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Job Description
Structured overview of role & requirementsAbout This Role
Translate regulated Pharma/Life Sciences business needs into clear, buildable SAP and digital program requirements across large enterprise transformation initiatives.
Own requirement documentation including BRDs, functional specs, user stories with acceptance criteria, process flows, and traceability matrices for multiple Pharma value-chain domains.
Drive UAT and compliance deliverables under GxP/regulated scope, manage scope changes, support data migration, and contribute to training and hypercare post go-live.
Minimum Requirements
6+ years as a Business Analyst with at least 3 years specifically in Pharma or Life Sciences programs.
Hands-on experience with SAP ECC and/or S/4HANA modules like MM, PP-PI, QM, SD, and EWM.
Strong expertise in requirements engineering and working knowledge of regulated environment standards such as GxP, GMP, 21 CFR Part 11, and computer system validation.
Experience working in both Agile (user stories, backlog grooming) and Waterfall delivery models.
Ideal Candidate Profile
Experienced in multiple Pharma value-chain areas including Manufacturing, Quality Management, Supply Chain, Regulatory, or Commercial domains.
Capable of engaging senior client stakeholders through workshops and able to produce detailed, implementation-ready requirements documentation.
Familiar with compliance-driven environments and able to manage regulatory documentation and validation activities in digital transformation projects.
