Medical Technology Jobs in Exeter

Johnson & Johnson MedTech · Maidenhead

Shapes medical strategy for a portfolio of current and future oncology assets, leading integrated evidence generation, medical education and scientific engagement plans. Serves as a core member of the Cross-Functional Value Team, representing UK medical needs within EMEA and Global forums, and leads, coaches and develops a team of Medical Advisors. Provides medical signatory oversight and ensures compliance with the ABPI Code of Practice.

Johnson & Johnson MedTech · Breda, Netherlands · €68,600 – €119,600 pa

Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedures. Manages vendors handling anonymisation and synthetisation, and acts as the primary contact for YODA Project requests, supporting external research teams using clinical study data.

Johnson & Johnson MedTech · GB019 Bessemer

Supports intraocular lens proctoring and medical information requests, analysing surgical cases and post-operative outcomes to optimise clinical results. Provides expert clinical guidance to healthcare professionals, manages MIR responses within four days, and produces performance reports with Product Safety, Marketing and R&D. Home-office based with up to 20% travel across EMEA.

Johnson & Johnson MedTech · Pratica di Mare, Italy

Supports intraocular lens proctoring and medical information requests to ensure optimal clinical outcomes, analysing sub-optimal results and clinic workflow factors. Manages MIR responses within four days, generates statistics reports, and assists healthcare professionals with post-operative outcome analysis. Home-office based with up to 20% travel, reporting to the Associate Director of Clinical Services.

Johnson & Johnson MedTech · IE009 Janssen Cilag Ltd

Supports intraocular lens proctoring and medical information requests to ensure optimal clinical outcomes, analysing sub-optimal results and clinic workflow factors. Manages MIR responses within four days, generates statistics reports, and assists HCPs with post-operative outcome analysis. Provides clinical expert support for new product introductions, demos and clinical studies, working home-office based with up to 20% travel.

Johnson & Johnson MedTech · Hamburg, Germany · €93,500 – €149,845 pa

Field-based medical affairs role supporting Shockwave Medical's cardiovascular portfolio across Europe. Builds relationships with key opinion leaders, oversees investigator-initiated studies, reviews promotional materials, and provides scientific and HEOR support to cross-functional teams. Requires frequent conference attendance and up to 50% travel.

Johnson & Johnson MedTech · Wokingham · €93,500 – €149,845 pa

Field-based Medical Affairs role supporting Shockwave Medical's cardiovascular portfolio across Europe. Builds relationships with key opinion leaders, supports investigator-initiated studies, reviews promotional materials, and provides scientific and HEOR support to cross-functional teams. Requires frequent conference attendance and up to 50% travel.

Johnson & Johnson MedTech · Machelen, Belgium · €93,500 – €149,845 pa

Field-based Medical Affairs role supporting Shockwave Medical's cardiovascular portfolio across Europe. Involves building KOL relationships, managing investigator-initiated studies, providing scientific and HEOR support, reviewing promotional materials, and representing the company at conferences. Requires close cross-functional work with Clinical, Regulatory, Marketing and Market Access teams.

Johnson & Johnson MedTech · High Wycombe

Independent clinical quality-risk leadership role translating risk signals into proactive mitigation, escalation and inspection/submission readiness across trials and programs. Involves maintaining Clinical Quality Plans, driving quality risk monitoring reviews, supporting CAPA plans, and leading inspection readiness and mock inspections with cross-functional teams.

Johnson & Johnson MedTech · Machelen, Belgium

Leads organizational change management for a multi-year global SAP S/4HANA transformation, harmonizing 40+ ERP systems across MedTech supply chain. Directs business adoption activities including change impacts, communications, training, readiness, role mapping and sustainment, working with programme and value stream leaders to ensure the organization realizes intended value.

Johnson & Johnson MedTech · Wokingham

Leads organizational change management for a multi-year global SAP S/4HANA transformation, harmonizing 40+ ERP systems across MedTech supply chain. Directs a Business Adoption team covering change impacts, communications, training, readiness, role mapping and sustainment, advising programme and business leaders on adoption risks and pace of change.

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.

Johnson & Johnson MedTech · Maidenhead

Leads preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned projects covering content, scientific strategy, timing and tracking, and manages direct reports including hiring, goal-setting and development. Involves mentoring junior writers, overseeing external contractors, and driving departmental process improvements.

Johnson & Johnson MedTech · Beerse, Belgium · €79,800 – €137,770 pa

Leads preparation and finalisation of clinical and regulatory documents for the Immunology therapeutic area within the Regulatory Medical Writing team. Acts as lead writer or point of contact for programmes, guides cross-functional teams, and manages, mentors and develops direct reports in medical writing.

Johnson & Johnson MedTech · Leiden, Netherlands · €68,600 – €119,600 pa

Leads preparation and finalisation of clinical and regulatory documents for the Immunology therapeutic area within the Regulatory Medical Writing team. Acts as lead writer or point of contact for programmes, guides cross-functional teams, and manages, mentors and develops direct reports including hiring and performance discussions.