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Biomedical Engineer

Contract: Burlington , Massachusetts, US

Salary: $30.00 Per Hour

Job Code: 352456

End Date: 2024-09-05
Days Left: 20 days, 3 hours left

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Responsibilities:

• Determine classification, review, and disposition of adverse events and medically related complaints for on-market products
• Make decisions on seriousness, reportability, and potential causality of adverse events
• Complete FDA MDR and other outside competent authority regulatory reports
• Perform multiple functions within the postmarket surveillance department
• Person will be in-front of a computer for the entire day and will be successful if they can manage their time effectively and efficiently

Required:

• Entry-level role - will accept fresh college graduates with internship or capstone project work.
• Someone with a biomedical degree would be a good fit as this will allow for future opportunities
• 0 - 2 years of course work or work experience
• Must have organizational skills.
• Will be working with a complex product; managing the day-to-day events and qualitative data related to product and patient information coming in from the field
• Must have excellent communication, organizational, attention to detail, and time management skills;
• Will be using MS office suite with basic Excel working knowledge
• A person that has juggled a job and school or a sport and school is a good candidate.

Job Requirement

• FDA
• MDR
• Excel
• MS office
• Biotech
• postmarket surveillance
• Entry Level

Reach Out to a Recruiter

• Recruiter
• Email
• Phone
• Sanjay Rawat
• [email protected]

Apply Now

Job Tags

Hourly pay, Contract work, Work experience placement, Internship,

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