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Strong pharma brand, generic Business Analyst title, mid-level (5 years) experience increases competition.
Requires pharmaceutical/life-sciences experience and LIMS/CSV expertise, limiting cross-industry transferability.
Explicit 5+ years, 3+ years specific LIMS/project experience and CSV/GxP mandates make filters strict.
Lead requirements gathering, process modeling, system validation, and deployment for QC laboratory solutions (LIMS, CDS, LabX) ensuring compliance with GxP, CSV, and regulatory standards.
Partner with global Quality Control, Manufacturing, and Technology stakeholders to analyze business processes and define system requirements to support digital quality initiatives.
Drive continuous improvement and adoption of QC technology solutions to enhance operational efficiency and support global quality processes in a regulated pharmaceutical environment.
Minimum 5 years experience in manufacturing, life sciences, pharmaceutical, or process industries with focus on digital technologies and business process improvement.
At least 3 years delivering Quality IT or laboratory systems projects within a regulated pharmaceutical environment.
Proven experience with Quality Control systems such as LIMS, CDS, and LabX.
Strong knowledge of Computerized System Validation (CSV), GxP regulations, and quality management processes.
Experienced in global, matrix organizations with skills to engage senior stakeholders and manage cross-functional collaboration.
Demonstrated expertise in business analysis including requirements gathering, process mapping, and solution design focused on Quality Control and laboratory systems.
Capable of translating complex technical concepts into business language and implementing IT lifecycle management, testing, validation, and change management in regulated environments.