills / abilities: • Regulatory, science or engineering degree or equivalent • Knowledge of the Medical Device Directive 93/42/EEC, Regulation EU 2017/745/EEC, USA 21 CFR 820, UKCA • A demonstrable working knowledge and experience of applying ISO 13485, USA 21 CFR 820, EU MDR 2017/745, and Canada SOR 98.282 requirements within the Medical Devices or Pharmaceutical industries • Dynamic and pragmatic team member and flexibility to work within the dynamics of a cross-functional team • Strong communication skills Desirable Additional Experience: • ISO 13485 auditor qualification desirable • Advanced wound care manufacturing an advantage • Cleanroom experience an advantage Important Information: Due to the number of applications we receive, we will only contact those candidates that we want to take forward to interview; if you do not hear from us within 4 weeks, please assume that your application has been unsuccessful on this occasion. If you have the skills and experience we require for this role and are looking for a new challenge, please click on APPLY Today and forward an up-to-date CV and cover letter, explaining why you are a good fit for this role. No Agencies please!
Compliance Consultant - 12 months contract - Hybrid (London) (Compliance consultant, Internal Controls Consultant, QA Assessor, Quality Control Consultant, QA Assurance, ISO9001 Auditor, ISO9002 Auditor, Quality Assurance Auditor, Quality Assurance Assessor, QA Auditor, Compliance auditor, cards, payments, card scheme, compliance assessor, SOP, SOPs, Job Aid, Job Aid, Complaint, Complaints, Salesforce, Quality Auditor) My client has in the last 18 months set up a new team within their organisation the area of payments acceptance. The team needs a new person to come in and ensure that the teams is covering and adhering to all team areas of compliance with respect to Standard Operating Procedures (SOPs) and Job Aids. This person will do sample internal audits, ensure all procedures are adhered to, everyone on the team is trained and aware of the policies to insure internal and legal and regulatory compliance and company policies and procedures Candidate should be familiar with sales force as user. As the company operates in financial services specifically card scheme payments, experience of this area is preferred. Full spec is available below Compliance & Process Control Specialist About the Role We are seeking a detail-oriented Compliance & Process Control Specialist to ensure that our team operates in line with company policies, industry regulations, and best practices. This role is critical in safeguarding our compliance culture, reviewing and enhancing controls, and fostering collaboration between management and staff to ensure procedures are clear, effective, and consistently followed. Key Responsibilities Monitor team adherence to company compliance rules, policies, and regulatory requirements. Review and maintain Standard Operating Procedures (SOPs), job aids, and process documents in collaboration with managers and internal stakeholders. Design, implement, and regularly review operational controls to ensure compliance. Conduct internal checks, dummy audits, and case reviews to validate adherence to procedures. Oversee the staff training compliance program: track completion, follow up with managers, and ensure mandatory trainings are up to date. Support the complaints-handling process, ensuring alignment with regulatory standards in the financial and regulated environment. Facilitate communication across teams to reinforce compliance awareness and expectations. Work closely with management and internal representatives (eg, compliance, risk, legal teams) to ensure SOPs and job aids meet regulatory and company guidelines. Drive continuous improvements by updating SOPs and processes on a regular basis. Act as a compliance ambassador within the team, fostering a culture of accountability and integrity. Qualifications & Skills Proven experience in compliance, audit, risk management, or process control (preferably in a financial services or regulated environment). Strong knowledge of compliance frameworks, complaints handling processes, and regulatory standards. Excellent attention to detail with strong analytical and critical thinking skills. Experience creating, reviewing, and maintaining SOPs, job aids, and internal controls. Strong interpersonal and communication skills to engage with management, staff, and regulatory partners. Ability to conduct audits or case reviews with accuracy and objectivity. Proactive, organized, and capable of managing multiple priorities. Preferred Experience Familiarity with Salesforce as a tool for case management, reporting, and compliance tracking. Experience with regulatory bodies and compliance standards in the financial industry. Prior role in compliance operations, internal audit, or quality assurance. What We Offer Hybrid flexible working options An opportunity to play a key role in maintaining compliance excellence. A collaborative environment where your input directly impacts operational integrity. Location: London/Hybrid. The company formal policy is currently 2 days a week on site, rest remote. Though this team are flexible so could be 1 day on site one month, 6 days the next month. Please send CV in first instance to be considered
Oct 06, 2025
Contractor
