Packaging Coordinator/Regulatory

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£21.1/hour
Posted 1 day ago
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About the role

Packaging Coordinator - England

Contract - PAYE

Location On site - Surrey

Rate: £21.10 per hour


Atrium (EMEA) are supporting a global biopharma company to recruit a detail-driven Packaging Coordinator (Hub Labelling Manager) to join a dynamic and fast-paced regulatory team.

This role plays a key part in preparing, managing, and maintaining product labelling documentation across multiple markets, ensuring compliance with internal standards and global regulatory requirements.

You will act as a subject matter expert (SME) in labelling processes, supporting both operational delivery and continuous improvement initiatives, including digital transformation projects within regulatory affairs.


Key Responsibilities

  • Prepare and maintain regulatory labelling documents (LPDs, LLDs, PLDs) for assigned markets
  • Manage labelling workflows using systems such as GDMS and approved tracking tools
  • Ensure data integrity, perform quality checks, and conduct peer QC reviews
  • Produce submission-ready labelling documentation, including annotated labels and comparison tables
  • Collaborate cross-functionally to gather input and align on regulatory documentation
  • Support regulatory submissions and respond to Health Authority queries and inspections
  • Contribute to process improvements and automation initiatives within labelling operations
  • Participate in digital transformation projects, leveraging tools such as automation and machine learning
  • Assist with regulatory data analysis and enhancement of SharePoint systems

About You

  • Degree in Life Sciences, Pharmacy, or equivalent experience
  • Strong understanding of regulatory labelling principles and compliance requirements
  • Familiarity with structured data systems (e.g., Excel, SharePoint, databases)
  • Confident working across global teams and multiple markets
  • Ability to quickly learn new systems, technologies, and regulatory standards


Skills & Experience

  • Knowledge of global/regional regulatory guidelines and clinical variations
  • Hands-on experience in product registration and labelling lifecycle management
  • Language requirements German and French.


Why Join?

  • Opportunity to work in a highly collaborative, global regulatory environment
  • Involvement in cutting-edge digital transformation initiatives
  • Exposure to complex and innovative product labelling projects


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