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Manufacturing Specialist - Injection Moulding

Job in 3500, Utrecht, Utrecht, Netherlands
Listing for: ViCentra B.V.
Contract position
Listed on 2026-09-13
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering, Injection Molding, Lean Manufacturing / Six Sigma
Salary/Wage Range or Industry Benchmark: 70000 - 100000 EUR Yearly EUR 70000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Contract Manufacturing Specialist - Injection Moulding

Join ViCentra – Empower Bold Change in Med Tech

Location:

Utrecht, Netherlands
Hybrid or On-site

Making Every Move Matter

At Vi Centra , we're on a mission to make living with diabetes easier, by designing simple, beautiful, and effective solutions that fit people's lives — not the other way around.

We combine technological innovation with human-centered design to empower people with more freedom, confidence, and life on their terms. Our values;

Be Bold, Build Trust, Focus on the Customer and Deliver Excellence drive everything we create and every decision we make.

We believe that when ambition meets purpose, remarkable things happen. If you thrive in a space where ideas accelerate, challenges spark growth, and making a difference is the goal, ViCentra is your next great adventure.

Your Impact

As Contract Manufacturing Specialist, Injection Moulding, you will help turn ViCentra's ambition to scale into reality on the factory floor. Working hand in hand with our Contract Manufacturing Organisations and critical suppliers, you will be the operational driving force behind the high precision plastic parts that make our wearable insulin devices possible, keeping quality, delivery, capacity, and cost on target every step of the way.

This is a role where hands-on problem solving meets real impact. As we scale production to reach more people living with diabetes, you will be the person who keeps industrialisation projects moving, resolves process issues at the source, and builds the supplier partnerships that make growth dependable. Every improvement you drive brings a life changing device closer to the people who need it.

What

You’ll Take On

In your role, you will:

  • Act as the primary operational point of contact for assigned CMOs and critical injection moulding suppliers on day-to-day manufacturing, assembly, and engineering topics.

  • Support scaling and capacity expansion for injection moulded parts across our contract manufacturers and critical suppliers.

  • Coordinate injection moulding industrialisation projects, driving yield improvement, throughput optimisation, cost reduction, and process stabilisation.

  • Track key injection moulding KPIs such as cycle time, OEE, yield, and scrap, and support root cause analysis and corrective actions with CMO and supplier teams.

  • Facilitate recurring project and performance meetings, tracking priorities and following up on agreed actions and commitments.

  • Support NPI and product change activities for injection moulded parts, coordinating builds, process readiness, and manufacturing feedback.

  • Support verification and validation of injection moulding processes, machines, and equipment (including IQ/OQ/PQ) to meet Medical Device Regulation requirements.

  • Champion continuous improvement between ViCentra and its suppliers using Lean and structured problem solving methodologies.

What You Bring
  • A Bachelor's degree in Mechanical, Manufacturing, Industrial Engineering, or a related engineering discipline.

  • Around 5 years of relevant experience in manufacturing engineering, industrialisation, supply chain engineering, or project-based roles within an outsourced manufacturing environment, ideally with exposure to injection moulding of plastic components.

  • Hands-on experience working with external manufacturers or suppliers producing high volume, high precision plastic components.

  • A solid understanding of injection moulding process troubleshooting and root cause analysis.

  • The ability to manage operational and project activities in parallel in a fast-paced, scaling environment.

  • Strong analytical, problem solving, and structured communication skills, with fluent written and spoken English.

  • Experience in medical devices or other regulated industries (ISO 13485) is a strong plus.

  • Knowledge of Lean and…

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