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Strong employer brand and metro location increase applicants, but niche lab-informatics skillset limits competition.
Requires lab informatics and GxP validation experience specific to pharma, limiting industry transferability.
Mandatory 5+ years in regulated pharma plus validation and lab-systems experience makes filters strict.
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Serve as primary liaison between business stakeholders and technical teams to translate laboratory, quality, and operational needs into clear, testable requirements.
Lead requirements lifecycle management including elicitation, documentation (BRDs, user stories, functional specs), test case definition, and traceability through design, testing, and deployment.
Collaborate internationally to deliver integration solutions aligned with business objectives, regulatory expectations, and end-user workflows for digital quality and lab instrument platforms (e.g., Scitara DLX, Empower).
Bachelor’s degree in Engineering, Science, Computer Science, Information Systems, or related discipline.
Minimum 5 years experience as a Business Analyst in regulated environments such as pharmaceutical, life sciences, or manufacturing.
Proven knowledge of SDLC and validation frameworks (GxP, cGMP) and strong understanding of lab operations, quality systems, or laboratory informatics.
Work Experience Required: 5+ years as Business Analyst in regulated domains (pharma/life sciences/manufacturing). Notice period: Not explicitly mentioned in the JD.
Experienced in working with digital quality and lab instrument integration platforms like Scitara DLX, Empower, BIOVIA, MODA, or GLIMS.
Skilled in driving cross-functional collaboration in a global, matrixed environment and capable of independently managing multiple integration or digital workflow initiatives.
Has strong facilitation and stakeholder management skills demonstrated by leading workshops, requirements reviews, and supporting UAT to deliver compliant, user-accepted digital lab transformations.