Job Description

Duties:    

• 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 our products manufactured or sold in the US and/or global markets.
• Assists with other regulatory duties as requested.

• Experience in veterinary medicine and/or Pharmacovigilance experience preferred

• RVT or associate degree 

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