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Pv Auditor

2+ years
Not Disclosed
10 April 24, 2025
Job Description
Job Type: Full Time Education: B.Sc. 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: PV Auditor
Location: Remote
Employment Type: Full-time
Department: PV QA


About the Company:

PrimeVigilance, a part of the Ergomed Group, is a specialized mid-size pharmacovigilance service provider founded in 2008. With global organic growth, PrimeVigilance’s teams are based across Europe, North America, and Asia. We provide services in Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance, supporting pharmaceutical and biotechnology partners globally. We prioritize employee well-being, mental health, and work-life balance, contributing to a high-quality client service environment.


Job Responsibilities:

  • Manage and conduct internal and external audits to ensure compliance with PrimeVigilance and/or Client’s procedures, regulatory requirements, and contractual agreements.

  • Conduct audits based on the agreed Audit Plan, including pre-audit activities management.

  • Audit types include:

    • Audits of PrimeVigilance’s Partners and Vendors/Service Providers

    • Internal Audits of Projects and Processes

  • Document audit findings, identify process improvement initiatives, and compile them in an Audit Report within agreed formats and timelines.

  • Serve as Co-Auditor for full Vendor and Internal System Audits or Lead for Full PV Vendor Audits.


Required Qualifications:

  • B.Sc. in Science, Nursing, or a related scientific field

  • Sufficient experience in pharmaceutical/biotech pharmacovigilance, with knowledge of GVP-related Quality Management and Assurance, and GxP auditing experience in an Audit Lead role

  • In-depth knowledge of applicable GxP regulations (e.g., EU and FDA regulations, particularly EU GVP)

  • Strong analytical, written, and oral communication skills

  • Ability to manage tasks, deliver expected outcomes in an organized manner, and communicate changes proactively

  • Strategic thinker with a risk-based, proactive approach to problem-solving

  • Strong team player

  • Proficient in English (written and spoken); additional languages are a plus

  • Proficiency in MS Office applications (Word, Excel, PowerPoint)

  • Knowledge of EDMS (e.g., Veeva Vault, Master Control, Trackwise) is a plus


What We Offer:

  • Training and career development opportunities

  • Focus on personal and professional growth

  • Friendly and supportive work environment

  • Opportunity to collaborate with colleagues globally, using English as the common language


Core Values:

  • Quality

  • Integrity & Trust

  • Drive & Passion

  • Agility & Responsiveness

  • Belonging

  • Collaborative Partnerships