Compliance Consultant - 12 months contract - Hybrid (London) (Compliance consultant, Internal Controls Consultant, QA Assessor, Quality Control Consultant, QA Assurance, ISO9001 Auditor, ISO9002 Auditor, Quality Assurance Auditor, Quality Assurance Assessor, QA Auditor, Compliance auditor, cards, payments, card scheme, compliance assessor, SOP, SOPs, Job Aid, Job Aid, Complaint, Complaints, Salesforce, Quality Auditor) My client has in the last 18 months set up a new team within their organisation the area of payments acceptance. The team needs a new person to come in and ensure that the teams is covering and adhering to all team areas of compliance with respect to Standard Operating Procedures (SOPs) and Job Aids. This person will do sample internal audits, ensure all procedures are adhered to, everyone on the team is trained and aware of the policies to insure internal and legal and regulatory compliance and company policies and procedures Candidate should be familiar with sales force as user. As the company operates in financial services specifically card scheme payments, experience of this area is preferred. Full spec is available below Compliance & Process Control Specialist About the Role We are seeking a detail-oriented Compliance & Process Control Specialist to ensure that our team operates in line with company policies, industry regulations, and best practices. This role is critical in safeguarding our compliance culture, reviewing and enhancing controls, and fostering collaboration between management and staff to ensure procedures are clear, effective, and consistently followed. Key Responsibilities Monitor team adherence to company compliance rules, policies, and regulatory requirements. Review and maintain Standard Operating Procedures (SOPs), job aids, and process documents in collaboration with managers and internal stakeholders. Design, implement, and regularly review operational controls to ensure compliance. Conduct internal checks, dummy audits, and case reviews to validate adherence to procedures. Oversee the staff training compliance program: track completion, follow up with managers, and ensure mandatory trainings are up to date. Support the complaints-handling process, ensuring alignment with regulatory standards in the financial and regulated environment. Facilitate communication across teams to reinforce compliance awareness and expectations. Work closely with management and internal representatives (eg, compliance, risk, legal teams) to ensure SOPs and job aids meet regulatory and company guidelines. Drive continuous improvements by updating SOPs and processes on a regular basis. Act as a compliance ambassador within the team, fostering a culture of accountability and integrity. Qualifications & Skills Proven experience in compliance, audit, risk management, or process control (preferably in a financial services or regulated environment). Strong knowledge of compliance frameworks, complaints handling processes, and regulatory standards. Excellent attention to detail with strong analytical and critical thinking skills. Experience creating, reviewing, and maintaining SOPs, job aids, and internal controls. Strong interpersonal and communication skills to engage with management, staff, and regulatory partners. Ability to conduct audits or case reviews with accuracy and objectivity. Proactive, organized, and capable of managing multiple priorities. Preferred Experience Familiarity with Salesforce as a tool for case management, reporting, and compliance tracking. Experience with regulatory bodies and compliance standards in the financial industry. Prior role in compliance operations, internal audit, or quality assurance. What We Offer Hybrid flexible working options An opportunity to play a key role in maintaining compliance excellence. A collaborative environment where your input directly impacts operational integrity. Location: London/Hybrid. The company formal policy is currently 2 days a week on site, rest remote. Though this team are flexible so could be 1 day on site one month, 6 days the next month. Please send CV in first instance to be considered
Job Title: QA Location: Bedfordshire Salary: 29,000 - 31,000 Ref: AM20448 Are you passionate about food quality and wanting a new opportunity? Want to have your weekends free and work Monday to Friday? Keen to join a company that is growing? If so, we want to hear from you! We are working with an award-winning food business, that supplies premium product to many of the retailers. They are looking for passionate Quality Auditor to come and join the team. As Quality Auditor you will work closely with all teams to ensure that all product is produced as per customer specifications. Complete quality records daily or against the agreed frequency detailed in the product specification. Daily completion of quality start up and completion checks. Daily production quality checks such as torque tests and product weight checks, paperwork checks, ensuring all batch codes and dates are entered and correct. This will suit a food manufacturing QA who can make decisions on quality, has good knowledge of HACCP and sampling practices, excellent communication at all levels and able to manage and work effectively within a busy team. Good IT skills are essential and full driving licence are also needed. If this sounds like you, please apply via the link. Alternatively, for a confidential chat about the role, please contact Alex on (phone number removed) or (url removed).
