Medical Device Company jobs in Cambridge
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- SThreeCambridge
- Understanding of software validation and cybersecurity requirements in medical devices.
- Experience supporting Class III medical device submissions or…
- SThreeCambridge
- Potential to develop specialist expertise in medical device regulations.
- Ensuring product compliance with ISO 13485, IEC 62304 and relevant medical device…
- Everest Clinical ResearchUnited Kingdom
- Work from home
- The acquisition of August Research establishes a European footprint for Everest to provide full-service offerings to its pharmaceutical, biotechnology and…
View similar jobs with this employerMedical Device Regulatory and Quality Consultant
Often replies in 1 dayPA ConsultingMelbourn SG8 6DP- Annual leave
- Company pension
- Private medical insurance
- Cycle to work scheme
- This role focuses on advising clients on the regulatory, Quality and compliance aspects of medical devices, through a strong understanding of regulatory and…
- View all PA Consulting jobs - Melbourn jobs - Medical Consultant jobs in Melbourn
- Salary Search: Medical Device Regulatory and Quality Consultant salaries
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View similar jobs with this employerHoya Vision CareCambridge- Managing and developing a designated sales region.
- Building strong, long-term relationships with optical practices and key stakeholders.
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- Salary Search: Business Development Manager salaries in Cambridge
View similar jobs with this employerHologicCambridge CB4 0WN- Company pension
- Experience in a regulated industry, preferably within medical devices or healthcare technology.
- Lead complaint investigations and perform root cause analysis to…
Clinical Nurse Advisor
Urgently neededWallace Hind SelectionCambridge- Company car
- Company pension
- Private medical insurance
- Pension (up to 8% and matched by company).
- This is a field-based role, delivering clinical customer and device support.
- As our Clinical Nurse Advisor, you will:
- Huxley Bertram Engineering LtdCambridge CB25 9QP
- Annual leave
- Life insurance
- Company pension
- Cycle to work scheme
- On-site parking
- Health & wellbeing programme
- Huxley Bertram Engineering Limited designs and builds bespoke machinery and automated equipment for clients operating in high technology and regulated sectors,…
Production & Test Operative
Often replies in 6 daysStrain Measurement Devices LtdBury St. Edmunds IP29 4UQ- Free parking
- Company pension
- Company events
- On-site parking
- Production Operative – Assembly & Final Test.
- Hours: Full-Time - 39 hours per week (Mon – Thu 07:00-15:45 Fri 07:00-12:00).
- Optimum MedicalUnited Kingdom
- Referral programme
- Annual leave
- Employee discount
- Employee assistance programme
- Free fitness classes
- Company pension
- Experience in continence, urology, or medical devices.
- Strong experience in field-based healthcare or medical sales (NHS-focused).
- Optimum MedicalUnited Kingdom
- Referral programme
- Annual leave
- Employee discount
- Employee assistance programme
- Free fitness classes
- Company pension
- Experience in continence, urology, or medical devices.
- Strong experience in field-based healthcare or medical sales (NHS-focused).
Sales Specialist (Neurodiagnostics) South
Often replies in 3 daysMedevolve LtdUnited Kingdom- Company car
- Private dental insurance
- Company pension
- Private medical insurance
- Car scheme
- You'll be responsible for developing relationships with neurophysiology, vascular, medical physics, sleep and respiratory and procurement departments.
- ClinisuppliesEngland
- Training the clinical staff on the best practices for safe discharge with Nightingale whilst managing a medical device.
- Pay: £32,000.00 per year.
- SThreeCambridge
- Managing regulatory submissions and dossier preparation for medical devices or pharmaceuticals.
- In-depth knowledge of ISO 13485, IEC 62304 and Class III medical…
- KPI Recruiting LtdWaterbeach CB25 9TN
- Financial planning services
- Annual leave
- Company pension
- Private medical insurance
- Car scheme
- Experience within advanced manufacturing, electronics, medical devices, scientific instrumentation, industrial technology, aerospace or similar engineering…
Field Service Technician
Often replies in 6 daysAir Spectrum Environmental LtdUnited Kingdom- Employee discount
- Sick pay
- Bereavement leave
- Company pension
- Private medical insurance
- Company events
- The role mainly consists of visiting customer sites around the UK to service and maintain equipment and install new equipment.
- Must be comutable to Worcester.
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Job Post Details
Regulatory Affairs Specialist - job post
3.33.3 out of 5 stars
Cambridge
£250 - £750 a day - Permanent
You must create an Indeed account before continuing to the company website to apply
Job details
Pay
- £250 - £750 a day
Job type
- Permanent
Location
Cambridge
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 Regulatory Affairs roles, positions that could support organisations in navigating complex regulatory environments and ensuring compliance across their operations. Roles of this type may sit within dynamic, collaborative teams where regulatory expertise directly influences product development, market access and organisational risk management.What you would doTypical responsibilities could include:
- Supporting the development and maintenance of regulatory strategies aligned with product lifecycle and market requirements
- Preparing and submitting regulatory documentation to relevant authorities, including technical files, dossiers and compliance reports
- Monitoring regulatory changes and advising internal teams on implications for current and future products
- Coordinating with cross-functional teams including quality, engineering, clinical and commercial functions
- Maintaining regulatory intelligence and competitor tracking to support strategic planning
- Supporting internal audits and regulatory inspections to ensure ongoing compliance
- Contributing to the interpretation and implementation of regulatory standards such as ISO 13485, IEC 62304 and requirements for Class III medical devices
- Liaising with notified bodies, competent authorities and regulatory consultants as needed
- Bachelor's degree in Business, Life Sciences, Engineering or related discipline
- 3-5 years' experience in regulatory affairs, quality assurance or compliance within a regulated environment
- Demonstrable knowledge of ISO 13485 (Medical Device Quality Management Systems) and IEC 62304 (Medical Device Software Lifecycle Processes)
- Experience supporting Class III medical device submissions or equivalently complex regulatory pathways
- Strong written and verbal communication skills, with the ability to translate complex regulatory requirements for diverse audiences
- Proficiency in interpreting regulatory guidance documents and building compliant documentation
- Organised approach to managing multiple regulatory projects and deadlines
- UK-based or willing to work across UK locations on a nationwide basis
- Certified Compliance Professional (CCP) certification or equivalent
- Experience with regulatory information management systems
- Knowledge of post-market surveillance and adverse event reporting
- Understanding of software validation and cybersecurity requirements in medical devices
- Opportunity to influence product safety, efficacy and market access through rigorous regulatory oversight
- Exposure to the full product lifecycle from development through commercialisation
- Scope to develop deep expertise in regulatory frameworks and emerging compliance requirements
- Potential for progression toward senior regulatory or compliance leadership roles
- Collaborative working environment with multidisciplinary teams across quality, engineering and commercial functions
- Flexibility and autonomy in managing regulatory projects and stakeholder relationships
- Day rate typically ranging from £250–280 per day through to £750 per day, dependent on experience and contract scope
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