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Strong employer brand and metro location, but niche GxP systems skills limit applicant pool.
Requires regulated GxP, CSV, and quality-systems experience specific to pharma/FMCG manufacturing.
Explicit 3+ years plus mandatory eQMS/LIMS/SAP/CSV and regulated compliance requirements increase filter rigidity.
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Lead implementation and enhancement of digital Quality Assurance systems (eQMS, LIMS, MES, TrackWise, Veeva) to improve compliance and operational efficiency.
Ensure data integrity and regulatory compliance (USFDA, MHRA, EU GMP), including conducting audits and risk assessments.
Drive digital transformation and process automation in quality operations, including system validation, data analytics, and document management.
BSc/MSc Science Graduate.
Minimum 3 years of experience in healthcare/FMCG industry within manufacturing, quality, or technical operations.
Experience with digital quality systems such as eQMS, LIMS, SAP, Proficy; strong understanding of Computer System Validation (CSV/CSA).
Familiarity with ALCOA+ data integrity principles and regulatory requirements (USFDA, MHRA, EU GMP).
Experienced in managing cross-functional digital QA system projects involving IT and quality teams.
Strong analytical skills with ability to utilize data analytics and BI tools for quality improvement and predictive decision-making.
Comfortable handling validation documentation, maintaining audit readiness, and managing team responsibilities in QA digital transformation contexts.