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IT Quality Assurance Manager 18600 Stockholms län, Sweden

Open 35d
This position is no longer accepting applications(closed Aug 16, 2026).

Summary

Manages IT compliance and validation for computerized systems in regulated industries, ensuring adherence to GxP, GMP, and data integrity standards while supporting system lifecycle quality activities.

Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in ensuring the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry.

Assignment Description

We are looking for an experienced Quality Manager IT

What You Will Work On

  • Ensure IT compliance for computerized systems and IT infrastructure
  • Review and approve risk assessments, qualification, and validation documentation
  • Review change controls, deviations, and periodic system reviews
  • Ensure compliance with GMP, GxP, SOPs, and internal quality requirements
  • Support Computerized System Validation (CSV) activities
  • Participate in IT compliance, qualification, and validation projects
  • Provide QA support for IT projects and system changes
  • Ensure data integrity principles are applied across IT systems
  • Maintain and update the inventory of computerized systems
  • Collaborate with QA, IT, Validation, Infrastructure, and Business stakeholders
  • Support continuous improvements in IT quality, security, availability, and compliance
  • Contribute to regulatory inspections and audit readiness
  • Review technical documentation to ensure regulatory compliance
  • Support quality activities throughout the system lifecycle

What You Bring

  • Experience working in IT Compliance within the pharmaceutical, biotech, or other GxP-regulated industries
  • Strong understanding of Computerized System Validation (CSV)
  • Experience reviewing qualification and validation documentation
  • Knowledge of GMP, GxP, and pharmaceutical quality systems
  • Strong understanding of Data Integrity principles (ALCOA+)
  • Experience with change control, risk assessments, and periodic reviews
  • Experience supporting QA and validation activities for computerized systems
  • Excellent communication and stakeholder management skills
  • Pragmatic, solution-oriented, and collaborative mindset
  • Flexible with a proactive approach to quality and compliance


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