Medical Technology Jobs

• Horsham, United States
• Hybrid · 3 days in office
• US$137,000 – US$235,750 pa
• Director · manages people

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.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Titusville, United States
• Hybrid · 3 days in office
• US$137,000 – US$235,750 pa
• Director · manages people

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.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Manchester
• On-site
• £43,200 – £64,800 pa

Field-based role covering the North West, providing clinical and technical support to electrophysiologists, cardiac physiologists and cath lab teams during cardiac ablation procedures using Cryo, PulseSelect and Affera therapies. Involves procedural troubleshooting, product and therapy training, and supporting installations and launches alongside sales and marketing to drive therapy adoption in assigned accounts.

Cryo · PulseSelect · Affera

• 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

• Carlisle
• Remote
• £45,000 – £50,000 pa

Consultative territory sales role selling surgical oncology implants into NHS operating theatres, covering Scotland and northern England. Split roughly 80% new business generation and 20% account development, including quotations, equipment demonstrations and attendance at congresses. Full training and mentoring provided, with trust-based hours and remote working options.

Surgical Implants · Medical Devices · Medical Consumables

• Raritan, United States
• US$105,000 – US$181,700 pa
• Mid-level

Lead pharmacovigilance process and training projects, including process development, mapping, and training qualification and delivery, while acting as a quality partner between business, quality, and governance groups. Support a digital transformation roadmap toward data-centric content and a qualification management system, managing timelines, risks, and audits.

• Titusville, United States
• US$105,000 – US$181,700 pa
• Mid-level

Lead pharmacovigilance process and training projects, including process development, mapping, and qualification delivery, while acting as a quality partner to the Office of the Chief Medical Officer. Drive digital transformation toward data-centric content and qualification management, managing risks, timelines, and audits across a matrixed life sciences organization.

• Raritan, United States
• Hybrid
• US$117,000 – US$201,250 pa
• Mid-level

Leads the development, revision and maintenance of primary labeling documents such as the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues, and contributes to global labeling strategy and continuous process improvement within a matrixed regulatory team.

Company Core Data Sheet (CCDS) · United States Package Insert (USPI) · European Union Product Information (EUPI) +1

• Horsham, United States
• Hybrid
• US$117,000 – US$201,250 pa
• Mid-level

Leads the development, revision and maintenance of primary labeling documents including the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues, and contributes to global labeling strategy and continuous process improvement within a matrixed regulatory affairs team.

Company Core Data Sheet (CCDS) · United States Package Insert (USPI) · European Union Product Information (EUPI)

• Titusville, United States
• Hybrid
• US$117,000 – US$201,250 pa
• Mid-level

Leads the development, revision and maintenance of primary labeling documents including the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, timelines and scientific integrity, resolves labeling issues, and contributes to global labeling strategy and continuous process improvement within a matrix team.

Document Management Systems

• Beerse, Belgium
• Hybrid
• €82,000 – €141,450 pa
• Mid-level

Leads the development, revision and maintenance of primary labeling documents including the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues, and contributes to global labeling strategy and continuous process improvement within a matrix team.

Company Core Data Sheet (CCDS) · United States Package Insert (USPI) · European Union Product Information (EUPI)

• Warsaw, Poland
• Hybrid
• €205,000 – €354,200 pa
• Mid-level

Leads the development, revision and maintenance of primary labeling documents such as the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues and contributes to global labeling strategy and continuous process improvement within a matrix team.

Company Core Data Sheet (CCDS) · United States Package Insert (USPI) · EU Product Information (EUPI) +1

• Allschwil, Switzerland
• Hybrid
• Mid-level

Leads the development, revision and maintenance of primary labeling documents including the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues and contributes to global labeling strategy and continuous process improvement within a matrix team.

Company Core Data Sheet · United States Package Insert · EU Product Information

• Zug, Switzerland
• Hybrid
• Mid-level

Leads the development, revision and maintenance of primary labeling documents including the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues, and contributes to global labeling strategy and continuous process improvement within a matrix team.

• Bern, Switzerland
• Hybrid
• Mid-level

Leads the development, revision and maintenance of primary labeling documents including the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues and contributes to global labeling strategy and continuous process improvement within a matrix team.