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Senior Pv Auditor

2+ years
Not Disclosed
10 April 24, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Senior PV Auditor
Location: Remote
Employment Type: Full-time
Department: PV QA


About the Company:

PrimeVigilance, part of the Ergomed Group, is a specialized mid-size pharmacovigilance service provider founded in 2008. With a global presence across Europe, North America, and Asia, PrimeVigilance delivers services in Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance. The company maintains long-standing partnerships with clients of all sizes and operates across all therapy areas, including medical devices.

PrimeVigilance is committed to employee development, mental well-being, and a healthy work-life balance, ensuring top-tier client services by nurturing a positive and growth-oriented work environment.


Job Responsibilities:

  • Plan, conduct, and lead complex pharmacovigilance audits (internal processes, systems, external partners)

  • Execute contracted audits and QA consultancies for clients, including affiliate or partner systems

  • Develop and implement risk-based audit strategies and annual audit plans

  • Analyze audit outcomes, identify trends, and recommend process enhancements

  • Prepare and present comprehensive audit reports to senior management

  • Collaborate across departments to ensure prompt resolution of audit findings

  • Stay abreast of global pharmacovigilance regulatory updates and best practices

  • Guide and mentor junior auditors and QA team members

  • Participate in regulatory inspections and assist in regulatory responses

  • Contribute to the ongoing development and refinement of PV quality management systems

  • Oversee multiple audit projects, ensuring quality and adherence to timelines


Required Qualifications:

  • Bachelor's degree in Pharmacy, Life Sciences, or a related field (Master’s degree preferred)

  • Extensive experience in pharmacovigilance auditing, including U.S. audit experience

  • Strong knowledge of global PV regulations (EMA, FDA) and Good Pharmacovigilance Practices (GVP)

  • Demonstrated expertise in internal and external audits within the pharmaceutical sector

  • Proficient in risk assessment and audit project management

  • Advanced skills in data analysis, audit reporting, and presentation

  • Familiarity with pharmacovigilance databases and auditing tools

  • Relevant certifications (e.g., RAPS, DIA) are a strong asset

  • Strong analytical mindset and high attention to detail

  • Excellent communication and teamwork skills

  • Ability to manage multiple tasks independently in a dynamic environment

  • Willingness to travel up to 25% for on-site audits, as necessary


What We Offer:

  • Internal training and career development opportunities

  • Emphasis on personal and professional growth

  • Supportive and collaborative global work environment

  • Daily interaction with colleagues across continents, with English as the working language

  • A culture built on values:

    • Quality

    • Integrity & Trust

    • Drive & Passion

    • Agility & Responsiveness

    • Belonging

    • Collaborative Partnerships