GVP/GPvP Compliance Specialist

2 weeks ago


Liverpool, Liverpool, United Kingdom RRxCo.™ Full time
Job Description

We are seeking a skilled Pharmacovigilance (GVP/GPvP) Quality Auditor/Consultant to support our Biotechnology Sponsors in their strategic advisory needs, project execution, and supplier audits.

About the Role
  • The ideal candidate will have in-depth experience of Good Pharmacovigilance Practices.
  • Proven auditing expertise across the globe against both UK and US regulatory requirements, with EU knowledge being advantageous.
  • A strong background in working across various technologies, including small molecules, large molecules, and advanced therapy.
  • Ability to provide strategic and operational execution as part of a comprehensive program of work.
  • Flexibility to adapt to project requirements and comfort with scaling up or down services.
Key Responsibilities
  1. Support our Biotechnology Sponsors with strategic advice on Pharmacovigilance practices.
  2. Execute projects remotely, with occasional travel to the United States and mainland Europe.
  3. Audit suppliers to ensure compliance with regulatory requirements.
  4. Provide strategic and operational execution as part of a wider program of work.
Requirements
  • Strong experience in Pharmacovigilance practices.
  • Proven auditing skills across multiple regions.
  • Background in working with various technologies.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and as part of a team.
Salary and Benefits

Estimated salary: $120,000 - $150,000 per annum. We offer a competitive package, including benefits, to attract top talent in the industry.



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