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Job Description
Structured overview of role & requirementsAbout This Role
Own the development, implementation, and continuous improvement of global Quality Control systems within a GxP environment.
Translate global stakeholder business requirements into scalable digital QC solutions and ensure compliance.
Support rollout, validation (CSV), and change management for Quality Control technologies across Technical Operations.
Minimum Requirements
Minimum 5 years' experience in manufacturing, process, or pharmaceutical industries with exposure to digital technologies and global business environments.
At least 3 years' experience delivering Quality IT projects and managing system implementations in regulated (GxP) environments.
Proven experience with Computerized System Validation (CSV) and Quality Control systems like LIMS, CDS, LabX, or similar.
Bachelor's degree in Computer Science, IT, MIS, or related discipline.
Ideal Candidate Profile
Experienced in bridging business and technology for QC systems in global pharmaceutical or manufacturing settings.
Demonstrated capability in requirements gathering, process mapping, stakeholder management, and solution design for regulated environments.
Comfortable owning system lifecycle activities including validation, testing, rollout, and change management in GxP-compliant organizations.