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12 часов назад

Project Manager (f/m/d) (Medical Devices)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
c1
Страна
Germany
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Project Manager (f/m/d) (Medical Devices): Leading multiple prototype development projects and production launches using APQP project management practices, with an accent on cross-functional leadership, regulatory documentation, and manufacturing cost calculations. Focus on coordinating flawless launches, improving product development KPIs, managing make-or-buy decisions, and supporting medical device requirements including FDA regulations.

Location: Würselen, Germany

Company

Medical technology company developing prototypes and launching regulated medical device products into production.

What you will do

  • Lead multiple prototype development projects and new production launches using APQP project management practices.
  • Coordinate cross-functional teams to deliver projects on time and ensure flawless production launches using ARAS and IPQC best practices.
  • Maintain project documentation in line with regulations, procedures, customer requirements, and notified body requirements.
  • Measure, report, and continuously improve product development and launch KPIs.
  • Support design, cost, pricing, and quotation standards, including manufacturing cost calculations and new work center costs.
  • Review and direct make-or-buy decisions while maintaining company, safety, ergonomic, and housekeeping standards.

Requirements

  • Degree in natural sciences, biomedical engineering, or a comparable field.
  • At least five years of professional project management experience.
  • Excellent German and English skills, written and spoken.
  • Strong leadership, communication, assertiveness, structured problem-solving, responsibility, and customer focus.
  • Proficiency with project management tools such as MS Project, JIRA, or Confluence.

Nice to have

  • Project management certification such as PMI or IPMA.
  • Initial experience with medical device regulatory requirements, especially FDA regulations.

Culture & Benefits

  • Full-time employment.
  • Commitment to equal opportunity, diversity, and inclusion.
  • Work focused on regulated medical device development and production launches.

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