Collecting information
Organizing data
This role involves leading risk management activities across product lifecycles in the medical devices sector, ensuring compliance with standards. The ideal candidate will have over 8 years of experience in a regulated industry, particularly medical devices, and a solid educational background in eng
Quality Engineer Level 3 – Risk Management to lead risk management across devices and diagnostics from development through post-market. You will collaborate with Quality, Regulatory, R&D, Manufacturing and Post-Market teams to ensure risk controls meet FDA, ISO 13485, ISO 14971 and other regulator
Medical Director/Senior Medical Director, Clinical Development (Prostate). The Medical Director will work in close partnership with cross-functional teams including Clinical Operations, Regulatory Affairs, Biostatistics, Safety/Pharmacovigilance, Translational Medicine, and Medical Affairs. This rol
Works collaboratively with the other members of the clinical research team and the clinical and administrative support teams to ensure all protocols are followed and that there is timely documentation and submission of study data. Two years' experience in a clinical research setting, working in on I
Employee share purchase scheme Bi-annual Profit share Life, Critical illness and Income Protection Insurance Discounted Health Insurance Active Social clubs & community groups In-house training programs from external providers Purchasing privileges for Fisher & Paykel Healthcare and Medela pro