Job Description

Hybrid; 3 days onsite in either St. Joseph, MO or Duluth, GA
Remote? No
Full time or part time? Full time or part time (25-40 hours)
Shift Daytime
Hours 8am-5pm CST M-F
Number of Positions 1 or 2 - depending on full time or part time interest
Any possibility of the assignment to be converted to a full-time role? Not at this time.
Supports the complaint handling processes to ensure compliance with all competent authorities (including but not limited to FDA, USDA-APHIS, EMA, CFIA etc..) as described in the corporate and *** PV SOPs, FDA 21 CFR, USDA 9 CFR, and current European regulations. Performs data quality review of adverse events for *** products manufactured or sold in the US and/or global markets.
Assists with other regulatory duties as requested.


Experience Experience in veterinary medicine and/or Pharmacovigilance experience preferred


RVT or associate degree

Job Tags

Full time, Shift work,

Similar Jobs