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10 дней назад

R&D Project Manager (Medtech)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Germany
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
R&D Project Manager (Medtech): Leading regulated medical-device R&D projects from strategy through implementation with an accent on timelines, budgets, risk management, and cross-functional execution. Focus on coordinating multi-site teams, managing product lifecycle requirements, resolving conflicts, and ensuring compliance with ISO 13485 and FDA 21 CFR Part 820.

Location: Hechingen, Baden-Württemberg, Germany; willingness to travel up to 25% required.

Company

Develops vital organ therapy solutions, including dialysis-related digital services and advanced medical technologies, with a focus on improving outcomes for patients and care teams.

What you will do

  • Lead one or more R&D projects, managing timelines, budgets, schedules, execution, and spending.
  • Define program strategies and goals while coordinating core team performance and appraisal activities.
  • Manage product lifecycle requirements to meet customer and business stakeholder expectations.
  • Provide program updates and maintain communication across functions, management levels, and project stakeholders.
  • Identify project risks, develop mitigation plans, and proactively manage risk responses.
  • Resolve conflicts and drive continuous improvement from program identification through implementation.

Requirements

  • Bachelor’s, Master’s, or MBA degree.
  • 10 years of product lifecycle experience and 5 years of project management experience in a highly regulated environment.
  • Demonstrated success leading multi-site projects and cross-functional teams in a matrix organization.
  • Strong expertise in program management, business acumen, communication, stakeholder management, and complex problem-solving.
  • Understanding of medical-device product lifecycle requirements, including ISO 13485 and FDA Quality System Regulation 21 CFR Part 820, is preferred.
  • Willingness to travel up to 25%.

Nice to have

  • PMI/PMP, IPMA, or equivalent project management certification.

Culture & Benefits

  • Work in a fast-paced environment focused on learning and professional growth.
  • Collaborate with teams across functions and management levels.
  • Contribute to medical innovations intended to improve patients’ lives worldwide.
  • Reasonable accommodations are available during the application and interview process.

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