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Strong employer brand and metro mid-level role but niche GxP/LIMS specialization reduces applicant density.
Requires regulated GxP lab and LIMS expertise, so candidates from other industries have limited fit.
Explicit 3-7 years plus mandatory GxP/LIMS and validation experience makes screening highly stringent.
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Elicit, document, and analyze business requirements for lab materials management within a regulated GxP pharmaceutical lab environment.
Support SDLC development and GMP validation of Biovia OneLab platform and related documentation including SOPs, work instructions, and validation records.
Collaborate with cross-functional teams to align system design, conduct gap analysis, assist with UAT, and provide training and support for new systems and processes.
3-7 years of experience as a Business Analyst/Technical Analyst in regulated GxP pharma lab environment.
Experience with Laboratory Information Systems (LIMS/LES), system integrations, and supporting global digital transformation projects.
Technical skills in light coding, database querying (e.g., SQL), system configurations, and familiarity with tools like JIRA, Microsoft Teams.
Location requirement: Based in Hyderabad; Flexible hybrid work arrangement.
Experienced in regulated pharmaceutical labs focusing on materials management and quality control processes.
Proficient in managing regulated documentation and compliance with GxP and data integrity standards.
Skilled at working in global, cross-functional project teams driving digital transformation and system implementations in complex environments.