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HomeCompaniesVicentraLead Mechanical Test Engineer

Lead Mechanical Test Engineer

Vicentra · Netherlands, Utrecht, Utrecht · Hybrid · Active · Recruitee

Job facts

FieldValue
CompanyVicentra
TitleLead Mechanical Test Engineer
Normalized title-
Department / teamR&D - Design
LocationUtrecht, Utrecht, Netherlands
Work modelHybrid / Hybrid
Employment typeFull Time
Salary-
Statusactive
ATS providerRecruitee
Posted / first seen2026-04-28 / 2026-05-30
Changed / last seen2026-05-30 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Vicentra.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Recruitee.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Utrecht.Open
Department jobsActive postings in R&D - Design.Open
Work model jobsActive Hybrid postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyVicentra
Sourcefe47ef53-39f3-4fa8-bbed-591437bff668
ATS providerRecruitee

Description

description 🌍 Making Every Move Matter At ViCentra, 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 ViCentra is at a defining moment, scaling across Europe and entering the US market with the Kaleido ecosystem. The devices we build will live on people's bodies, every hour of every day, for years. That's a promise only rigorous testing can keep. As Lead Test Engineer, you are the person who makes that promise real. You will build ViCentra's in-house testing and reliability capability from the ground up, owning the protocols, the rigs, and the evidence base that prove our devices perform, endure, and stay safe long after launch. This is where engineering conviction meets patient trust, and it starts with you. Your impact lies in driving the documentation for test protocols and reports around testing to be of the highest quality. You will define how mechanical, 60601 and EMC testing evidence is generated, documented, and maintained, ensuring that once products are launched, ViCentra has a robust, compliant testing framework it fully owns. Within your first six months, you will establish (FDA‑ready) mechanical test protocols that not only support approval, but also enable ongoing changes, updates, and improvements with confidence. Your work ensures that innovation doesn’t stall after launch, it moves forward safely, compliantly, and at speed. In short, your impact is about taking what has been built and making it future‑proof . Giving teams, regulators, and users confidence that ViCentra’s devices are engineered, tested, and maintained to the highest standards. 🔧 What You’ll Take On You will lead from a technical perspective , with a strong emphasis on documentation, structure, and coordination: Own and author mechanical and EMC test protocols and procedures , written to meet FDA/MDR submission and review standards Coordinate mechanical, software, and EMC testing , including planning, execution oversight, review, and documentation Act as the technical testing authority across R&D, Quality, Regulatory, and external test houses Ensure high‑quality test documentation, reporting, and traceability across projects Balance hands‑on testing with coordination with approximately 80% focus on documentation & project management and 20% hands‑on execution. Support the growth of a Test team , leading through technical expertise. Ensure testing activities align with medical device regulations, relevant standards, and internal quality systems requirements 📌 What You Bring 6+ years of experience in testing, verification, or validation within the medical device industry Proven experience writing mechanical test protocols and procedures for regulatory submissions Strong understanding of FDA expectations and documentation requirements for U.S. market approval Solid background in mechanical testing , with familiarity using basic mechanical test tools Experience coordinating and working with external test laboratories , including EMC testing Comfortable in a role where documentation, planning, and coordination are core responsibilities Technically strong, detail‑oriented, and confident leading from expertise Clear and effective communicator across disciplines 💡 Life at ViCentra Working at ViCentra means joining a team defined by: Courage to create: We experiment, challenge norms, and learn fast. Trust above all: Integrity, honesty, and openness shape our relationships. Customer-first mindset: Every idea is measured by the impact on those we serve. A drive for excellence: We hold ourselves to the highest standard because lives depend on it. Our days move fast, fuelled by curiosity, diverse perspectives, and a love for collaboration. Here, you can shape and be shaped by groundbreaking work in MedTech. 🌱 Grow With Purpose Harness your talent for a mission that truly matters. Enjoy creative freedom, supportive teamwork, and room to lead initiatives. Make a direct impact in people’s lives, today and into the future. Be surrounded by innovators who challenge and cheer you on. 🌏 Every Journey Starts Somewhere — Make Yours Count Here We believe a powerful team is built on unique backgrounds and points of view. If this opportunity excites you but you’re unsure if you fit every bullet, we want to hear your story. At ViCentra, it’s your potential and passion that catch our eye. sharing_description 🌍 Making Every Move MatterAt ViCentra, 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

