At a Glance
- Tasks: Lead global labelling initiatives and ensure compliance across multiple regions and product lines.
- Company: Join a transformative global life sciences organisation making a real impact.
- Benefits: Competitive contract with potential for extension and exposure to a complex operating model.
- Other info: Opportunity to influence senior stakeholders and drive meaningful change.
- Why this job: Take ownership of high-visibility projects that shape the future of labelling in healthcare.
- Qualifications: Experience in labelling, regulatory requirements, and cross-functional collaboration.
The predicted salary is between 60000 - 80000 £ per year.
This is a genuinely high-impact contract sitting within a global life sciences organisation undergoing significant transformation across its Quality and Regulatory landscape. You'll step into a programme-critical role, taking ownership of global labelling initiatives that span multiple regions, product lines, and manufacturing sites. The work is highly visible, strategically important, and sits right at the intersection of Quality, Regulatory, Supply Chain, and commercial delivery.
The role
- You'll act as the central programme lead for labelling across the business.
- Working across Regulatory Affairs, QA, Packaging, Manufacturing, Artwork, and Commercial teams, your focus will be on ensuring labelling is not only compliant, but consistent and scalable globally.
What that looks like in practice:
- Owning end-to-end delivery of global labelling programmes (incl. remediation, harmonisation, and compliance uplift)
- Driving execution of artwork updates, IFUs, UDI implementation, and market-specific labelling requirements
- Leading programme governance - timelines, budgets, risk tracking, stakeholder alignment
- Aligning senior stakeholders across regions to deliver consistent labelling strategies
- Acting as the point of escalation for labelling-related risks, compliance gaps, and operational challenges
- Supporting audit and inspection readiness, particularly around labelling controls and documentation
- Improving how labelling is managed across the business - systems, processes, and ways of working
This is less about 'running projects' and more about bringing order and direction to a complex global programme environment.
What they're looking for
- This role suits someone who sits comfortably between programme leadership, regulatory understanding, and operational delivery.
- You'll likely bring:
- Strong exposure to labelling, artwork life cycle, or product information management
- Solid understanding of global regulatory requirements (FDA, EU MDR/IVDR, GMP, UDI etc.)
- Experience working across multiple functions - particularly Regulatory, QA, and manufacturing
- Confidence influencing senior stakeholders and driving alignment across regions
- Helpful but not essential:
- Experience working with labelling or artwork systems
- Exposure to transformation or large-scale change programmes
What's on offer
- Exposure to a complex, global operating model
- A role with genuine ownership and visibility
- The initial 9-month contract with strong forward planning in place - highly likely to extend into a longer-term programme (~18-24 months).
Next steps
If you're interested, apply now with your latest CV or get in touch directly for more details. If this role isn't right, but you're open to new opportunities in Quality or Regulatory, feel free to reach out for a confidential discussion.
QARA Labelling Contract- MDR IVD- EU US UDI in Basingstoke employer: Hays
Join a leading global life sciences organisation that prioritises employee growth and development within a dynamic and transformative environment. With a strong focus on collaboration across diverse teams, you will have the opportunity to take ownership of impactful labelling initiatives while benefiting from a culture that values innovation and compliance. Enjoy a role that not only offers visibility and strategic importance but also the potential for long-term engagement in a complex global operating model.
StudySmarter Expert Advice🤫
We think this is how you could land QARA Labelling Contract- MDR IVD- EU US UDI in Basingstoke
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those who work in Quality and Regulatory roles. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by researching the company’s recent projects and challenges. This shows you’re genuinely interested and ready to contribute to their labelling initiatives right from the get-go.
✨Tip Number 3
Don’t just wait for job alerts! Actively apply through our website and tailor your application to highlight your experience with global regulatory requirements and stakeholder alignment. It’ll make you stand out!
✨Tip Number 4
Follow up after interviews with a thank-you note. It’s a simple gesture that keeps you on their radar and shows your enthusiasm for the role. Plus, it’s a great way to reiterate your fit for the position!
We think you need these skills to ace QARA Labelling Contract- MDR IVD- EU US UDI in Basingstoke
Some tips for your application 🫡
Tailor Your CV:Make sure your CV speaks directly to the role. Highlight your experience with labelling, regulatory requirements, and any relevant projects you've led. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Share specific examples of how you've tackled similar challenges in the past and how you can bring value to our team.
Showcase Your Stakeholder Management Skills:Since this role involves influencing senior stakeholders, make sure to highlight your experience in this area. We love seeing examples of how you've successfully aligned teams or driven consensus in complex environments.
Apply Through Our Website:We encourage you to apply through our website for the best chance of being noticed. It helps us keep track of applications and ensures you’re considered for this exciting opportunity!
How to prepare for a job interview at Hays
✨Know Your Labelling Regulations
Make sure you brush up on the global regulatory requirements like FDA, EU MDR/IVDR, and UDI. Being able to discuss these confidently will show that you understand the landscape and can navigate the complexities of labelling compliance.
✨Showcase Your Cross-Functional Experience
Prepare examples from your past roles where you've worked across different functions such as Regulatory Affairs, QA, and Manufacturing. Highlighting your ability to collaborate and influence stakeholders will demonstrate that you're the right fit for this programme-critical role.
✨Demonstrate Programme Leadership Skills
Think about times when you've led projects or initiatives, especially in complex environments. Be ready to discuss how you managed timelines, budgets, and stakeholder alignment, as this role requires strong programme governance.
✨Prepare for Scenario-Based Questions
Expect questions that ask how you'd handle specific labelling challenges or compliance gaps. Practising your responses to these scenarios will help you articulate your problem-solving skills and operational delivery capabilities effectively.
