Medical Technology Jobs

• 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.

• Leeds
• Senior

Hands-on role performing verification and investigational testing of orthopedic implants and instrumentation, developing test methods, fixtures and protocols for regulatory submissions. Works closely with R&D and Quality, contributes to design and process FMEAs, and leads departmental work instructions and audit support.

Load Cells · LVDT · Strain Gages +5

• Blackpool
• On-site
• Lead · manages people

Frontline leadership role on a manufacturing shop floor, supervising daily production output, allocating headcount and resources, and resolving problems to root cause. Drives continuous improvement through Lean and Process Excellence, enforces GMP, and manages performance, absence and disciplinary matters within a regulated orthopaedics environment.

Resource Scheduler

• Blackpool
• Entry level

Two-year graduate development programme comprising four six-month rotations across functions such as process engineering, continuous improvement, production operations, R&D and quality. Graduates own real projects supporting new product and process introductions, testing and continuous improvement, with mentoring and cross-functional networking in a medical devices environment.

Microsoft Office · CAD

• Blackpool
• Mid-level

Owns and optimises assigned manufacturing value streams to ensure safe, compliant and cost-effective production of medical devices. Provides technical leadership, directs complex process development and validation programmes (IQ, OQ, PQ), leads continuous improvement initiatives and mentors junior engineers while representing Engineering in governance and regulatory forums.

Siemens · Rockwell · HMI +1

• Maidenhead
• Hybrid · 3 days in office
• 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, conducts proactive safety data reviews, and acts as product point of contact, with hybrid working requiring three days on site.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Prague, Czech Republic
• Hybrid
• CZK 704,000 – CZK 1,135,050 pa
• Mid-level

Supports end-to-end medical coding of clinical trial data, ensuring consistent, accurate and reproducible coding aligned with regulatory and industry standards. Maintains global thesauri and dictionary encoding systems (MedDRA, WHO Drug), handles coding specifications, quality reviews and sign-off, and advises cross-functional partners on coding issues.

MedDRA · WHODrug

• Leeds
• Hybrid
• Entry level
• Internship

Supports a Clinical Operations team in the day-to-day coordination of clinical studies, maintaining the Trial Master File (TMF/eTMF), tracking activities in CTMS, generating reports and distributing study supplies and regulatory documentation. A student placement offering hands-on exposure to clinical research processes and systems, working with study teams, project managers and site managers. Based in Leeds with flexibility to work remotely, though onsite working is preferred.

Microsoft Office · Microsoft Excel · Microsoft Word +4

• Allschwil, Switzerland
• Mid-level

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

• High Wycombe
• Mid-level

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

• Beerse, Belgium
• €81,400 – €140,530 pa
• Mid-level

Leads Pharmacovigilance process and training projects, including process development, mapping, and training qualification and delivery. Acts as a quality partner for the Innovative Medicines Office of the Chief Medical Officer, linking business partners, quality groups, and governance while supporting a digital transformation toward data-centric content and qualification management. Manages timelines, risks, and audits or inspections.

• Horsham, 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. Act as a quality partner linking business partners, quality groups, and governance, supporting a digital transformation toward data-centric content and qualification management. Manage timelines, risks, and audits within a matrix organization.

ISO 9001

• 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.

• Leeds
• Lead · manages people

Leads the design and execution of professional education for the UK, building scalable learning pathways for healthcare professionals and governing onboarding, events, grants and cadaveric training. Manages a team and external partners including faculty and facilities, partnering with sales, marketing and compliance to close capability gaps and track programme effectiveness.

Amex