Full job record

Job ID5b2021701ebffe226546c4e4906fb9479c8c512a
Org ID534eff5a-606e-42f9-867d-7bba39872200
Source IDfe47ef53-39f3-4fa8-bbed-591437bff668
Board IDfe47ef53-39f3-4fa8-bbed-591437bff668
Providerrecruitee
Provider Job Key2583423
TitleLead Mechanical Test Engineer
Normalized Title
Statusactive
Activeyes
Location TextNetherlands, Utrecht, Utrecht
DepartmentR&D - Design
Team
Employment Typefull_time
Workplace Typehybrid
Remote Policyhybrid
CountryNetherlands
RegionUtrecht
CityUtrecht
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://vicentra.recruitee.com/o/lead-mechanical-test-engineer
Apply URLhttps://vicentra.recruitee.com/o/lead-mechanical-test-engineer/c/new
First Seen At2026-05-30 06:11:27Z
Last Seen At2026-06-06 10:23:58Z
Last Checked At2026-06-06 10:23:58Z
Last Changed At2026-05-30 06:11:27Z
Inactive At
Source Posted At2026-04-28 15:23:57Z
Source Updated At2026-05-06 08:18:41Z
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=recruitee/board=vicentra.recruitee.com/date=2026-06-06/2026-06-06T10-23-58-561Z-7850d60d9d4befac92c497b6c6f753f5970bc6c41dc21d7659ec1dd145f5a77f.json
Event Fields
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Parsed Structured
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Extensions
{}
Native Structured
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  "description": "<p class=\"MsoNormal\"><strong>🌍 Making Every Move Matter</strong></p><p class=\"MsoNormal\">At&nbsp;ViCentra, 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.<strong> </strong>We combine technological innovation with human-centered design to empower people with more freedom, confidence, and life on their terms. Our values;&nbsp;Be Bold, Build Trust, Focus on the Customer and Deliver Excellence drive everything we create and every decision we make.</p><p style=\"min-height: 1.7em;\"></p><p class=\"MsoNormal\">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. 🚀</p><p style=\"min-height: 1.7em;\"></p><p class=\"MsoNormal\"><strong>👩💻 Your Impact</strong></p><p class=\"MsoNormal\">ViCentra is at a defining moment, scaling across Europe and entering the US market with the Kaleido ecosystem. The devices we build will live on people's bodies, every hour of every day, for years. That's a promise only rigorous testing can keep.<br><br>As Lead Test Engineer, you are the person who makes that promise real. You will build ViCentra's in-house testing and reliability capability from the ground up, owning the protocols, the rigs, and the evidence base that prove our devices perform, endure, and stay safe long after launch. This is where engineering conviction meets patient trust, and it starts with you.<br><br>Your impact lies in driving the documentation for test protocols and reports around testing to be of the highest quality. You will define how mechanical, 60601 and EMC testing evidence is generated, documented, and maintained, ensuring that once products are launched, ViCentra has a robust, compliant testing framework it fully owns.<br><br>Within your first six months, you will establish (FDA‑ready) mechanical test protocols that not only support approval, but also enable ongoing changes, updates, and improvements with confidence. Your work ensures that innovation doesn’t stall after launch, it moves forward safely, compliantly, and at speed.<br><br>In short, your impact is about <strong>taking what has been built and making it future‑proof</strong>. Giving teams, regulators, and users confidence that ViCentra’s devices are engineered, tested, and maintained to the highest standards.</p><p style=\"min-height: 1.7em;\"></p><p class=\"MsoNormal\"><strong>🔧 What You’ll Take On</strong></p><p class=\"MsoNormal\">You will lead from a <strong>technical perspective</strong>, with a strong emphasis on documentation, structure, and coordination:</p><ul><li><p>Own and author <strong>mechanical and EMC test protocols and procedures</strong>, written to meet FDA/MDR submission and review standards</p></li><li><p>Coordinate <strong>mechanical, software, and EMC testing</strong>, including planning, execution oversight, review, and documentation</p></li><li><p>Act as the technical testing authority across R&amp;D, Quality, Regulatory, and external test houses</p></li><li><p>Ensure high‑quality test documentation, reporting, and traceability across projects</p></li><li><p>Balance hands‑on testing with coordination with approximately <strong>80% focus on documentation &amp; project management</strong> and 20% hands‑on execution.</p></li><li><p>Support the growth of a <strong>Test team</strong>, leading through technical expertise.</p></li><li><p>Ensure testing activities align with medical device regulations, relevant standards, and internal quality systems</p></li></ul><p style=\"min-height: 1.7em;\"></p>",
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  "requirements": "<p class=\"MsoNormal\"><strong>📌 What You Bring</strong></p><ul><li><p class=\"MsoListParagraphCxSpFirst\"><strong>6+ years of experience</strong> in testing, verification, or validation within the <strong>medical device industry</strong></p></li><li><p class=\"MsoListParagraphCxSpMiddle\">Proven experience writing <strong>mechanical test protocols and procedures</strong> for regulatory submissions</p></li><li><p class=\"MsoListParagraphCxSpMiddle\">Strong understanding of <strong>FDA expectations</strong> and documentation requirements for U.S. market approval</p></li><li><p class=\"MsoListParagraphCxSpMiddle\">Solid background in <strong>mechanical testing</strong>, with familiarity using basic mechanical test tools</p></li><li><p class=\"MsoListParagraphCxSpMiddle\">Experience coordinating and working with <strong>external test laboratories</strong>, including EMC testing</p></li><li><p class=\"MsoListParagraphCxSpMiddle\">Comfortable in a role where <strong>documentation, planning, and coordination</strong> are core responsibilities</p></li><li><p class=\"MsoListParagraphCxSpMiddle\">Technically strong, detail‑oriented, and confident leading from expertise</p></li><li><p class=\"MsoListParagraphCxSpLast\">Clear and effective communicator across disciplines</p></li></ul><p class=\"MsoNormal\" style=\"min-height: 1.7em;\"></p><p class=\"MsoNormal\"><strong>💡 Life at ViCentra</strong></p><p class=\"MsoNormal\">Working at ViCentra means joining a team defined by:</p><ul><li><p>Courage to create:&nbsp;We experiment, challenge norms, and learn fast.