Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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У роли четко описана ответственность за полный цикл запуска продукта и взаимодействие между командами, а связь с генетикой и лечением бесплодия делает ее задачи и цель понятными.
Четкие задачи
Медицина и генетика
Международный масштаб
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
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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