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Irfa******
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Australia
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Last Update: 09.01.2019 at 12:00
Job Type
Full Time
Start
ASAP
Duration
6 Month +
Place
Sydney
Country
Australia
Category
Regulatory, Quality, and Clinical
Description
The role would be combined with support to the Regulatory Affairs Manager in post -market activities including
Medical device Recall co-ordination
Adverse event and Medical Device Incident reporting (IRIS)
Personal attributes required for this role would include high attention to detail, resilience and demonstrated successes in building strong external and internal relationships through effective communication, influencing and collaborative networking skills.