</p></li><li><p>Trust above all:&nbsp;Integrity, honesty, and openness shape our relationships.</p></li><li><p>Customer-first mindset:&nbsp;Every idea is measured by the impact on those we serve.</p></li><li><p>A drive for excellence:&nbsp;We hold ourselves to the highest standard because lives depend on it.</p></li></ul><p class=\"MsoNormal\">Our days move fast, fuelled by curiosity, diverse perspectives, and a love for collaboration. Here, you can shape and be shaped by groundbreaking work in MedTech.</p><p class=\"MsoNormal\" style=\"min-height: 1.7em;\"></p><p class=\"MsoNormal\"><strong>🌱 Grow With Purpose</strong></p><ul><li><p>Harness your talent for a mission that truly matters.</p></li><li><p>Enjoy creative freedom, supportive teamwork, and room to lead initiatives.</p></li><li><p>Make a direct impact in people’s lives, today and into the future.</p></li><li><p>Be surrounded by innovators who challenge and cheer you on.</p></li></ul><p class=\"MsoNormal\" style=\"min-height: 1.7em;\"></p><p class=\"MsoNormal\"><strong>🌏 Every Journey Starts Somewhere — Make Yours Count Here</strong></p><p class=\"MsoNormal\">We believe a powerful team is built on unique backgrounds and points of view. If this opportunity excites you but you’re unsure if you fit every bullet, we want to hear your story. At ViCentra, it’s your potential and passion that catch our eye.</p><p style=\"min-height: 1.7em;\"></p><p style=\"min-height: 1.7em;\"></p>",
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      "description": "<p class=\"MsoNormal\"><strong>🌍 Making Every Move Matter</strong></p><p class=\"MsoNormal\">At&nbsp;ViCentra, 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.<strong> </strong>We combine technological innovation with human-centered design to empower people with more freedom, confidence, and life on their terms. Our values;&nbsp;Be Bold, Build Trust, Focus on the Customer and Deliver Excellence drive everything we create and every decision we make.</p><p style=\"min-height: 1.7em;\"></p><p class=\"MsoNormal\">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. 🚀</p><p style=\"min-height: 1.7em;\"></p><p class=\"MsoNormal\"><strong>👩💻 Your Impact</strong></p><p class=\"MsoNormal\">ViCentra is at a defining moment, scaling across Europe and entering the US market with the Kaleido ecosystem. The devices we build will live on people's bodies, every hour of every day, for years. That's a promise only rigorous testing can keep.<br><br>As Lead Test Engineer, you are the person who makes that promise real. You will build ViCentra's in-house testing and reliability capability from the ground up, owning the protocols, the rigs, and the evidence base that prove our devices perform, endure, and stay safe long after launch. This is where engineering conviction meets patient trust, and it starts with you.<br><br>Your impact lies in driving the documentation for test protocols and reports around testing to be of the highest quality. You will define how mechanical, 60601 and EMC testing evidence is generated, documented, and maintained, ensuring that once products are launched, ViCentra has a robust, compliant testing framework it fully owns.<br><br>Within your first six months, you will establish (FDA‑ready) mechanical test protocols that not only support approval, but also enable ongoing changes, updates, and improvements with confidence. Your work ensures that innovation doesn’t stall after launch, it moves forward safely, compliantly, and at speed.<br><br>In short, your impact is about <strong>taking what has been built and making it future‑proof</strong>. Giving teams, regulators, and users confidence that ViCentra’s devices are engineered, tested, and maintained to the highest standards.</p><p style=\"min-height: 1.7em;\"></p><p class=\"MsoNormal\"><strong>🔧 What You’ll Take On</strong></p><p class=\"MsoNormal\">You will lead from a <strong>technical perspective</strong>, with a strong emphasis on documentation, structure, and coordination:</p><ul><li><p>Own and author <strong>mechanical and EMC test protocols and procedures</strong>, written to meet FDA/MDR submission and review standards</p></li><li><p>Coordinate <strong>mechanical, software, and EMC testing</strong>, including planning, execution oversight, review, and documentation</p></li><li><p>Act as the technical testing authority across R&amp;D, Quality, Regulatory, and external test houses</p></li><li><p>Ensure high‑quality test documentation, reporting, and traceability across projects</p></li><li><p>Balance hands‑on testing with coordination with approximately <strong>80% focus on documentation &amp; project management</strong> and 20% hands‑on execution.</p></li><li><p>Support the growth of a <strong>Test team</strong>, leading through technical expertise.</p></li><li><p>Ensure testing activities align with medical device regulations, relevant standards, and internal quality systems</p></li></ul><p style=\"min-height: 1.7em;\"></p>",
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