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Niche TrackWise specialization reduces applicants, but mid-level Bangalore role increases candidate pool.
Requires TrackWise QMS and regulated medical device process experience, limiting cross-industry transferability.
Multiple mandatory TrackWise, Java, regulatory and industry experience requirements create rigid filtering.
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Own end-to-end TrackWise system analysis including configuration, modification, implementation, and lifecycle management of IT business systems.
Analyze and improve business processes by designing, developing, and deploying TrackWise solutions including workflows, automation, WebServices, and Crystal Reports.
Manage multiple projects by collaborating with onsite, offshore teams, and stakeholders ensuring compliance with regulatory and change control requirements.
4-5 years experience specifically in TrackWise System Analysis.
Experience with TrackWise workflows, business rules, automation, notifications, WebServices development, and Crystal Reports implementation.
Experience in Medical Device manufacturing industry and familiarity with relevant regulations (21 CFR Part 11, GxP, GAMP).
Strong Java programming knowledge and understanding of SDLC processes.
Experienced in gathering business requirements and developing detailed functional design specifications for TrackWise applications.
Capable of independently managing multiple concurrent projects with minimal supervision.
Comfortable working in regulated industries and collaborating across onsite and offshore teams for high-quality solution delivery.