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Senior Hardware & Manufacturing Operations Lead

Оценка ИИ

Отличная вакансия для опытного лидера: работа над социально значимым продуктом, высокая степень ответственности и прямой путь к позиции COO в перспективном стартапе. Единственный минус — отсутствие релокационной поддержки.


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Сложность вакансии

ЛегкоСложно
Оценка ИИ

Высокая сложность обусловлена необходимостью глубоких знаний в области медицинского регулирования (ISO 13485, MDR) и опытом вывода сложных аппаратных продуктов на этап серийного производства. Роль требует сочетания инженерных навыков и операционного управления.

Анализ зарплаты

Медиана95 000 €
Рынок80 000 € – 115 000 €
Оценка ИИ

Зарплата в объявлении не указана, но для позиции уровня Senior Lead в сфере MedTech в Нидерландах рыночный диапазон составляет 80,000 – 110,000 EUR в год. Данная роль предполагает высокую ответственность, что может поднять планку выше среднего.

Сопроводительное письмо

I am writing to express my strong interest in the Senior Hardware & Manufacturing Operations Lead position at MindAffect. With extensive experience in bringing complex medical devices from late-stage R&D into regulated production environments, I am confident in my ability to build the manufacturing foundation for Sofi®. My background in managing external manufacturing partners and ensuring compliance with ISO 13485 aligns perfectly with your current transition phase.

Throughout my career, I have successfully led design transfers, optimized Bills of Materials for scalability, and established robust supply chain operations. I am particularly drawn to MindAffect’s mission of revolutionizing hearing diagnostics through brain-response technology. I am eager to apply my expertise in industrialization and operational execution to help your team deliver high-quality, objective hearing assessments to those who need them most.

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Присоединяйтесь к MindAffect и возглавьте процесс вывода инновационной нейротехнологии на мировой рынок!

Описание вакансии

Senior Hardware & Manufacturing Operations Lead

Practicals

  • Location: Ede, Netherlands (Minimum 1 day per week in office)
  • Employment type: Full-time
  • Travel: Occasional travel to manufacturing partners and suppliers
  • Start date: As soon as possible
  • Applicants must have the legal right to work in the Netherlands. We are not able to provide visa sponsorship for this role.

About MindAffect

MindAffect is a Dutch health-tech company developing the next generation of brain-response-based sensory diagnostics.

Millions of children, elderly people, and individuals with disabilities cannot be reliably tested with today’s hearing assessments, which depend on subjective responses such as pressing a button when a sound is heard. When hearing loss goes undetected, the consequences can include lifelong challenges in language development, cognition, and social interaction.

MindAffect is building a new approach to hearing diagnostics that removes this barrier.

Our technology has received international recognition, including the Innovation Prize at the World Congress of Audiology. We measure how the brain responds to sound, enabling objective hearing assessment without requiring a behavioral response from the patient. At the core of this innovation is Sofi®, a system currently being prepared for regulatory approval that integrates a proprietary EEG headset, a combined EEG/audio amplifier, and our Rapid-CAEP® analysis technology into one platform.The result is a portable and easy-to-use system designed to bring high-quality hearing diagnostics to a much broader range of environments: from hospitals and audiology clinics to retail settings, schools, and community health programs.

MindAffect’s technology is now transitioning from advanced R&D into scalable manufacturing, and we are looking for a Senior Hardware & Manufacturing Operations Lead to help bring our technology into production.

Purpose of the Role

MindAffect is seeking an experienced Senior Hardware & Manufacturing Operations Lead to build and own the manufacturing and operational foundation behind Sofi®.

This is a pivotal role for someone who has experience taking a medical device from late R&D into regulated production environments (ISO 13485) and enjoys bridging engineering, manufacturing, and operational execution.

In the first phase, you will focus on selecting and onboarding the right manufacturing partner and successfully transferring the Sofi design into scalable production.

In the second phase, you will own the operational backbone of the product, including supply chain, production oversight, logistics, and lifecycle support.

As the company grows, this role can naturally evolve into a broader operations leadership position (e.g., Chief Production Officer / COO-type role), becoming the internal authority on everything related to the physical product and its production.

