IT Quality Assurance Engineer with the pharmaceutical, medical device, biotech or life-science industry experience
Location: Remote/Hybrid (Poland)
Employment type: Full-time, employment contract
Key Responsibilities
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Collaborate with Business Analysts, Software Developers, and End Users to understand system functionality and verify that solutions meet specifications.
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Develop detailed test scripts and test cases.
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Perform software validation activities and ensure compliance with regulatory standards (e.g., FDA).
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Develop, implement, and maintain test procedures, testing tools, and test environments.
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Log and track software defects using the client’s defect-tracking systems.
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Contribute to test strategy planning to improve efficiency and shorten testing cycles.
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Perform computer systems validation (CSV) across multiple platforms and technologies.
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Provide ongoing software quality assurance support to the client’s IT Department.
Required Skills & Qualifications
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MUST HAVE - Experience in the pharmaceutical, medical device, biotech, or life-science industry/projects.
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Minimum 2 years of commercial experience.
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Formal qualifications or certifications in Software Quality Assurance (ISEB / ISTQB).
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Strong knowledge of FDA/ISO standards and regulatory requirements.
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Understanding of GAMP5, QSR 820.70i, 21 CFR Part 11.
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Familiarity with test automation tools and frameworks.
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Knowledge of programming and scripting.
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Working knowledge of Microsoft .NET, Java J2EE, HTML.
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Fluent English.