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Specialist, Lab Execution System, Tester
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Drugdiscovery
Hyderabad, India
Hybrid
Gmp validation
Fda 21 cfr part 11
Regulated environment
Skills & Requirements
Must-have
GMP validation
FDA 21 CFR Part 11
regulated environment
test scripts
SDLC development
Nice-to-have
Agile methodologies
LIMS or LES experience
Biovia OneLab experience
Bachelor's degree
Key Requirements
3-7 years in regulated GxP pharma lab environment
Understanding of regulatory requirements
Experience developing test scripts in a regulated environment
Work Rights
Not specified
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