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Support maintaining validated state of packaging lines (performance checks, lifecycle documentation updates) according to procedures
Support troubleshooting and contribute to systematic problem-solving activities (including LEAN/problem-solving tools) within a defined scope
Support deviations, change control and CAPA activities with a “right-first-time” mindset
Support qualification/validation activities and contribute to documentation suitable for audits
Support implementation and qualification of new equipment to meet growing clinical trial demand
Collaborate cross-functionally with a Design for Manufacturing (DfM) mindset across stakeholders and suppliers
Contribute to continuous improvement (simplify, standardise ways of working, support digitalisation/automation—without compromising quality)
Equipment & Qualification Responsible
Måløv, Capital Region of Denmark, DKPosted 1 weeks ago