At a Glance
- Tasks: Prepare and manage labeling documents while ensuring compliance with regulations.
- Company: CPL Life Sciences, a leader in regulatory affairs.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on process improvements.
- Why this job: Join a dynamic team and make a real impact in the life sciences sector.
- Qualifications: Experience in regulatory affairs and strong attention to detail.
The predicted salary is between 50000 - 65000 £ per year.
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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We think you need these skills to ace Labeling Regulatory Manager – Hybrid On-site 3x/Week in Tadworth
Regulatory Affairs
Labeling Compliance
Document Preparation
Global Regulations Knowledge
Submission Readiness
Process Improvement
Labeling Systems Management
