X4 Life Sciences
Compliance Specialist

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About the Role
Our client is looking for a consultant to help build and implement a practical PPWR and EUDR compliance program. The consultant will organize the work, define required documentation, support supplier data collection, and help establish repeatable processes for ongoing compliance. This will be a 4 month initial contract that can be completed on a fully remote basis.
Key Aims
The key aims of the project are to ensure the following:
- Producing a clear PPWR and EUDR program structure with assigned owners and priorities
- Assuring that a supplier data and documentation collection process is in place
- Core templates, trackers, and records organized for audit and customer-response readiness
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.
Key Responsibilities
- Create a simple program plan for PPWR and EUDR implementation
- Define roles, responsibilities, milestones, and escalation points
- Identify required supplier data and documentation
- Collect the data from the suppliers and create required documentation or databases for storage
- Develop supplier request templates, questionnaires, and tracking tools
- Support review of supplier responses and identify gaps
- Create templates for declarations, due diligence records, and packaging compliance documentation
- Create a controlled repository for evidence and customer responses
- Prepare concise status updates, risk summaries, and leadership reports
- Develop SOPs for new processes
- Train internal teams on the new process and hand off a sustainable operating model


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Requirements
- Experience with EU regulatory, sustainability, packaging, supplier, or quality compliance programs.
- Ability to convert regulatory requirements into workable business processes.
- Packaging engineering background or similar to work with suppliers
- Experience with supplier documentation, declarations, technical files, or due diligence records.
- PPWR & EUDR
- Medical device, manufacturing, or regulated-product experience
This is a great opportunity for someone who wants to take ownership of a high-impact regulatory compliance program.
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