Medical Technology Jobs

• Beerse, Belgium
• Senior

Combines rigorous statistical thinking with modern AI to build validated, reusable AI-enabled statistical solutions for pharmaceutical research and manufacturing. Hands-on work spans Python services, LLMs, RAG, agentic workflows, APIs and MCP, ensuring statistical integrity, reproducibility and traceability in a regulated environment.

Python · R · SQL +7

• Leiden, Netherlands
• Senior

Develops trustworthy, validated AI-enabled statistical solutions for pharmaceutical research and manufacturing, working at the intersection of biostatistics, AI and scientific software development. Builds Python services, connects R and Python tools via APIs and MCP, and creates agentic workflows using LLMs and RAG. Ensures statistical integrity, reproducibility and governance in a regulated environment.

Python · R · SQL +7

• London
• Remote
• £124,800 – £187,200 pa
• Director · manages people

Leads commercial growth and adoption of connected care and digital health solutions across Western European hospital systems, negotiating multi-year enterprise partnerships and guiding product launches. Manages a growing team and works with clinical, IT and executive stakeholders on interoperability, analytics and monitoring platforms. Remote with around 70% regional travel.

HL7 · FHIR · APIs +2

• Berlin, Germany
• Remote
• €156,000 – €234,000 pa
• Director · manages people

Leads commercial growth and adoption of connected care and digital health solutions across Western Europe, structuring multi-year enterprise partnerships with hospital systems. Manages a growing team and works with clinical, IT and executive stakeholders on interoperability, monitoring and data integration. Remote with around 70% regional travel.

HL7 · FHIR · APIs +2

• United Kingdom, YY9 9YY
• Remote
• Mid-level

Provides day-to-day medical oversight for one or more clinical trials, ensuring patient safety, data integrity and protocol compliance. Reviews and assesses AEs and SAEs, supports safety signal detection with Pharmacovigilance, and advises investigators on eligibility and dosing. Works cross-functionally with Clinical Operations, Data Management, Biostatistics and Regulatory Affairs, and contributes to CSRs and regulatory submissions.

Data Safety Monitoring Boards

• Welwyn Garden City
• £377 – £500 ph
• Mid-level
• Contract

Coordinate early-phase clinical trials within a pharmaceutical Clinical Operations team, covering study start-up, feasibility, timelines, recruitment and vendor oversight. Maintain TMF documentation, risk logs and regulatory compliance under ICH-GCP while working with Data Management, Regulatory Affairs and external partners.

Trial Master Files · Microsoft Office

• United Kingdom - Remote Based
• Remote
• £53,410 – £83,930 pa
• Lead · manages people

Leads a team of 20+ clinical consultants delivering Radiology Informatics implementations across the UKI and Nordics, validating solution design against customer clinical needs during presales and guiding C-level stakeholders through sales, implementation and adoption. Coaches the team and sales resources on vuePACS and vueRIS, drives methodology development, and acts as an active member of the European Clinical Consulting community.

vuePACS · vueRIS

• Sheffield
• Hybrid
• £32,000 pa
• Mid-level
• Permanent

This role involves driving sales of medical devices through a consultative, virtual-first approach, combining clinical and technical expertise with strong account management. The candidate will identify customer needs, deliver product solutions, and develop strategic business plans to grow both existing and new accounts. Success requires analytical insight, proactive market awareness, and effective communication across video, phone, and in-person channels.

• Milton Keynes
• Hybrid · 3 days in office
• £58,000 pa
• Mid-level · manages people
• Temporary

Lead a multi-disciplined team covering quality, health & safety, environment, information security and regulatory compliance at a top 10 global life science business. Own the ISO 9001 and ISO 14001 systems, run risk-based internal and external audit programmes, and use quality data and KPIs to shape strategy, presenting to senior leadership. An 18-month fixed term contract covering maternity leave.

ISO 9001 · ISO 14001 · ISO 13485 +7

• Saffron Walden
• £30 – £33 ph
• Contract

Hands-on testing and validation of medical devices, including stress and force testing in a lab environment. The role involves analysing data for design verification, developing new test procedures, and documenting all technical activity to regulatory and quality standards. It sits within a test team on a high-impact medical device project.

• United Kingdom
• £55,000 – £70,000 pa

This role involves leading and executing in-vitro toxicology studies, including Neutral Red, Ames, and micronucleus assays, within a regulated laboratory environment. The scientist will develop and optimise testing methodologies, interpret complex biological data, and support regulatory submissions. They will work collaboratively across multidisciplinary teams and with external partners to advance pre-clinical testing capabilities in product safety assessment.

• Leeds
• £45,000 – £55,000 pa
• Lead · manages people

Lead and coordinate the PM shift Chemistry and Microbiology laboratory team, managing daily workloads, performance and training. Oversee testing such as HPLC analysis, bioburden and environmental monitoring, ensuring compliance with cGMP and ISO 13485 while driving investigations, validation and continuous improvement.

HPLC

• Stirling
• On-site
• £25 – £27 ph
• Senior
• Contract

Execute complex experimental workstreams from concept through to design transfer, analysing multi-factorial data and presenting technical findings to stakeholders. Apply Design for Manufacture principles to optimise product formulations and characterisation, while upholding GLP, GMP and GDP compliance in a fully site-based laboratory. Requires diagnostic immunoassay expertise, ideally with particle-based assays and fluorescent detection.

• London
• Remote
• Mid-level

Manages a portfolio of clinical research studies end to end, leading cross-functional teams and client relationships to deliver Patient Cloud projects on time and within budget. Involves risk assessment, study documentation, and meetings, with expertise in eCOA/ePRO, eConsent, virtual trials or wearables. Fully remote, but requires flexibility to work American time.

MS Office Suite · Google Workspace

• Maidenhead
• Director · manages people

Leads the global labelling function for an influenza vaccine portfolio, owning the end-to-end review and approval process and setting labelling strategy across regions. Chairs the Global Labelling Committee, sits on the regulatory leadership team, and manages time-critical annual strain updates while representing the company in external regulatory forums.