What are the responsibilities and job description for the Product Surveillance Analyst position at TekOne IT Services Pvt. Ltd.?
Hello This is Komal from Intellectt we have an opening for a Product Surveillance Analyst in St. Paul, MN. Please find the job details and description below and if interested You can reach me at komal@intellectt.com or call me at 1(732)-813-9025.
Role: Product Surveillance Analyst
Location: St. Paul, MN - 55117
Duration: 12 Months
Shift Timings: 8 AM to 5 PM
Job Description
Years Experience: 0 - 2 years
Skills: Related experience in post market surveillance in a Medical Device or Pharmaceutical Industry preferred.
Education: Four-year degree, preferably in the healthcare or science fields; or 2-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 postmarket 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 report
Role: Product Surveillance Analyst
Location: St. Paul, MN - 55117
Duration: 12 Months
Shift Timings: 8 AM to 5 PM
Job Description
Years Experience: 0 - 2 years
Skills: Related experience in post market surveillance in a Medical Device or Pharmaceutical Industry preferred.
Education: Four-year degree, preferably in the healthcare or science fields; or 2-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 postmarket 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 report
