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Postmarket Surveillance Analyst

In Massachusetts / United States

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Postmarket Surveillance Analyst   

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JOB TITLE:
Postmarket Surveillance Analyst
JOB TYPE:

JOB SKILLS:
JOB LOCATION:
Burlington Massachusetts / United States

JOB DESCRIPTION :
Postmarket Surveillance Analyst
8:00AM-5:00PM
Pay Rate: $33.33/HR

Cortech is seeking a Postmarket Analyst for our client in Burlington, MA.


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 24, 2021
S16204860623801449
Massachusetts / United States
Burlington
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Postmarket Surveillance Analyst    Apply

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Postmarket Surveillance Analyst
8:00AM-5:00PM
Pay Rate: $33.33/HR

Cortech is seeking a Postmarket Analyst for our client in Burlington, MA.


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