Relevant third-level qualification in Science, Engineering, IT, or a related discipline preferred.
Demonstrated experience in Computer System Validation (CSV) testing within a pharmaceutical, GMP, or other regulated environment.
Experience in technical writing and documentation within a pharmaceutical, GMP, or regulated environment.
Experience supporting IT compliance, quality systems, or manufacturing/warehouse operations desirable.
Prior exposure to system implementations or digitization projects (e.g., SAP, Tulip, MES, WMS) is highly advantageous.
Strong understanding of controlled documentation, change management, and document management processes.
Strong technical writing and communication skills, with the ability to convert complex or manual processes into clear digital procedures.
Solid working knowledge of CSV testing methodology and documentation (test scripts, protocols, deviation/discrepancy handling).
Excellent attention to detail and commitment to right-first-time documentation and testing.
Ability to interpret operational and technical information and translate it into clear, standardized procedures.
Strong organisational skills with the ability to manage multiple documents, tests, and priorities within a fixed project timeline.
Ability to work independently and collaboratively across cross-functional teams, including warehouse operations staff.
Proactive approach with strong problem-solving skills and comfort working through ambiguity during a transition project.
Strong computer skills and confidence working with document management systems and digital platforms such as SAP and/or Tulip
