Pharmacovigilance Quality Specialist

5 hours ago


Liverpool, Liverpool, United Kingdom RRxCo.™ Full time

RRxCo. is seeking an experienced Pharmacovigilance Quality Auditor/Consultant to support several Biotechnology Sponsors in their regulatory compliance and quality assurance initiatives.

The projects will be delivered remotely with possible travel to the United States and mainland Europe.

Key Responsibilities:

  • Conduct audits and inspections to ensure compliance with Good Pharmacovigilance Practices (GVP) and global regulations
  • Provide strategic advice and operational execution to clients across various biotechnology sectors
  • Evaluate supplier performance and capabilities
  • Analyze data and provide insights to inform business decisions
  • Collaborate with cross-functional teams to achieve project goals

Requirements:

  • In-depth experience of GVP and auditing against UK, US, and EU regulatory requirements
  • Proven track record of delivering high-quality services and ensuring client satisfaction
  • Ability to work independently and as part of a team
  • Familiarity with small molecules, large molecules, and advanced therapies
  • Strong analytical and problem-solving skills

Estimated Salary: $120,000 - $180,000 per year, depending on experience and qualifications

About RRxCo.: As a leading provider of pharmacovigilance services, we are committed to helping our clients navigate complex regulatory landscapes and ensure the highest standards of quality and safety.



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