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Mid-level BA title, metro location, and broad toolset increase applicant density despite niche life-sciences specialization.
Requires deep life-sciences regulatory and operational expertise, limiting cross-industry transferability.
Explicit 4–7 years plus mandatory life-sciences regulatory expertise and technical tooling enforces strict candidate filtering.
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Lead requirements gathering, process mapping, and data analysis for life sciences projects covering R&D, Clinical Trials, Manufacturing, Commercialization, and Regulatory Affairs.
Design and implement technology solutions ensuring compliance with life sciences regulations (FDA, EMA, GxP) that deliver measurable business value.
Mentor junior analysts and act as liaison between business stakeholders, technical teams, and project management to ensure successful project delivery.
Experience: 4 to 7 years in business analysis within life sciences domain.
Strong knowledge of life sciences operations and regulatory compliance including GxP (GLP, GCP, GMP), 21 CFR Part 11, FDA/EMA regulations.
Proficiency in requirements elicitation tools (JIRA, Azure DevOps, Confluence), process modeling (BPMN), advanced SQL, and data visualization (Tableau, Power BI, Qlik Sense).
Work Location: Bangalore
Experienced in multiple life sciences subdomains such as R&D, Clinical Trials, Manufacturing, Regulatory Affairs, Commercial, or Pharmacovigilance.
Capable of bridging complex life sciences operations with technology solutions, including commercial software (LIMS, CTMS, EDMS) and custom development.
Strong stakeholder management including communication of technical concepts to non-technical audiences and coordination of testing (UAT, acceptance criteria).