Labeling Regulatory Manager – Hybrid On-site 3x/Week

CPL Life Sciences is seeking a Regulatory Affairs professional focused on labeling to join our team in Tadworth. The role requires preparing labeling documents, ensuring compliance with global and local regulations, and supporting submission readiness in a hybrid work model (3 days on site).

You will work with Regulatory, Medical, and R&D to drive process improvements, manage labeling systems, and respond to HA inspections, maintaining high attention to detail and pace.

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