Clinical Technology Specialist
2 weeks ago
Key Responsibilities:
Assess the classification, evaluation, and resolution of adverse incidents and medically related inquiries for products currently in the market.
Make informed decisions regarding the severity, reportability, and potential link of adverse incidents.
Prepare FDA Medical Device Reporting (MDR) and other regulatory documentation for relevant authorities.
Execute various tasks within the post-market surveillance division.
The individual will primarily work on a computer throughout the day and will thrive by effectively managing their time and tasks.
Qualifications:
This is an entry-level position, welcoming recent graduates with relevant internship or capstone project experience.
A degree in biomedical engineering or a related field is preferred, as it will facilitate future career advancement.
0 - 2 years of academic or professional experience is required.
Strong organizational abilities are essential.
The role involves handling complex products; overseeing daily events and qualitative data related to product and patient information received from the field.
Exceptional communication, organizational, attention to detail, and time management skills are necessary.
Proficiency in MS Office Suite, with a basic understanding of Excel, is expected.
Candidates who have balanced work and academic commitments or participated in sports while studying are encouraged to apply.
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