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Label Manager

Tadworth
Posted 8 days ago
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Label Manager

Hub Labelling Manager

Location: Walton Oaks, Surrey (Hybrid) Contract: 12 Months Hours: 37 hours per week Languages: English (essential); French and German (preferred)


About the Role

We are seeking an experienced Hub Labelling Manager to join our global regulatory affairs team, supporting pharmaceutical products across multiple international markets.

Key components of the role:

  • Responsible for preparing, maintaining, and managing local and global labelling documentation
  • Ensuring compliance with regulatory requirements, internal SOPs, and global standards
  • Acts as a subject matter expert on labelling activities, supporting regulatory submissions, process improvements, and digital transformation initiatives
  • Works collaboratively with cross-functional stakeholders across global markets

Key Responsibilities

  • Develop, maintain, and update Local Product Documents (LPDs), Local Label Documents (LLDs), and Product Label Documents (PLDs) in compliance with regulations and SOPs.
  • Prepare supporting labelling documentation, including:
    • Annotated labels
    • Comparison tables
    • Track-change versions
    • Submission-ready materials
  • Ensure document integrity and compliance across document management and workflow systems.
  • Conduct quality control reviews of labelling documentation produced by team members.
  • Assist with regulatory submissions and respond to regulatory authority queries.
  • Support readability testing and compliance documentation related to labelling.
  • Drive continuous improvement initiatives, identifying efficiency opportunities in labelling processes.
  • Support digital transformation projects, including:
    • Automation
    • Machine learning
    • Data management
    • Process optimisation
  • Contribute to labelling data analysis and development of SharePoint sites/digital solutions.
  • Collaborate with cross-functional teams to ensure high-quality, compliant, and timely labelling deliverables.

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Skills & Experience

Essential

  • Degree in Life Sciences, Pharmacy, or related field OR equivalent industry experience.
  • Fluency in English; French and/or German a plus.
  • Regulatory Affairs, Labelling, or pharmaceutical compliance experience.
  • Deep understanding of label compliance and regulatory guidelines (local, regional, and global).
  • Experience preparing and maintaining regulatory labelling documentation.
  • Proficiency with MS Excel, databases, and document management systems (e.g., SharePoint).
  • Strong analytical, problem-solving, and attention-to-detail skills.
  • Excellent written and verbal communication for global team collaboration.
  • Ability to manage multiple priorities and deliver in a fast-paced, collaborative environment.

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Desirable

  • Exposure to product registration lifecycle management and commercialization processes.
  • Knowledge of Core Data Sheets (CDS) and their link to local labelling requirements.
  • Understanding of pre-approval and post-approval labelling processes.
  • Experience with process automation, machine-learning-driven compliance, or digital transformation projects.
  • Familiarity with regulatory inspections and Health Authority interactions.

What We’re Looking For

The ideal candidate delivers: ✅ Highly organised, detail-oriented approach to regulatory excellence ✅ Strong regulatory expertise with a collaborative mindset ✅ Keen interest in improving processes through technology and automation ✅ Ability to work elegantly in a global, evolving regulatory landscape ✅ Proactive problem-solving rooted in strict standards and efficiency

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Skills

Regulatory Affairs
Labelling
Documentation Management
Quality Control
Analytical Skills
Problem-Solving
Attention to Detail
Communication Skills
Collaboration
Digital Transformation
Process Improvement
Data Management
MS Excel
SharePoint
Pharmaceutical Industry
Lifecycle Management

Location

Tadworth, England, United Kingdom

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