Analyst, Product Surveillance

Experis, a Manpower Group company, has an exciting contract opportunity for one of our key clients, a Fortune 500 American global biopharmaceutical company that is engaged in the discovery, development, and manufacture of healthcare products. Our client, the medical device manufacturing industry, is seeking an analyst in product surveillance to join their team. 
 
Job Title:  Analyst, Product Surveillance
Location: Plymouth, MN
Pay Range: $30-$35/hr on w2
 
What’s the Job?

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 manager is open to someone with a background and/or degree in Technology or the Sciences If person has 0–2 years of course work or work experience, they will be considered A 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; they must have organizational skills.
I will be working with a complex product, which is a heart pump, to manage the day-to-day events and qualitative data related to product and patient information coming in from the field.
I must have excellent communication, organizational, attention to detail, and time management skills.
I will be using MS office suite with basic Excel working knowledge A person who has juggled a job and school or a sport and school is a good candidate.

Years Experience: 0–2 years
Skills: Related experience in post-market surveillance in a medical device or pharmaceutical industry is preferred.
Education: a four-year degree, preferably in the healthcare or science fields; or a two-year degree and relevant experience supporting complaint handling investigations, medical device reporting, or product analysis. Degreed applicants without medical, scientific, or complaint handling experience may be considered if they possess the strengths suitable for this position.
Duties: May perform multiple functions within the post-market surveillance department. Major responsibilities would include determining classification, review, and disposition of adverse events and medically related complaints for on-market products, including decisions on seriousness, reportability, and potential causality. Complete FDA MDR and other outside competent authority regulatory reports.