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Analyst II, Postmarket Surveillance

In Minnesota / United States

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Analyst II, Postmarket Surveillance   

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JOB TITLE:
Analyst II, Postmarket Surveillance
JOB TYPE:

JOB SKILLS:
JOB LOCATION:
St. Paul Minnesota / United States

JOB DESCRIPTION :
Analyst II, Postmarket Surveillance
Pay Rate: $21.42/HR
8:00am-4:30pm

Cortech is seeking a Postmarket Surveillance Analyst in St Paul, MN.

Job Description:
--Initiates and manages the complaint file, maintains accurate entry of complaints in the database, communicates to field representatives regarding information needed specific to product complaints (e.G. physicians, hospital personnel, sales representatives, international offices), independently assesses the complaint to determine if a medical device report needs to be filed with various global regulatory agencies (e.g. FDA, ECA) and submits reports within required timeframe, diligent of any unusual trends in product complaints and communicates them with mgmt., complies with US FDA regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments, Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors.
--Performs other related duties and responsibilities as assigned

Position Details

Jun 16, 2021
S16204860758473972
Minnesota / United States
St. Paul
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Analyst II, Postmarket Surveillance    Apply

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Analyst II, Postmarket Surveillance
Pay Rate: $21.42/HR
8:00am-4:30pm

Cortech is seeking a Postmarket Surveillance Analyst in St Paul, MN.

Job Description:
--Initiates and manages the complaint file, maintains accurate entry of complaints in the database, communicates to field representatives regarding information needed specific to product complaints (e.G. physicians, hospital personnel, sales representatives, international offices), independently assesses the complaint to determine if a medical device report needs to be filed with various global regulatory agencies (e.g. FDA, ECA) and submits reports within required timeframe, diligent of any unusual trends in product complaints and communicates them with mgmt., complies with US FDA regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments, Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors.
--Performs other related duties and responsibilities as assigned