At a Glance
- Tasks: Manage and maintain product labelling documentation while ensuring compliance with global regulations.
- Company: Join a leading global biopharma company with a dynamic regulatory team.
- Benefits: Competitive pay, collaborative environment, and opportunities for professional growth.
- Other info: Work with global teams and gain exposure to complex labelling projects.
- Why this job: Be part of innovative projects and contribute to digital transformation in the biopharma industry.
- Qualifications: Degree in Life Sciences or Pharmacy, with knowledge of regulatory labelling principles.
The predicted salary is between 21.1 - 21.1 £ 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
- 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
- Knowledge of global/regional regulatory guidelines and clinical variations
- Hands-on experience in product registration and labelling lifecycle management
- Language requirements: German and French
- 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
Packaging Coordinator/Regulatory in England employer: Atrium
Atrium is an excellent employer that fosters a collaborative and innovative work culture, making it an ideal place for a Global Labelling Specialist. Employees benefit from ongoing professional development opportunities and the chance to work on cutting-edge labelling projects in the UK, ensuring both personal growth and meaningful contributions to the industry. With a focus on compliance and teamwork, Atrium provides a supportive environment where your expertise in regulatory labelling can truly shine.
