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Tier-1 brand and metro Hyderabad increase interest, but senior GxP specialization reduces broad applicant density.
Strong regulated GxP, clinical systems validation, and QE leadership requirements limit cross-industry transferability.
Explicit 10+ years, leadership requirement, and many mandatory QA/GxP technical skills create stringent shortlisting filters.
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Lead establishment and governance of Quality Engineering CoP and practices across R&D IT globally, focusing on automation and regulatory compliance for GxP systems.
Develop and oversee scalable, automated testing frameworks and strategies (UI, API, Data/ETL, Performance) integrated into CI/CD pipelines with regulatory adherence (FDA 21 CFR Part 11).
Collaborate cross-functionally with stakeholders and teams to align quality strategies, drive Agile integration, and lead recruitment and talent development for QE teams in India.
Bachelor’s degree in IT, computer science, life sciences, or related field; advanced degree preferred.
10+ years in Software Quality Engineering or related fields with at least 3-5 years in leadership/management.
3+ years technical experience in programming languages (Java, JavaScript, Python, Groovy) and automation frameworks (e.g., Selenium).
Work Experience Required: 10+ years in QE or related, with leadership experience; notice period: Not explicitly mentioned in the JD.
Experienced leader with proven ability to build and scale QE teams in India from scratch within a global biopharma IT environment.
Strong technical expertise and hands-on experience in automation frameworks and quality engineering leadership, especially within GxP-regulated contexts.
Strategic collaborator able to align QE initiatives with regulatory requirements, Agile delivery, and cross-functional global teams.