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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in conducting Pharmacovigilance audits and developing CAPA plans while ensuring compliance with regulatory requirements and Good Pharmacovigilance Practice (GVP). Proven ability to manage projects effectively and provide timely deliverables in a dynamic environment.
Highest-signal resume keywords
Pharmacovigilance AuditsGood Pharmacovigilance Practice (GVP)CAPA Plans DevelopmentPharmacovigilance Legislation KnowledgeProject Management
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Pharmacovigilance AuditsCAPA Plans DevelopmentRegulatory Requirements UnderstandingQuality Assurance ProjectsProject Management
Soft Skills
Problem-SolvingPragmatic Solutions
Industry Keywords
PharmaceuticalBiotechnologyNational Pharmacovigilance LegislationInternational Pharmacovigilance GuidelinesRemote Audits
About the role
Key responsibilities & impact- Plan, prepare, conduct, report, and follow up on various types of Pharmacovigilance audits
- Develop and follow up on CAPA plans
- Execute audits based on comprehensive understanding of regulatory requirements and Good Pharmacovigilance Practice (GVP)
- Perform GVP quality assurance projects for pharmaceutical and biotechnology client companies
Requirements
What you’ll need- Experience in conducting and leading internal and external Pharmacovigilance audits for a variety of stakeholders
- Expert knowledge of national and international Pharmacovigilance legislation and guidelines
- Proficient in managing projects and ensuring deliverables are provided timeously
- Ability to identify issues and offer solutions in a pragmatic way
- Bachelor’s Degree in Life Sciences preferred
- Up to 40% travel
- Ability to conduct remote audits
Benefits
Comp & perks- Freelance position with full-time (1 FTE) or part-time (0.6+ FTE) options
- Remote work in Spain
- Ability to conduct remote audits
- Up to 40% travel
- Supportive, collaborative environment
- Professional growth encouraged
- Opportunity to make an impact across the pharmaceutical and biotechnology industry
- Collaborative team of experts in clinical research, pharmacovigilance, and quality consulting
