Veterinarian Pharmacovigilance Specialist

Meet Life Sciences; Saint Joseph (MO); Presencial; USD 70 000 - 110 000; Tempo integral

Resumo da oferta

An established industry player in pharmaceutical manufacturing is seeking a dedicated Veterinarian Pharmacovigilance Specialist. This role is crucial for ensuring compliance with regulatory authorities regarding adverse event reporting and product safety. The specialist will review and assess product complaints, maintain accurate records, and support pharmacovigilance management in analyzing adverse drug events. If you have a DVM or VMD degree and a passion for ensuring product safety, this is an exciting opportunity to make a significant impact in a dynamic environment.

Qualificações

• DVM or VMD degree from an accredited veterinary college required.
• 3+ years of experience in veterinary practice or pharmacovigilance.

Responsabilidades

• Review and assess adverse event and product complaints for compliance.
• Submit adverse events to regulatory authorities as per SOPs.

Conhecimentos

Analytical Skills

Regulatory Compliance

Pharmacovigilance Knowledge

Adverse Event Analysis

Formação académica

DVM or VMD degree

Descrição da oferta de emprego

Veterinarian Pharmacovigilance Specialist

The Pharmacovigilance Specialist ensures compliance with all relevant regulatory authorities (FDA, USDA-APHIS, EMA, CFIA, etc.) regarding adverse event reporting and product safety. This role involves reviewing, assessing, and approving product/adverse event complaints for BIAH products, ensuring adherence to corporate and regulatory guidelines (including FDA 21 CFR, USDA 9 CFR, and European regulations). Additionally, the specialist may assist PV management in analyzing adverse drug events (ADEs), trending data, and supporting signal detection efforts.

Responsibilities:

• Review and assess adverse event and product complaints for products, ensuring compliance with regulatory requirements.
• Submit relevant adverse events to competent authorities (e.g., FDA, USDA, EMA, CFIA) in accordance with SOPs and applicable regulations.
• Ensure full compliance with pharmacovigilance regulations (FDA, USDA, EMA, etc.) and relevant corporate SOPs, including the timely reporting of adverse events and product complaints.
• Provide support to Pharmacovigilance Management in adverse drug event (ADE) analysis, trending, and signal detection as part of ongoing product safety monitoring.
• Maintain accurate records of adverse events and product complaints, ensuring proper documentation in compliance with regulatory and company standards.

Qualifications:

• DVM or VMD degree from an accredited veterinary college.
• Minimum of 3 years of veterinary practice experience or relevant experience in pharmacovigilance, pharmacoepidemiology, or a related field.
• In-depth understanding of pharmacovigilance regulations and compliance requirements (FDA 21 CFR, USDA 9 CFR, European regulations).
• Strong analytical skills and experience with adverse event analysis, trending, and signal detection.

Seniority level

Associate

Employment type

Contract

Job function

Other

Industries

Pharmaceutical Manufacturing