Negotiable
Undetermined
Undetermined
Manchester, England, United Kingdom
Summary: The role of a Quality Assurance Analyst at a leading healthcare technology company involves ensuring the highest standards of quality, compliance, and reliability in healthcare technology solutions. The candidate will design and execute test plans, validate regulatory compliance, and collaborate with cross-functional teams to enhance patient outcomes. A strong background in QA methodologies and healthcare or biological sciences is essential for success in this position. This role offers the opportunity to contribute significantly to the development of innovative healthcare products.
Key Responsibilities:
- Design and execute comprehensive test plans for healthcare software applications and medical devices
- Validate that systems meet all regulatory requirements including HIPAA, FDA, and other relevant healthcare standards
- Create and maintain detailed test documentation including test cases, protocols, and reports
- Perform risk assessments and develop mitigation strategies for identified quality issues
- Collaborate with cross-functional teams including developers, data scientists, and clinical specialists
- Verify the accuracy and integrity of biological data processing systems
- Conduct user acceptance testing to ensure solutions meet healthcare provider and patient needs
- Monitor and report on quality metrics throughout the product lifecycle
- Participate in product release decisions based on quality assessments
Key Skills:
- Bachelor's degree in Computer Science, Biological Sciences, Biomedical Engineering, or related field
- 3+ years of experience in quality assurance, preferably in healthcare or life sciences
- Understanding of healthcare regulations and compliance requirements (HIPAA, FDA, etc.)
- Experience with QA methodologies, tools, and best practices
- Knowledge of biological data systems, healthcare workflows, or medical devices
- Strong analytical and problem-solving abilities
- Excellent communication skills, both written and verbal
- Attention to detail and commitment to quality excellence
- Experience with automated testing frameworks and tools
- Knowledge of GxP, 21 CFR Part 11, or ISO 13485 standards
- Background in clinical data validation or laboratory testing environments
- Familiarity with electronic health record (EHR) systems
- Experience with Agile development methodologies
- Understanding of bioinformatics or genomic data processing
Salary (Rate): undetermined
City: Manchester
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: IT