Medical Devices Clinical Safety Team Member

An exciting opportunity is open for an experienced Medical Devices Clinical Safety professional to support a leading global organisation in driving the safe development and oversight of medical devices and in-vitro diagnostics. Operating at the forefront of innovation, this organisation is dedicated to enhancing patient outcomes through robust safety processes and a commitment to continuous improvement.

This contract position offers the chance to work across diverse portfolios, collaborating with multifunctional and multicultural teams, and engaging with regulatory authorities and key external stakeholders. It's an ideal role for a specialist who thrives in complex environments and wants to apply their expertise where it truly matters.

Your role as Medical Devices Clinical Safety Team Member

• Serve as a core member of the Clinical Safety Team for medical devices, actively contributing to critical safety discussions and strategy.

• Lead or support the creation, refinement, and rollout of safety processes and procedural documents, driving improvements based on compliance metrics, audit findings, and stakeholder feedback.

• Act as a subject matter expert or process owner in areas such as business process optimisation and global safety initiatives.

• Provide expert consultation on medical device safety matters to internal safety teams, including considerations for third-party manufactured devices.

• Help deliver and facilitate training on standard operating procedures and safety processes related to medical devices.

• Engage with cross-functional groups and global expert committees to shape the external landscape and stay ahead of evolving device safety standards.

Experience and qualifications for the Medical Devices Clinical Safety Team Member role

• Background in healthcare, life sciences or biomedical research, combined with hands-on experience in clinical safety for medical devices, in-vitro diagnostics or combination products.

• Strong knowledge of medical device regulations and industry quality standards.

• Demonstrated ability to develop or enhance safety processes and influence cross-functional teams in a matrix environment.

• Confident communicator who can effectively build consensus across diverse teams and stakeholders.

• Up-to-date understanding of the technical and scientific aspects of medical devices, with a commitment to integrating device activities into broader pharmacovigilance frameworks.

• Experience contributing to audits, inspections, or due diligence activities related to medical device safety is highly desirable.

For immediate consideration for this contract Medical Devices Clinical Safety Team Member position - or to explore similar opportunities in the medical device and pharmaceutical safety space - please apply or reach out today.