Pharmacovigilance & QA

hace 4 días


Barcelona, Barcelona, España Oxford Global Resources A tiempo completo

Oxford Global Resources is looking for a Pharmacovigilance & Quality Assurance Consultant to support our client's Global Quality & Compliance team within Veterinary Medicine R&D (VMRD).

  • 100% remote position
    , with occasional travel to Olot or internationally for audits (not frequent).

This is a fantastic opportunity for an experienced QA/PV professional to join a global organization and provide high‑impact support across pharmacovigilance, clinical and non‑clinical programs for veterinary products.

Key Responsibilities

  • Ensure strong understanding and application of current pharmacovigilance regulatory requirements for veterinary products
  • Perform PV quality assurance audits and inspections (VMRD processes, country offices, distributors)
  • Assess regulatory requirements for research supporting registration of animal health products in major global markets
  • Manage CAPAs, deviations and change management related to PV audits
  • Conduct QA audits of non‑clinical and clinical studies, including protocols, data listings, study reports, investigator sites and CROs
  • Participate in QA meetings, document reviews and consultations with VMRD teams

Profile

  • Master's degree in Pharmaceutical Sciences, Biotech or Life Sciences
  • 3–5 years of experience in the biotech/pharma industry
  • Solid knowledge of PV and QA for veterinary products
  • Experience with regulatory requirements, GMP, and interactions with Health Authorities
  • Strong English communication skills; other European languages (Spanish, Portuguese) are a plus

If you have experience in veterinary pharmacovigilance, QA auditing and regulatory compliance, and you're looking for a flexible and impactful role, I'd be happy to share more details.

Feel free to reach out



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