Medical Device Engineer jobs in England
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- Computer FuturesLondon
- Ensure compliance with relevant medical device standards and regulatory requirements.
- Knowledge of standards such as ISO 14971, IEC 62304, and related medical…
View similar jobs with this employerSThreeLondon- Experience in regulated industries or ISO 13485 (medical device) environments.
- Design Engineers play a critical role in translating concepts into manufacturable…
View similar jobs with this employerSThreeLondon- This role could sit within a dynamic engineering team focused on product design and development.
- You could work on projects where technical precision, creative…
- Laing O'RourkeDagenham
- Select appropriate BMS controllers, EPMS devices, EMS platforms and field equipment.
- The BEMS Project Design Engineer is responsible for producing high-quality…
- View all Laing O'Rourke jobs - Dagenham jobs - Design Engineer jobs in Dagenham
- Salary Search: BEMS Design Engineer salaries in Dagenham
- See popular questions & answers about Laing O'Rourke
View similar jobs with this employerPA ConsultingMelbourn- Significant experience in medical device and/or drug-device combination product development;
- This role calls for a senior engineer with substantial experience…
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- Power Engineering Consultants PlcAlderley Edge SK9 7JT
- Sick pay
- Relocation assistance
- Free parking
- Company pension
- Private medical insurance
- On-site parking
- Commissioning and Testing: Lead the commissioning process of electrical protection systems, including relays, switchgear, generators, transformers, and other…
- Domain: Class III medical device · validation and compliance.
- Demonstrated experience with ISO 13485 and IEC 62304 in a medical device or comparable regulated…
- ALQUEST Technical RecruitmentCambridge
- Electro mechanical device manufacture and production: 2 years (preferred).
- Collaborate with production line ATE engineers to deliver and deploy testers in…
- Smartbox Assistive TechnologyBristol BS1
- Medical device or safety-critical product development.
- You'll mentor engineers, contribute to technical strategy and support a culture of continuous improvement…
- Johnson MattheyRoyston
- Discounted gym membership
- Working within the Engineering support Team and reporting to the Controls System Lead Engineer, the Software/Controls Engineer (SCE) is responsible for…
- Johnson MattheyRoyston
- Discounted gym membership
- Working within the Engineering support Team and reporting to the Controls System Lead Engineer, the Software/Controls Engineer (SCE) is responsible for…
View similar jobs with this employerSThreeManchester- Professional development in regulated medical device environments.
- Domain: Class III medical device · validation and regulatory compliance.
- Domain: Class III medical device · Validation and quality assurance.
- Involvement in validating medical device systems that support patient safety and clinical…
- Strain Measurement Devices LtdBury St. Edmunds IP29 4UQ
- Company pension
- On-site parking
- Experience in a regulated or high-tech manufacturing environment, preferably involving sensors, electronics, medical devices, semiconductors, thin-film…
- SThreeCambridge
- Prior experience supporting medical device submissions or regulatory inspections.
- Understanding of Class III medical device regulatory requirements and product…
View similar jobs with this employerSThreeManchester- System Validation Engineer opportunities in medical device development typically sit within quality-focused teams delivering Class III medical devices under ISO…
Medical Software Safety Engineer
Job details
Pay
£75,000 a year
Job type
Permanent
Full job description
We're partnering with an innovative medical technology consultancy looking for a Software Safety Engineer to support high-quality software-based medical devices. Key Responsibilities
- Drive software safety activities throughout the product lifecycle.
- Conduct hazard analysis, risk assessments, and safety documentation.
- Collaborate with cross-functional teams including Software, Quality, Regulatory, and Product Development.
- Ensure compliance with relevant medical device standards and regulatory requirements.
- Support verification, validation, and software risk management activities.
- 4 years of experience within the medical device and/or Software as a Medical Device (SaMD) sector.
- Strong understanding of software risk management and functional safety principles.
- Knowledge of standards such as ISO 14971, IEC 62304, and related medical device regulations.
- Up to £85,000
- Share option scheme
- Potential hybrid flexibility
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