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Metro location and generalist BA title increase competition, but LIMS/regulatory specialization and vendor focus moderate it.
Strong LIMS, lab workflow and medical-device compliance requirements limit cross-industry transferability.
Mandatory 1–5 years LIMS experience plus regulatory validation, vendor coordination, and procurement makes shortlisting strict.
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Collaborate with site SMEs, IT Project Manager, and vendors to support and enhance laboratory IT systems including LABVANTAGE LIMS, Waters Empower, and Veeva.
Coordinate project activities including requirements gathering, design reviews, UAT, vendor management, and procurement related to laboratory systems.
Ensure compliance with Medical Device regulations and support system validation and documentation to meet 21 CFR Part 11 and ISO 13485 standards.
1-5 years of experience as a Business Analyst supporting LIMS or laboratory systems.
Hands-on experience with LABVANTAGE LIMS, Waters Empower, and/or Veeva.
Experience working in a Medical Devices regulated environment with knowledge of system validation and compliance.
Work hours from 1 PM to 10 PM IST; Bachelor's degree in Life Sciences, Engineering, IT, or related field preferred but not explicitly mandatory.
Experienced in coordinating cross-functional teams including technical and non-technical stakeholders and external vendors in a regulated Medical Device environment.
Capable of translating complex laboratory and AI-driven business needs into actionable system requirements with attention to quality and compliance standards.
Proficient in handling procurement processes, vendor negotiations, and maintaining documentation for audits and system validation.