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4 дня назад

Project Manager New Product Introduction (Genetics)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
Spain
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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TL;DR
Project Manager New Product Introduction (Genetics) (Life Sciences/Medtech): Leading end-to-end genetics product introduction projects from concept and development through validation, regulatory submission, and commercial launch with an accent on cross-functional governance, regulated product development, and budget control. Focus on coordinating multinational teams, applying stage-gate methodologies, managing senior stakeholders, and connecting technical and business decisions.

Location: Valencia, Spain

Company

hirify.global provides medical devices and genetic services for fertility treatment, serving customers in more than 110 countries through its own presence and distributor network.

What you will do

  • Own the full lifecycle of genetics new product introduction projects from concept and design through development, validation, regulatory submission, and commercial launch.
  • Lead cross-functional, multi-site project teams across R&D, Market Access, Quality, Operations, Product Management, Marketing, and other stakeholders.
  • Manage senior stakeholders and sponsors through structured governance, transparent status reporting, risk management, and decision tracking.
  • Apply stage-gate methodologies and design review processes to align technical and business decisions.
  • Ensure delivery on time, within scope and budget, including resource and expenditure tracking.

Requirements

  • BSc and MSc in Life Sciences, Biomedical Engineering, Pharmacy, Biotechnology, or a closely related field.
  • 4–6 years of hands-on clinical or innovation project management experience within a global life sciences, IVD, medtech, or biotech organisation.
  • Experience owning the full project lifecycle from early-stage innovation through technical development, regulatory submission, and market introduction.
  • Track record of senior stakeholder and sponsor-level management in complex, matrixed organisations.
  • Experience in IVD/MDR-regulated development environments, including MDR/IVDR, FDA 510(k), De Novo, CLSI guidelines, and LDTs.
  • Budget accountability and experience tracking status, resources, and expenditure in PPM tools and Power BI.
  • Experience applying stage-gated product development and market introduction processes, including design reviews and cross-functional milestone governance.
  • Multi-site and multinational project coordination experience, strong project governance and risk management skills, and proficiency with project portfolio management and collaboration platforms.
  • Excellent English communication skills. Background in diagnostics, medtech, or life sciences and a good understanding of genetics and/or laboratory services.

Nice to have

  • Additional management or business education, such as an MBA or equivalent.
  • PMP and/or PRINCE2 certification.

Culture & Benefits

  • Work within the Strategy & Sustainability area and multinational, cross-functional teams.
  • Values include integrity, quality, innovation, and collaboration.
  • Full-time position based in Valencia.
  • Work on products and services aimed at improving fertility treatment outcomes.

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