In addition, the Regulatory Affairs Specialist will perform activities associated with PMS, including Post Market Clinical Follow-Up (PMCF), and Clinical Evaluation Plans and Reports (CEPs, CERs). NPI: The Regulatory Scientist 2 helps develop regulatory strategies, performs activities associated with obtaining and maintaining regulatory approval to commercialise medical devices in selected target markets. […]
Reporting to: Clinical & Post Market Surveillance: Senior Manager Post Market Surveillance, Regulatory Affairs or NPI: Principal Regulatory Scientist Responsibilities Clinical & Post Market...