Oct 05, 2025
Full time
Job Title: QA Location: Bedfordshire Salary: 29,000 - 31,000 Ref: AM20448 Are you passionate about food quality and wanting a new opportunity? Want to have your weekends free and work Monday to Friday? Keen to join a company that is growing? If so, we want to hear from you! We are working with an award-winning food business, that supplies premium product to many of the retailers. They are looking for passionate Quality Auditor to come and join the team. As Quality Auditor you will work closely with all teams to ensure that all product is produced as per customer specifications. Complete quality records daily or against the agreed frequency detailed in the product specification. Daily completion of quality start up and completion checks. Daily production quality checks such as torque tests and product weight checks, paperwork checks, ensuring all batch codes and dates are entered and correct. This will suit a food manufacturing QA who can make decisions on quality, has good knowledge of HACCP and sampling practices, excellent communication at all levels and able to manage and work effectively within a busy team. Good IT skills are essential and full driving licence are also needed. If this sounds like you, please apply via the link. Alternatively, for a confidential chat about the role, please contact Alex on (phone number removed) or (url removed).
Westlakes Recruit are currently recruiting for an experienced Quality Inspector be engaged on a contract basis in Bristol/Bridgwater. Role Description: Conduct on-site field inspection activities Carrying out measurement activities to ensure that they meet the required specifications and are compliant. Liaise with all relevant stakeholders including the Team, Client and Supply chain to ensure QC guidance is provided and adhered to. Ensure compliance, investigation of non-conforming products/processes and ensuring effective corrective and preventive action is taken to close out NCRs. Facilitate and support project team with root cause analysis, corrective action, and continual improvement of processes. Management and assurance of Life-Time Quality Records generated in support of activities performed on a highly regulated nuclear site. Provide Review, approval, management and verification of supplier Manufacturing Inspection and Test Plans required for activities performed on and off site. Ensure the quality of the project, product, records, service and their supporting processes meet the standards and specifications required by the associated NEC4 contract. Duties: Carry out project QC activities in accordance with client contract requirements. Root cause analysis and implementation of corrective action for process related concerns. Assist in establishing, implementing and maintaining the quality management system. Work in line with the management system and support any improvement opportunities in process and work instructions. Escalate all issues to the Quality Engineers and Managers. Carry out internal audit and supplier audit as requested by internal stakeholders, ensuring contract quality requirements are in accordance with client specifications. Provide support to staff to ensure that processes comply with the relevant requirements of the contract specification, quality plans, the quality management system and international standards Conduct audits, including closing out audit findings, creating audit finding reports and determine proper corrective and preventive actions. Ensuring that the arrangements identified in the Project QA/QC Strategy are implemented within the project; typically this will include the Project Execution Populating the supplier Quality Plans and Inspection and Test plans with the appropriate hold witness and review points. Carrying out monitoring, witness inspections, test and verifications as identified in the supplier Quality or Inspection and Test Plan. Ensure that Lifetime Quality Records are being generated and verified concurrent with manufacturing, installation or build activities. Raising non-conformance report for products / services that do not satisfy the specified requirements. Promote company and client quality objectives and expectations. Qualifications / Experience Civils/Mech/EC&I background required ISO 9001 Lead Auditor / Internal Auditor. QC grade Training desirable Third party / supplier auditing. NCR generation and management. Working knowledge of ISO 9001:2015 Understanding of ISO 14001 / 45001 requirements. Worked in highly regulated industries. Experience and understanding of process improvement. Membership of appropriate professional body (I.e., CQI) or willingness to attain. Experience of working in highly regulated industry. Min requirements Proven and Solid experience in area of specialisation. QC Grade Training advantageous. Auditor/lead auditor certificate desired. Good oral and written communication skills; working knowledge of word-processing and integrated software applications; organisational skills and ability to perform detail-oriented work are required. Position may require travel. Successful candidates to ideally be Security Cleared (SC) or have no issue in obtaining SC. Why We're Different: Westlakes Recruit are a people solutions business that understands the complexities of nuclear and the importance of our clients' mission critical objectives. Smarter, faster, more agile - we have a laser focus on nuclear, with deep sectoral knowledge. We develop nuclear talent pools before you know you need them! We do Nuclear. We only do Nuclear. We do all of Nuclear. Powering a Diverse Nuclear Future: As an equal opportunities business, we value applications from all backgrounds, cultures and abilities.
