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7 дней назад

Head of Device Product Development (Medical Devices)

82 720 - 113 740€
Формат работы
hybrid
Тип работы
fulltime
Грейд
head
Английский
c1
Страна
Italy
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Текст:
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TL;DR
Head of Device Product Development (Medical Devices): Leading the development, manufacturing, testing, and commercialization of medical devices and drug-device combination products with an accent on design strategy, regulatory compliance, and device quality. Focus on building a device development center of excellence, transferring products to manufacturing, managing multidisciplinary teams and vendors, and applying ISO 13485, ISO 14971, and cGMP frameworks.

Location: Parma, Italy; remote work is possible with regular presence at the R&D Center in Parma

Salary: €82,720–€113,740 annual budgeted salary range for the role based in Italy, plus an annual bonus scheme and benefits.

Company

hirify.global is an international research-focused biopharmaceutical group operating in more than 30 countries, developing and marketing innovative medicines across multiple therapeutic areas.

What you will do

  • Lead and oversee Device Product Development staff and activities for medical devices and drug-device combination products.
  • Define design, development, manufacturing, testing, and product-launch strategies from prototyping through commercialization.
  • Drive innovative device technologies and manage transfers of device products and specifications to manufacturing sites or contract manufacturing organizations.
  • Manage strategic vendors, including design agencies, contract manufacturers, test laboratories, and consultants.
  • Contribute to due diligence, intellectual property strategy, patents, SOPs, project portfolios, and resource planning.
  • Develop the department as a center of excellence while ensuring quality, safety, environmental, cGMP, and regulatory compliance.

Requirements

  • Substantial leadership experience in drug-device combination product development and regulated innovation environments.
  • Experience managing, coaching, and developing multidisciplinary teams through growth, transformation, and delivery.
  • Strategic R&D accountability from concept through commercialization, including industrialization and product optimization.
  • Strong scientific and engineering foundation with extensive hands-on industrial experience.
  • Expertise in medical device quality, risk management, manufacturing, and regulatory frameworks including ISO 13485, ISO 14971, and cGMP.
  • Fluent written and spoken English required.

Culture & Benefits

  • Purpose-driven, sustainable, and ethical working environment as a Benefit Corporation and certified B Corp.
  • Comprehensive pension, private medical insurance, wellbeing, and flexible benefits programs.
  • Flexible working arrangements, remote work options, and tax assistance for foreign colleagues.
  • Professional development through training, resources, and opportunities for growth.
  • Relocation support and performance-based bonus eligibility.

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