This position is primarily responsible for creating line drawings along with entering new orders for product development on the PD schedule, assisting with photography of new samples and assisting with engineering projects. Prepare designs, drawings and layouts working from engineering specifications using computer-aided drafting (CAD) methods. Calculate dimensions, weights, capacities, or ...
Seeking track record in oversight of regulatory submissions for the US, EU and ROW registrations and Quality System compliance processes such as CAPA, change orders, internal audits and adverse issues.
Requires 4+ years of experience in Medical Device Regulatory Affairs for an ISO 13485 environment.
*** Preparing and filing regulatory submissions including registration of ...
Jul 8 -
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