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
If this sounds interesting please send your CV at cv@veritaz.se
