Represent Regulatory Affairs on cross-functional project teams and provide strategic input and technical guidance on product lifecycle planning and regulatory requirements for non-medical devices, and medical devices.
Assess the acceptability of documentation for medical device submissions and effectively communicate regulatory guidance.
Assist in SOP development and review in support of "next-gen " product offerings.
Revisit and compare regulatory outcomes with initial product concepts to make recommendations on future actions.
Understand and investigate regulatory history/background of class, disease/ therapeutic context in order to assess regulatory implications for approval.
Create and ensure maintenance of technical documentation (such as clinical evaluation reports, risk management reports, 510(k) notification) as required for...
★ Ready to Start Your European Career?
Take the next step and apply for this exciting opportunity