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Metro location and general QA title increase competition despite niche regulated-software specialization.
Requires pharma GxP/validation knowledge making cross-industry transferability limited.
Explicit 1–3 years requirement plus regulated-software skills and test automation preferences.
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Plan and execute functional testing and system integration of enterprise software platforms used in pharmaceuticals.
Create and manage test cases, metrics, and ensure traceability between requirements and tests in an Agile environment.
Own the quality, reliability, and compliance of product deliverables, including automation of test suites using AI-powered tools.
1 to 3 years experience in enterprise software product development lifecycle.
Strong experience in functional testing including test strategy and test design.
Familiarity with GxP regulations and 21 CFR Part 11 / EU Annex 11 compliance is preferred.
Experience using Jira and Test Management tools like Zephyr or QMS.
Experience or familiarity with pharmaceutical, biotech, or medical devices industries and regulated software.
Ability to work collaboratively and independently with minimal supervision in an Agile team environment.
Experience or knowledge in pharma regulatory, quality, risk, or process validation software systems (e.g., GAMP 5 framework) and AI-powered automation frameworks is a plus.