Medical Technology Jobs

Johnson & Johnson MedTech · Raritan, United States · US$137,000 – US$235,750 pa

Leads the Accelerando program management function, partnering with high-priority new product development teams to de-risk and accelerate clinical trial execution. Acts as a trusted advisor to Compound Development Teams, running critical path analysis, threat and opportunity assessments, and project planning in Planisware and MS Project. Also leads a team, drives best-practice adoption and benchmarking across a global matrix organisation.

Johnson & Johnson MedTech · Zug, Switzerland

Leads organizational change management for a multi-year global SAP S/4HANA transformation, harmonizing 40+ ERP systems across MedTech supply chain. Accountable for change strategy, communications, training, readiness, role mapping and sustainment, working with programme and business leaders across regions and value streams.

Smith & Nephew · Hull

Owns end-to-end global supply and distribution planning for an assigned product portfolio, building monthly and weekly plans for factories, GDCs and LDCs. Monitors service, backorders and stock coverage, escalates supply risks into S&OE and SIOP/IBP, and works across demand planning, procurement, quality and manufacturing in a global matrix.

Smith & Nephew · UK - Field

Field-based sales role covering the London territory, promoting a medical technology portfolio to NHS and private customers. You build relationships, follow up leads, provide product training and technical advice, and track competitor activity and market trends. Suits a new graduate or someone with clinical skills moving into a commercial career.

Medtronic · London · £76,800 – £115,200 pa

Builds and maintains modern C++ (C++17+) application software for intra-operative surgical devices, working in a multidisciplinary team spanning embedded, cloud and application software. Responsibilities include device monitoring, cloud connectivity, debugging, and developing secure, medical-grade code compliant with regulatory and security processes.

Medtronic · London · £76,800 – £115,200 pa

Designs, builds and maintains AWS and on-prem infrastructure used by ML engineers, data scientists and product teams, with a strong focus on Kubernetes, GitOps, Terraform and Docker. The role sits in the Surgical AI Centre of Excellence, supporting an MLOps platform for connected operating-room products, and requires two days a week in London.

Johnson & Johnson MedTech · Limerick, Ireland

Supports intraocular lens proctoring and medical information requests, analysing surgical cases and post-operative outcomes to optimise clinical results. Collaborates with product safety, marketing, R&D and commercial teams, providing expert support to healthcare professionals and internal customers on new product introductions. Home-office based with up to 20% travel across EMEA.

Johnson & Johnson MedTech · Toronto, Canada · CA$87,000 – CA$140,300 pa

Writes and coordinates clinical and regulatory documents such as CSRs, IBs, protocols, summary documents, RMPs and briefing documents for oncology programmes. Leads cross-functional document planning and review meetings, sets timelines and strategies, and mentors junior writers while acting as lead writer on most compounds. Hybrid role with three days onsite weekly.

Johnson & Johnson MedTech · Raritan, United States · US$137,000 – US$235,750 pa

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare regulatory safety analyses and benefit-risk evaluations. Supports Safety Management Teams, chairs proactive safety data reviews, and acts as product SME for audits and health authority interactions.

Johnson & Johnson MedTech · Horsham, United States · US$137,000 – US$235,750 pa

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare analyses and evaluations for regulatory compliance. Supports Safety Management Teams, chairs proactive safety data reviews, and acts as product or process subject matter expert for audits and health authority interactions.

Johnson & Johnson MedTech · Titusville, United States · US$137,000 – US$235,750 pa

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare regulatory safety analyses and evaluations. Supports Safety Management Teams, conducts proactive safety data reviews, and serves as product point of contact, with oversight of deliverables prepared by other team members.

Johnson & Johnson MedTech · Maidenhead

Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance, and safety-native architecture. You will design reproducible experiments, prototype layered safeguards, publish results, and work with platform engineers to move validated methods into a GenAI platform.

Johnson & Johnson MedTech · Limerick, Ireland

Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance and safety-native architecture. Hands-on work prototyping and validating methods on real GenAI platform workflows, publishing results and handing validated approaches to engineering partners.

Johnson & Johnson MedTech · Beerse, Belgium

Lead a two-year postdoctoral research program on making agentic AI safe for regulated pharmaceutical R&D, covering provable controls, adversarial assurance, and safety-native architecture. You will design reproducible experiments, prototype layered architectures, and work with platform engineers to move validated methods into a GenAI platform. The role is hands-on research with real systems as the testbed, not frontier model pre-training or production engineering.

Johnson & Johnson MedTech · Leiden, Netherlands

Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, continuous adversarial red-teaming, and safety-native architecture. Hands-on work prototyping and validating methods on real GenAI platform workflows, publishing results, and transitioning validated approaches into production with engineering partners.