Responsibilities

Phase 1 - Build Manufacturing & Operational Readiness

  • Lead the evaluation, selection, and onboarding of external manufacturing partners
  • Conduct technical, operational, and quality due diligence on potential manufacturing partners
  • Lead the design transfer from the current development partner to the chosen production manufacturer
  • Define the manufacturing strategy and partner responsibilities within CE MDR and FDA frameworks
  • Act as MindAffect’s internal authority on manufacturability, industrialization, and production readiness
  • Translate R&D outputs into production-ready deliverables, including:
  • Bills of Materials (BOMs)
  • Approved supplier lists
  • Assembly instructions
  • Calibration and testing specifications
  • Device Master Record (DMR) documentation
  • Define and implement assembly, verification, calibration, and release processes
  • Establish serialization, traceability, and Device History Record (DHR) processes aligned with ISO 13485
  • Draft and implement Supplier Agreements, Quality Agreements, and operational SOPs
  • Work closely with engineering teams to determine which elements of the design must be optimized for scalable production

Phase 2 - Run Manufacturing, Supply Chain & Operations

Once manufacturing is established, you will oversee the operational lifecycle of the product:

  • Manage day-to-day relationships with manufacturing partners, OEM suppliers, and key vendors
  • Own production planning, purchasing, and supplier performance management
  • Maintain manufacturing documentation, traceability systems, and change-control processes
  • Oversee quality and reliability monitoring for production hardware
  • Design and implement repair, refurbishment, warranty, and RMA processes
  • Establish operational infrastructure for order fulfillment, logistics, and distributor support
  • Support the commercial team with operational execution and product delivery
  • Monitor operational KPIs including cost, reliability, service levels, and warranty exposure
  • Drive continuous improvement across manufacturing quality, scalability, and cost

Requirements

Must Have

  • 5+ years of experience in medical device manufacturing or hardware operations in Europe

Hands-on experience bringing hardware-software medical devices from development into productionProven experience working with external manufacturing partners or OEMs

  • Strong familiarity with ISO 13485 environments
  • Masters degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, Industrial Engineering, or similar
  • Experience establishing manufacturing processes, documentation, and production readiness
  • Understanding of manufacturing  and assembly processes for PCB-based electronics, complex enclosures, connectors, and cables.
  • Ability to work cross-functionally with R&D, regulatory, quality, and external partners

Nice to Have

  • Experience with EEG systems, biosignal devices, sensors, audio electronics, or wearable hardware
  • Knowledge of manufacturing traceability systems, including Device History Records (DHR), serialization, and device tracking
  • Background in early-stage medical device companies transitioning from development to production
  • Exposure to international distribution models, logistics operations, or distributor-based commercialization

Why Join MindAffect

  • Play a central role in transitioning a breakthrough neurotechnology device into global production
  • Take ownership of the entire manufacturing and operational backbone of the company
  • Work with a mission-driven team tackling globally significant healthcare challenges
  • Enjoy a role with real responsibility, visibility, and long-term leadership potential

How to Apply

Send your CV or LinkedIn profile to careers@mindaffect.nl with a brief note describing your experience supporting medical devices into regulated production environments.

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Навыки

  • ISO 13485
  • Medical Devices
  • Manufacturing Operations
  • Supply Chain Management
  • Hardware Engineering
  • PCB Design
  • Industrial Engineering
  • Quality Management Systems
  • CE MDR
  • FDA Regulatory Requirements
  • Bill of Materials (BOM)
  • Design for Manufacturing (DFM)

Возможные вопросы на собеседовании

Проверка опыта работы в строго регулируемой среде медицинских изделий.

Опишите ваш опыт проведения процесса Design Transfer в соответствии со стандартом ISO 13485. С какими основными трудностями вы сталкивались?

Оценка навыков управления внешними подрядчиками, что критично для данной роли.

По каким критериям вы выбираете контрактного производителя (CMO) для сложного медицинского оборудования, сочетающего электронику и механику?

Проверка способности оптимизировать продукт для массового производства.

Приведите пример, когда вам приходилось вносить изменения в дизайн устройства (DFM) для снижения стоимости или повышения надежности при масштабировании.

Оценка понимания жизненного цикла продукта после запуска.

Как бы вы организовали систему отслеживания (traceability) и ведения Device History Records (DHR) для распределенной сети поставок?

Проверка лидерских качеств и видения операционной стратегии.

Как вы видите эволюцию операционных процессов MindAffect при переходе от первой серии устройств к глобальной дистрибуции?

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