Oct 03, 2025
Contractor
Westlakes Recruit are currently recruiting for an experienced Quality Inspector be engaged on a contract basis in Bristol/Bridgwater. Role Description: Conduct on-site field inspection activities Carrying out measurement activities to ensure that they meet the required specifications and are compliant. Liaise with all relevant stakeholders including the Team, Client and Supply chain to ensure QC guidance is provided and adhered to. Ensure compliance, investigation of non-conforming products/processes and ensuring effective corrective and preventive action is taken to close out NCRs. Facilitate and support project team with root cause analysis, corrective action, and continual improvement of processes. Management and assurance of Life-Time Quality Records generated in support of activities performed on a highly regulated nuclear site. Provide Review, approval, management and verification of supplier Manufacturing Inspection and Test Plans required for activities performed on and off site. Ensure the quality of the project, product, records, service and their supporting processes meet the standards and specifications required by the associated NEC4 contract. Duties: Carry out project QC activities in accordance with client contract requirements. Root cause analysis and implementation of corrective action for process related concerns. Assist in establishing, implementing and maintaining the quality management system. Work in line with the management system and support any improvement opportunities in process and work instructions. Escalate all issues to the Quality Engineers and Managers. Carry out internal audit and supplier audit as requested by internal stakeholders, ensuring contract quality requirements are in accordance with client specifications. Provide support to staff to ensure that processes comply with the relevant requirements of the contract specification, quality plans, the quality management system and international standards Conduct audits, including closing out audit findings, creating audit finding reports and determine proper corrective and preventive actions. Ensuring that the arrangements identified in the Project QA/QC Strategy are implemented within the project; typically this will include the Project Execution Populating the supplier Quality Plans and Inspection and Test plans with the appropriate hold witness and review points. Carrying out monitoring, witness inspections, test and verifications as identified in the supplier Quality or Inspection and Test Plan. Ensure that Lifetime Quality Records are being generated and verified concurrent with manufacturing, installation or build activities. Raising non-conformance report for products / services that do not satisfy the specified requirements. Promote company and client quality objectives and expectations. Qualifications / Experience Civils/Mech/EC&I background required ISO 9001 Lead Auditor / Internal Auditor. QC grade Training desirable Third party / supplier auditing. NCR generation and management. Working knowledge of ISO 9001:2015 Understanding of ISO 14001 / 45001 requirements. Worked in highly regulated industries. Experience and understanding of process improvement. Membership of appropriate professional body (I.e., CQI) or willingness to attain. Experience of working in highly regulated industry. Min requirements Proven and Solid experience in area of specialisation. QC Grade Training advantageous. Auditor/lead auditor certificate desired. Good oral and written communication skills; working knowledge of word-processing and integrated software applications; organisational skills and ability to perform detail-oriented work are required. Position may require travel. Successful candidates to ideally be Security Cleared (SC) or have no issue in obtaining SC. Why We're Different: Westlakes Recruit are a people solutions business that understands the complexities of nuclear and the importance of our clients' mission critical objectives. Smarter, faster, more agile - we have a laser focus on nuclear, with deep sectoral knowledge. We develop nuclear talent pools before you know you need them! We do Nuclear. We only do Nuclear. We do all of Nuclear. Powering a Diverse Nuclear Future: As an equal opportunities business, we value applications from all backgrounds, cultures and abilities.
