Digital Quality Systems Specialist

ARTO

LeinsterFull-timeMid LevelOn-site

Job Description

We are seeking an experienced Quality Systems professional to support the management and continuous improvement of global electronic Quality Management Systems (eQMS) within a regulated environment. This role focuses on system administration, configuration, validation support, troubleshooting, and driving process improvements while collaborating with international cross‑functional teams to ensure compliance and operational efficiency.

Key Responsibilities

  • Administer and support global eQMS platforms, ensuring compliance and system effectiveness
  • Manage user access, licences, and system permissions across multiple sites
  • Coordinate with local administrators to maintain alignment between global and site‑level processes
  • Monitor system performance, resolve technical issues, and manage support requests efficiently
  • Assist with system configuration, upgrades, enhancements, and implementation activities
  • Support validation activities, including documentation review and protocol execution
  • Maintain training materials, SOPs, and system‑related documentation
  • Ensure compliance with GxP requirements, data integrity standards, and quality processes
  • Contribute to digital quality initiatives aimed at improving workflows and operational efficiency
  • Identify system improvement opportunities and support continuous improvement activities
  • Collaborate with Quality, IT, and cross‑functional teams to ensure process consistency
  • Assist with internal and external audits, inspections, and compliance activities

Candidate Profile

  • Degree in a scientific, IT, engineering, or related discipline
  • 4+ years’ experience in pharmaceutical, life sciences, or other regulated industries
  • 3+ years hands‑on experience with Quality Management Systems or regulated digital platforms

Required Skills & Experience

  • Strong knowledge of eQMS administration and support
  • Experience working in GxP environments with understanding of EU, FDA, and ICH requirements
  • Skills in system configuration, troubleshooting, and end‑user support
  • Knowledge of Computer System Validation (CSV) and validation lifecycle activities
  • Ability to work across global and local teams in a multi‑site environment
  • Strong analytical, organisational, and problem‑solving abilities with high attention to detail
  • Strong communication skills with experience delivering training and user support
  • Effective cross‑functional collaborator in multinational environments
  • Fluent English (written and spoken)
  • Familiarity with GAMP guidelines and digital transformation initiatives
  • Experience with system implementations, upgrades, or optimisation projects
  • Exposure to ISO standards and regulated documentation frameworks
  • Experience in global or multi‑site organisations

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Posted 2 months ago

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