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Salary
≈ $43k – $87k per year (Estimated)
Location
In office (Eindhoven)
Seniority
Middle · 3+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 21, 2026. First seen by Alion on Aug 13, 2026.

Overview
Company
Impact
Profile match
Xeltis is an international medical technology company developing vascular and valve implants that transform into living blood vessels through the body's own tissue formation. Its aXess vascular access implant is CE marked, and its vacancies include sales, cleanroom, manufacturing, supply chain and research and development roles. The company is headquartered in Eindhoven, Netherlands.

The opportunity

This is a build role, not a maintenance role. You will own supply chain end-to-end for our implantable devices at the moment it matters most: the transition from clinical supply to commercial launch. There is no established team to inherit and no legacy machine to keep running. You will design the demand, procurement, inventory and logistics processes a compliant, resilient medical device supply chain depends on, run them hands-on, and recruit and lead the team around you as commercial volume grows. You will work daily with Quality, Regulatory, Manufacturing, Finance and Commercial, and report into operations leadership.

What you'll own

  • End-to-end supply chain: demand planning, procurement, inventory, logistics and S&OP for implantable devices.
  • The monthly S&OP cadence, driven with Sales, Operations, Finance and Manufacturing, and the forecast accuracy behind it.
  • Sourcing and supplier strategy for raw materials, implant components and packaging: negotiation, performance management, and (with Supplier Quality and Regulatory) qualification and audits.
  • Inventory health: service levels, turns, traceability and obsolescence risk, under full lot traceability.
  • Domestic and international logistics, warehousing and distribution, with a constant eye on cost and service.
  • Supply chain readiness for new product introductions, from material planning to launch.
  • Supply risk and continuity: mitigation, contingency and business-continuity planning across suppliers, capacity and materials.
  • Building the function: as volume scales, recruiting and leading planners, buyers and logistics, and setting the standard for how the team operates.

Compliance is the baseline

Everything above runs inside a regulated quality system. You will keep supply chain activities compliant with EU MDR, ISO 13485 and GMP, maintain full product traceability, and support internal, supplier and regulatory audits. FDA 21 CFR 820 / QMSR experience is a plus as we scale internationally.

Is this you?

This role is for you if:

A blank page energises you. You want to build, not maintain.

You're comfortable owning outcomes before you have a team to delegate to.

You can hold service, cost, compliance and continuity in your head at the same time.

You want the scope of a leadership role now, not in five years.

It's probably not for you if:

- You want a mature ERP, settled processes and a team already in place.

- You prefer deep specialisation in one lane over end-to-end ownership.

What you'll bring

  • 3-5+ years in supply chain, spanning planning, procurement and inventory.
  • Either first-line management experience, or clear readiness and appetite to step into your first management role and build a team.
  • Working knowledge of demand planning, inventory optimisation, strategic sourcing and S&OP.
  • Hands-on ERP experience.
  • A Bachelor's or Master's in Supply Chain, Operations, Business or a related field.
  • Fluent English; German, Dutch or Spanish is a plus.

Nice to have

  • Experience in medical devices, implants, pharma or another regulated life-sciences environment.
  • APICS/ASCM CSCP or CPIM, or Lean Six Sigma (Green or Black Belt).
  • Experience managing 3PLs and FDA-regulated manufacturing.

How you'll be measured

Simple and outcome-based: OTIF ≥ 98%, forecast accuracy ≥ 85%, healthy inventory turns and low backorders, strong supplier on-time delivery and quality, and clean audit and traceability compliance.

About Xeltis

Xeltis is a cardiovascular medical technology company developing a new class of restorative implants: devices engineered to be gradually replaced by the patient's own living tissue. Our lead product, aXess, is a restorative vascular access conduit for patients on haemodialysis. Following CE marking, we are moving into commercial launch. We are around 60 people, headquartered at the High Tech Campus in Eindhoven, and building the functions that will carry our technology to patients at scale.

What we offer

  • The ownership of building a function end-to-end, with the scope and visibility of being early.
  • Direct impact on getting a genuinely novel technology to patients who need it.
  • A growing, international team of around 60 people who take the science seriously, move fast, and are easy to work with
  • Real ownership, fast decisions, and the chance to see your work reach the clinic
  • A culture built on five values we actually use: innovate, listen, grow, act, and joy

Apply

This is a full-time, on-site role in Eindhoven, the Netherlands. Ready to help patients heal with their own living tissue, and to help us bring it to market? Apply below.

Questions first? Reach out to Felix Bindels, HR Business Partner, at [email protected].

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