Regulatory Medical Device jobs in London
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- Experience with Class III medical device validation and regulatory compliance frameworks.
- Scope to develop deeper expertise in medical device validation and…
- Experience with Class III medical device validation and regulatory compliance frameworks.
- Scope to develop deeper expertise in medical device validation and…
- Experience with Class III medical device validation and regulatory compliance frameworks.
- Scope to develop deeper expertise in medical device validation and…
View similar jobs with this employerSThreeIlford- Work from home
- Advanced certifications in quality assurance or medical device compliance.
- Executing system validation testing across Class III medical device development.
- AWS EMEA SARL (UK Branch)London
- Understanding of the regulatory landscape for these sectors including AI-enabled medical devices and clinical decision support tools.
- A day in the life.
- Medpace, Inc.London EC4V 3BJ
- Annual leave
- Company events
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Senior/Managing Consultant: Chemical Regulatory
Often replies in 1 dayYordas GroupUnited Kingdom- Company pension
- Co-ordinate, lead and develop the team of internationally based regulatory consultants engaged in global notification services (ca. 10 - 15 staff).
Associate Biostatistical Director
Often replies in 1 dayNEXUSCW LTDLondon EC3V 9DU- Molecular diagnostics, IVD/medical device, or pharmaceutical industry experience strongly preferred.
- Demonstrated success leading the statistical components of…
- Jazz PharmaceuticalsLondon W1G
- Annual leave
- Leads the medical safety contributions of global regulatory submissions for new products, formulations or indications.
- NTT Global Data CentersHemel Hempstead
- Annual leave
- A monthly stipend is provided to cover expenses associated with working remotely and use of a personal mobile device.
- Jazz PharmaceuticalsLondon W1G
- Annual leave
- Keeps abreast of new PV/safety regulations and guidance from the regulatory authorities.
- Perform review of medical/scientific literature to identify literature…
View similar jobs with this employerSThreeLondon- Work from home
- Advanced certifications in quality assurance or medical device compliance.
- Executing system validation testing across Class III medical device development.
View similar jobs with this employerJazz PharmaceuticalsLondon W1T- Annual leave
- Ensuring compliance with regulatory requirements and data privacy standards.
- Experience with natural language processing and generative AI for medical text…
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- Development/authorship of CMC regulatory filings for pharmaceutical products.
- Author CMC sections of regulatory dossiers for products at all stages to enable…
- NTT Global Data CentersHemel Hempstead
- Referral programme
- Annual leave
- Support compliance with applicable legal, regulatory, and corporate governance requirements.
- A monthly stipend is provided to cover expenses associated with…
- RELXFarringdon
- Flexible schedule
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Job Post Details
System Validation Engineer - job post
3.33.3 out of 5 stars
London
£250 - £400 a day - Part-time
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Job details
Pay
- £250 - £400 a day
Job type
- Part-time
Location
London
Full job description
Please note the content of this advert does not represent a live vacancy.About the opportunityThis is an opportunity to register your interest in future System Validation Engineer roles within medical device development, positions that could support the delivery of safe, compliant Class III medical devices to patients.Roles of this type may sit within a quality-focused engineering environment where validation and regulatory compliance are central to success. The work could involve collaborating across product development, quality assurance and regulatory teams to ensure that systems meet rigorous international standards including ISO 13485 and IEC 62304, with scope to contribute to the validation strategy for sophisticated medical devices.Typical role overview
- Location: UK-wide (nationwide)
- Type: Contract · Full-time
- Day Rate: £300–400 per day (or £250–280 per day dependent on experience and contract terms)
- Qualification: Bachelor's degree in Computer Science or related discipline
- Domain: Class III Medical Device · ISO 13485 · IEC 62304
- Developing and executing comprehensive validation protocols and test plans for medical device systems
- Conducting system-level validation testing to demonstrate compliance with ISO 13485 and IEC 62304 requirements
- Collaborating with product engineering, quality and regulatory teams to define validation scope and acceptance criteria
- Documenting validation activities, results and traceability to design specifications and regulatory requirements
- Supporting the preparation and maintenance of validation reports for regulatory submissions
- Contributing to the continuous improvement of validation methodologies and processes
- Troubleshooting validation failures and supporting root cause analysis and corrective action
- Bachelor's degree in Computer Science, Engineering, or a related technical discipline
- Demonstrated experience in system validation or quality assurance for regulated medical device environments
- Working knowledge of ISO 13485 (Medical Device Quality Management) and IEC 62304 (Software Lifecycle Processes)
- Experience with Class III medical device validation and regulatory compliance frameworks
- Strong technical documentation and report writing skills
- Familiarity with validation tools, test management systems and traceability matrices
- Ability to work independently and collaboratively across cross-functional teams
- Excellent attention to detail and commitment to regulatory compliance
- The opportunity to contribute to the safe delivery of life-changing Class III medical devices
- Experience working within a highly regulated, quality-focused environment
- Scope to develop deeper expertise in medical device validation and regulatory frameworks
- Potential progression toward more senior validation and quality leadership roles
- Exposure to cutting-edge medical device technologies and therapeutic areas
- Professional development within a collaborative engineering culture
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