Strong administration skills and attention to detail.
Analytical and problem-solving skills.
Ability to work independently and collaboratively, and ability to prioritise and plan tasks.
Competent in Microsoft Office products.
Fluent in written and spoken English
Advanced MS Excel skills (e.g. VLOOKUP, Pivot Table analysis).
Demonstrates understanding of navigating medical device regulations and regulatory guidance for regulatory submissions in MDSAP markets and/or the EU.
Qualified internal auditor with experience of performing internal and/or supplier audits to ISO 13485, MDSAP requirements, the EU MDR and/or ISO 9001.
2 years’ experience with Trend Analysis.
Vision RT is an Equal Opportunity
all qualified applicants will receive consideration for employment and development without regard to race
or protected veteran status.
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Post-Market Surveillance (Complaints) Specialist

Summary