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Orion

PV Coordinator, PV System Management and Agreements

Orion

. Coordinate and support PV audits and inspections, including documentation request management and data room support .

Posted 11/9/2026full-timeEspoo • FinlandJuniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in pharmacovigilance operations, including audit coordination, regulatory compliance, and process improvement. Proficient in managing information-sharing platforms and supporting training initiatives within a collaborative environment.

Highest-signal resume keywords
Pharmacovigilance ExperienceGxP Compliance KnowledgeAdvanced IT SkillsSharePoint ManagementProcess Improvement

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
PharmacovigilanceRegulatory ComplianceAudit CoordinationData ManagementProcess Development
Soft Skills
CollaborationTime ManagementDecision-MakingCommunicationProactive Approach
Tools & Technologies
MS OfficeSharePointAdobeCopilot
Industry Keywords
PharmacyLife SciencesGVPCAPAPSMF

About the role

Key responsibilities & impact
  • Coordinate and support PV audits and inspections, including documentation request management and data room support
  • Coordinate responses to GVP audit questionnaires
  • Maintain eLearning modules and access control for external users
  • Support GVP training plan metrics
  • Manage SharePoint and other information-sharing platforms with service providers, including access control and SOP/WI sharing
  • Provide PV Agreements and communication support for PV Managers
  • Manage simple PV-related agreements, including CDAs, market research agreements and agreement amendments
  • Manage GVP deviations and CAPAs with service providers and subsidiaries
  • Support PSMF and regional annex maintenance activities
  • Collaborate broadly with global and local pharmacovigilance teams and other stakeholders
  • Develop processes and ways of working and contribute to digital transformation in pharmacovigilance operations

Requirements

What you’ll need
  • Suitable background, such as B.Sc. or M.Sc. in Pharmacy, Life Sciences, information technology or a related field
  • Some previous experience in pharmacovigilance, regulatory or GxP-related tasks
  • Advanced IT skills, including MS Office, SharePoint, Adobe and Copilot
  • Fluency in English, the working language
  • Basic spoken Finnish is considered an advantage
  • Collaborative and proactive approach
  • Good time and task management skills
  • Good decision-making and prioritization skills
  • Strong commitment and motivation for continuous process improvement
  • Good communication and interpersonal skills
  • Ability to work effectively across functions and cultures
  • Can-do attitude and openness to continuous learning

Benefits

Comp & perks
  • Opportunities to influence global pharmacovigilance operations and processes
  • Meaningful responsibility and opportunities to contribute to process development
  • Opportunities to develop new ways of working and digital transformation
  • Opportunity to deepen expertise and broaden capabilities in international pharmacovigilance operations and digital transformation
  • Professional and collaborative working environment
  • Career paths and development opportunities
  • Friendly, respectful, appreciative and diverse culture
  • Approved medical examination and drug testing prior to employment
  • Security clearance prior to employment