Get new jobs by email
- ...Freelance ISO Lead Auditor / Consultant UK Remote (with occasional on-site client visits) Contract / Self-Employed Basis About... ...Auditor (or equivalent) certification is a must Experience with ISO 13485:2026 Proven background in implementing and/or auditing...SuggestedSelf-employedFreelanceRemoteFlexible hours
- £44k - £56k per annumEstimated...we cover most verticals). The Partnership Manager will play a critical role in growing the business by identifying and converting new ISO & Referral opportunities and nurturing relationships. Responsibilities Responsible for sourcing, meeting and boarding ISOs & Referral...SuggestedFull-time
£40k - £45k per annum
...ISO and Compliance Manager Location: Ringwood, Hampshire + non-contractual hybrid home working Salary: £40,000 – £45,000 DoE + Profit Share + Benefits Hours: 37.5 hours per week The Role Are you an experienced ISO and Compliance Manager, who ensures an organisation...SuggestedFull-timeHybrid workingWork from home- £46k - £61k per annumEstimatedFreelance Auditor – ISO 9001 / 14001 / 45001 (Oil & Gas) Location: Edinburgh - Aberdeen corridor Engagement: Freelance / Contract Start Date: From late Q2 2026 onwards Rates: Competitive day rates About Bureau Veritas Bureau Veritas is a world...SuggestedDaily payOngoing contractFreelanceOn-siteFlexible hours
- ...About IMSM IMSM (International Management Systems Marketing) is a global force in ISO consultancy - helping organisations not just achieve certification, but transform the way they operate. We partner with businesses across every sector, elevating performance, boosting...SuggestedHybrid workingRemoteFlexible hours
- £45k - £59k per annumEstimated...processes across R&D, Marketing, Finance, Manufacturing, and Regulatory. Track progress, report updates, and ensure compliance with ISO 13485, GMP, and FDA 21 CFR 820. Ensure product quality and successful project delivery. About You Degree in Mechanical...SuggestedFull-time
- £27k - £36k per annumEstimated...• Comprehensive knowledge particularly of FDA, EU IVDR and MDSAP countries. • Strong understanding of quality management systems (ISO 13485, GMP, MDSAP) • Experience preparing and reviewing technical documentation and regulatory submissions • Sound understanding in product...SuggestedRemote jobOn-siteMonday to Friday
- £35k - £47k per annumEstimated...adjustments to resolve any issues. Ensure that electromechanical compositions align with applicable regulatory standards (e.g., FDA, ISO 13485). Supplier Coordination: Coordinate supplier changes, including assessing the impact of changes on electromechanical systems....SuggestedRemote jobFull-timeOn-siteMonday to Friday
- £70k - £88k per annumEstimated...IT skills, problem solving ability, analytical and communication skills. Knowledge, Skills and Abilities: Understanding of ISO 13485 requirements and EU medical device regulations. Ability to read and understand technical material. Excellent attention to...Suggested40 hours/weekFlexible hours
- £39k - £51k per annumEstimated...discipline with knowledge of mechanical / design engineering. ~ Experience in an R&D medical devices environment. ~ Understanding of the ISO 13485 and 14971 standards, and FDA regulations for design controls. ~ Ability to use CAD software packages (SolidWorks). ~...SuggestedHybrid workingRelocationFlexible hoursNight shift
- £41k - £53k per annumEstimated...to enhance delivery performance and cost optimisation. · Ensuring all material planning activities comply with relevant standards (ISO 13485, FDA, BSI). · Continuously assess and optimise planning processes to drive efficiency, scalability, and cost-effectiveness. Implement...Suggested
£53k per annum
.... Key Responsibilities: Develop and maintain project plans, schedules and budgets. Ensure compliance with QMS requirements (ISO 13485, ISO 9001, ISO 14971). Communicate clearly with engineering, design and client teams. Identify risks and support mitigation strategies...SuggestedFull-timeSummer workHybrid workingFlexible hours- £52k - £66k per annumEstimated...engagements, including: Quality assurance and compliance Working within and advising on Quality Management Systems compliant with ISO 13485, QMSR, 21 CFR Part 4 and relevant GxP requirements. Authoring, reviewing and maintaining Design History Files, risk management...SuggestedFull-timeHybrid workingOn-site5 days/week
£2,500 per month
...apprenticeship in Mechanical Engineering Experience within non-woven, conversion or medical device manufacturing Familiarity with ISO 13485 Personal attributes: Hands-on and proactive Strong communication and influencing skills Well organised with good planning...SuggestedFull-timeApprenticeship£25.76k - £27.48k per annum
