Overview
Quality Assurance Specialist Jobs in Minnesota, United States at Real Staffing
Title: Quality Assurance Specialist
Company: Real Staffing
Location: Minnesota, United States
MDR Specialist
Note: We do not hire C2C
This position is highly likely to transition to a permanent role after the first year of employment.
Skills and Qualifications:
Strong attention to detail, as accuracy is critical (missing one word could make a significant difference).
Excellent written communication skills, with the ability to thoroughly read and interpret source documentation.
Proficient in evaluating complaints and inputting information into complaint handling systems.
Ability to determine if a complaint needs to be reported to the FDA.
Effective written and verbal communication skills for sometimes reaching out to patients or device representatives.
Independent worker who does not require extensive supervision.
Strong documentation skills with a focus on quality and efficiency.
Primary Responsibilities:
Review complaints and adverse drug reactions for potential reporting to the FDA.
Improve the quality and proficiency of file processing.
Input and code complaint data into the complaint handling systems.
Occasionally communicate with patients or device representatives to gather additional information.
Ensure all documentation is accurate and complete, maintaining high standards of quality.
Key Attributes:
Detail-oriented with a meticulous approach to documentation.
Capable of making independent decisions regarding FDA reporting.
Ability to identify and implement ways to enhance quality and efficiency in file processing.
Strong organizational and time management skills.