Pharmacovigilance & QA
hace 4 días
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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