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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.
Reasons to use Rodeo
I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?
Honest answer — it depends on where you want to end up. A lot of top grad schemes (Big 4, civil service, banking) don’t need a masters. Let’s look at the ones you’d be competitive for now, and we can decide if a masters actually adds anything.
Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.
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Graduate Consultant — 2026 Scheme
Why you're a good match
StrongYour economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.
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Why you're a good match
You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.
Experience fit
Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
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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