Postmarket Surveillance Analyst I job in Plymouth, MN
Vacancy has expired
Plymouth, MN CorTech LLC
| Job Ref: | 346213 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 35.68/Per Hour |
| Remote: | No |
Location |
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| City: | Plymouth, MN |
| Post Code: | 55442 |
| Map: |
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Description |
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CorTech is seeking to hire a Postmarket Surveillance Analyst I for our client in Plymouth, MN! Benefits Available! Weekly Pay! $35.68/Hour Start Time (AM/PM) 8:00 AM End Time (AM/PM) 4:30 PM Exempt/Non Exempt: Non Exempt Years Experience: 0-2 years Skills: relevant experience supporting complaint handling investigations, medical device reporting, product evaluation, or related work. Knowledge of global regulations for medical device reporting and medical terminology is a plus Education: Four-year degree, preferably in the healthcare, science, or technical fields; or 2-year degree and 10 years of relevant experience supporting complaint handling investigations, medical device reporting, product evaluation, or related work Duties: Analyst may perform two different functions within complaint handling. One role is that of complaint investigation management which includes all activities pertaining to receiving and investigating reports of worldwide complaints/events on a variety of products; entering information into the complaint database; independently determining and filing appropriate medical devices reports with various regulatory agencies; participating on cross-functional teams; and providing information on product complaints to various teams (e.g. Regulatory, Quality Engineering). Quality experience Medical Field Work Experience 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 | |
ref: (346213)
1052 days ago
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