Computer Futures - London & S.E(Permanent and Contract)
Stoke-on-trent, Staffordshire
We are seeking a Project Quality Engineer to support the delivery of high-value engineering projects involving piping systems, pressure vessels, and process equipment. The successful candidate will ensure quality compliance across all phases of project execution, from design through to fabrication and installation. Key Responsibilities Develop and implement Project Quality Plans aligned with client and regulatory requirements. Conduct quality audits on suppliers, fabrication yards, and site installations. Review and approve Inspection Test Plans (ITPs), welding procedures, and material certifications. Liaise with engineering, procurement, and construction teams to ensure quality standards are met. Manage non-conformance reports (NCRs) and ensure timely resolution. Support pre-commissioning and final handover documentation. Ensure compliance with ASME, API, PED, and other relevant standards. Essential Experience Proven experience as a Quality Engineer onmulti-disciplinary engineering projects involving: Piping systems Pressure vessels Skid-mounted process units Strong understanding of fabrication and welding processes. Familiarity with QA/QC documentation, traceability, and certification requirements. Experience working with EPC contractors or OEMs in the process, chemical, or energy sectors. Ability to work independently and manage quality across multiple work fronts. Qualifications Degree or HNC/HND in Mechanical Engineering or related discipline. Recognised quality certification (eg, ISO 9001 Lead Auditor, CSWIP, PCN) is desirable. Working knowledge of UK and EU regulations for pressure equipment. Contract Details Rate: £65/hour (Outside IR35) Duration: 6 months Location: Stoke (site-based) Working Arrangement: Site-based with potential flexibility depending on project phase Please visit our website to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement. To find out more about Computer Futures please visit our website Computer Futures, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales
Oct 03, 2025
Contractor
We are seeking a Project Quality Engineer to support the delivery of high-value engineering projects involving piping systems, pressure vessels, and process equipment. The successful candidate will ensure quality compliance across all phases of project execution, from design through to fabrication and installation. Key Responsibilities Develop and implement Project Quality Plans aligned with client and regulatory requirements. Conduct quality audits on suppliers, fabrication yards, and site installations. Review and approve Inspection Test Plans (ITPs), welding procedures, and material certifications. Liaise with engineering, procurement, and construction teams to ensure quality standards are met. Manage non-conformance reports (NCRs) and ensure timely resolution. Support pre-commissioning and final handover documentation. Ensure compliance with ASME, API, PED, and other relevant standards. Essential Experience Proven experience as a Quality Engineer onmulti-disciplinary engineering projects involving: Piping systems Pressure vessels Skid-mounted process units Strong understanding of fabrication and welding processes. Familiarity with QA/QC documentation, traceability, and certification requirements. Experience working with EPC contractors or OEMs in the process, chemical, or energy sectors. Ability to work independently and manage quality across multiple work fronts. Qualifications Degree or HNC/HND in Mechanical Engineering or related discipline. Recognised quality certification (eg, ISO 9001 Lead Auditor, CSWIP, PCN) is desirable. Working knowledge of UK and EU regulations for pressure equipment. Contract Details Rate: £65/hour (Outside IR35) Duration: 6 months Location: Stoke (site-based) Working Arrangement: Site-based with potential flexibility depending on project phase Please visit our website to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement. To find out more about Computer Futures please visit our website Computer Futures, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales
