Project QA Specialist 17690
Veritaz AB
📍 Sverige
⏰ Heltid
📋 Tidsbegränsad anställning
🗓 Ansök senast 10 juni 2026
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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 QA Specialist within project operations for an exciting consulting assignment in the medical device industry based in Uppsala.
What You Will Work On
Participate as the QA representative within projects and ensure quality in project deliveries
Implement and follow up QA activities connected to development and change projects
Ensure compliance with QA processes, policies, and regulatory requirements
Review and approve design documentation such as DHF and technical documentation
Ensure compliance with ISO 13485, MDR, and relevant medical device regulations
Manage and follow up deviations and non-conformities related to projects
Contribute to continuous improvement of quality systems within project environments
Collaborate cross-functionally with project managers, R&D teams, and stakeholders
Support quality assurance activities throughout the project lifecycle
Drive quality-focused initiatives within complex project organizations
What You Bring
Relevant university degree or equivalent professional experience
Approximately 5–8 years of experience within Quality Assurance
Proven experience working with QA activities in project environments
Experience from the medical device industry
Strong knowledge of ISO 13485 and MDR regulations
Documented experience reviewing design documentation such as DHF
Strong understanding of quality systems and industry standards
Ability to work independently and in close collaboration with project teams
Strong communication and stakeholder collaboration skills
Structured and quality-focused working approach
Assignment Description
We are looking for an experienced QA Specialist within project operations for an exciting consulting assignment in the medical device industry based in Uppsala.
What You Will Work On
Participate as the QA representative within projects and ensure quality in project deliveries
Implement and follow up QA activities connected to development and change projects
Ensure compliance with QA processes, policies, and regulatory requirements
Review and approve design documentation such as DHF and technical documentation
Ensure compliance with ISO 13485, MDR, and relevant medical device regulations
Manage and follow up deviations and non-conformities related to projects
Contribute to continuous improvement of quality systems within project environments
Collaborate cross-functionally with project managers, R&D teams, and stakeholders
Support quality assurance activities throughout the project lifecycle
Drive quality-focused initiatives within complex project organizations
What You Bring
Relevant university degree or equivalent professional experience
Approximately 5–8 years of experience within Quality Assurance
Proven experience working with QA activities in project environments
Experience from the medical device industry
Strong knowledge of ISO 13485 and MDR regulations
Documented experience reviewing design documentation such as DHF
Strong understanding of quality systems and industry standards
Ability to work independently and in close collaboration with project teams
Strong communication and stakeholder collaboration skills
Structured and quality-focused working approach