...standard of work required. Support the Team Leader by ensuring that all staff carry out their duties in accordance with the departments ISO 13485:2016 Quality Policies and Procedures. Monitor and investigates complaints and concerns and ensure faults are rectified and aid in...SuggestedFull-timeShift work- £23k - £30k per annumEstimated...expected to have extensive knowledge and skills of all Departmental quality documents and SOPs used to control the production in an ISO 13485-certified department and, as such, will be responsible for ensuring staff conform to the Sterile Services and Endoscopy Decontamination...Full-timeImmediate start
£66.58k - £77.37k per annum
...compliance with Department of Health, MHRA, Care Quality Commission, ISO and HTM requirements for decontamination. Develop, implement and... ...requirements for clinical users. Maintain compliance with ISO 13485, ISO 9001, MHRA regulations, and other external accreditation/audit...Full-time£45k - £57k per annum
...contribute to continuous improvement of engineering processes and ways of working Tools and standards exposure may include: ISO 13485, IEC 60601, or similar regulated frameworks Medical device, health tech, or high‑reliability product environments About You:...Full-time£38k per annum
...manufacturing environment • Hands-on experience with inspections, non-conformance, and product release • Working knowledge with ISO standards (13485, 9001, 14001) and/or FDA requirements • High attention to detail with confidence to challenge and escalate issues •...Monday to Friday£28k - £30k per annum
...skills and experience Knowledge of and practical experience of ISO 22716, REACh, Schedule 34 of The Product Safety and Metrology etc.... ...working environment Experience of working to standards ISO 9001, 13485, FDA Certified Internal Quality Auditor to ISO9001 standard....Long-term contractPermanentFull-timeMonday to ThursdayFlexible hours- ...Oversight (Core Responsibility) ● Own preparation, maintenance, and update of software validation plans in line with IEC 62304, ISO 13485, and internal QMS requirements. ● Ensure validation scope aligns with intended use, risk classification, and release strategy....Long-term contractHybrid workingOn-siteRemoteFlexible hours
- £43k - £57k per annumEstimated...Safety with a desire to progress within this field Technical Skills and Experience Desired Working within an ISO 9001 Quality Assurance system & ISO 13485 - Quality Management for Medical Devices Positive and optimistic within a fast growing organisation. Strong...Full-time
- £31k - £41k per annumEstimated...and procedures. Ensure that the Quality Management system in place conforms with all relevant Quality standards which include ISO 9001, ISO 13485 and ISO 22716 Manage and update the site Quality Manual and conduct Training Ensure the legal compliance of New Products...Permanent
- £36k - £48k per annumEstimated...design performance Create and review specifications of refrigeration systems and components Meet regulatory compliance to ISO 9001, ISO 13485 and organisation requirements Guide testing engineers on testing planning and execution Feed the refrigeration technology...Permanent
- £37k - £49k per annumEstimated...travel at short notice where required to meet urgent service needs. Maintain accurate service records, reports, and logs in line with ISO 13485:2016 QMS procedures. Ensure compliance with all health, safety, and regulatory standards. Assist with logistics including...
- £65k - £83k per annumEstimated...Pharmaceutical Industries or equivalent. A proven track record in managing medical device design and development projects, working within ISO 13485, EN 60601, and risk management processes of ISO 14971. Excellent communication and presentation skills, commercially astute with...Full-timeOn-siteRemote
- £40k - £53k per annumEstimated...Quality Engineering, Supplier Quality, or Supplier Management within a regulated manufacturing environment. Experience working within ISO 13485 environments required; experience with 21 CFR Part 820 or GMP-regulated industries preferred. Knowledge, Skills, and Abilities...PermanentFull-time
£50k - £60k per annum
...metrics and contribute to new product introduction (NPI) activities. Knowledge, Skills & Experience: Strong knowledge of ISO 9001, ISO 13485, and quality management systems. Proven experience in manufacturing quality and process improvement. Skilled in data analysis...PermanentFull-timeMonday to Friday£49.39k - £56.52k per annum
...information and track-and-trace systems. Quality management, compliance & audit Support the operation of the Quality Management System (ISO 13485), including SOPs, records, and all controlled documents. Ensure compliance with HTM 0101, MHRA requirements, and internal governance...Full-time£40k - £48k per annum
...customers and internal teams. • Strong organisational and time management skills. • Experience working within ISO 9001 quality management systems (ISO 13485 knowledge would be advantageous). Salary & Benefits: • £40,000 – £48,000 salary • 37.5 hour week...Full-timeMonday to Thursday

