At a Glance
- Tasks: Lead global labelling initiatives and ensure compliance across multiple regions and product lines.
- Company: Global life sciences organisation undergoing significant transformation.
- Benefits: Genuine ownership, visibility, and potential for contract extension.
- Other info: Opportunity to influence senior stakeholders and drive strategic alignment.
- Why this job: Make a real impact in a complex, high-stakes environment.
- 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 Life Sciences
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. This role offers not only visibility and responsibility but also the potential for long-term engagement in a complex global operating model, making it an excellent choice for those seeking meaningful and rewarding employment.
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 diving deep into the company’s values and recent projects. Show them you’re not just another candidate; you’re genuinely interested in their mission and how you can contribute to their labelling initiatives.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation and reiterate your enthusiasm for the role. It keeps you fresh in their minds!
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re proactive and serious about landing that QARA Labelling role.
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 reflects the specific skills and experiences that align with the QARA Labelling role. Highlight your exposure to labelling, regulatory requirements, and any relevant project leadership experience to catch our eye!
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. Mention your understanding of global regulatory requirements and how you can bring order to complex programmes.
Showcase Your Stakeholder Management Skills:Since this role involves influencing senior stakeholders, make sure to include examples of how you've successfully aligned teams in the past. We want to see your ability to drive collaboration across different functions!
Apply Through Our Website:We encourage you to apply directly through our website for the best chance of being noticed. It’s the quickest way for us to get your application and start the conversation about your future with us!
How to prepare for a job interview at Hays Life Sciences
✨Know Your Labelling Inside Out
Make sure you brush up on your knowledge of labelling regulations, especially around FDA and EU MDR/IVDR. Being able to discuss specific compliance requirements and how they impact global labelling initiatives will show that you're not just familiar with the basics, but that you can navigate the complexities of the role.
✨Showcase Your Cross-Functional Experience
Prepare examples from your past roles where you've successfully collaborated with Regulatory, QA, and manufacturing teams. Highlighting your ability to work across multiple functions will demonstrate that you understand the interconnectedness of these areas and can drive alignment effectively.
✨Be Ready to Discuss Stakeholder Management
Think about times when you've influenced senior stakeholders or resolved conflicts. This role requires strong stakeholder alignment, so be prepared to share specific strategies you've used to gain buy-in and ensure everyone is on the same page.
✨Emphasise Your Programme Leadership Skills
Since this position is less about running projects and more about providing direction, come equipped with examples of how you've led complex programmes in the past. Focus on your ability to manage timelines, budgets, and risks while keeping the team aligned and motivated.
