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Senior Project Manager

Adaptive Business Group

Mainz

Vor Ort

EUR 80.000 - 120.000

Vollzeit

Vor 30 Tagen

Zusammenfassung

A leading company in medical technology seeks a senior project manager to drive R&D projects from concept to market. This impactful role involves leading multidisciplinary teams, ensuring compliance with regulations, and managing project risks to enhance patients' lives through innovative medical device solutions.

Leistungen

Flexible working hours with partial remote options
Tailored onboarding and professional development
Modern office spaces and free parking
Regular team events

Qualifikationen

  • 8–10 years of experience managing complex projects in regulated industries.
  • Strong understanding of medical device standards (MDR, ISO 13485).
  • Experience with agile or hybrid project management approaches preferred.

Aufgaben

  • Lead cross-functional teams to deliver medical device solutions.
  • Develop project plans, timelines, and budgets.
  • Ensure compliance with regulatory requirements and quality standards.

Kenntnisse

Risk Management
Problem Solving
Project Management
Interdisciplinary Team Leadership
Communication (English & German)

Ausbildung

Master’s degree in Engineering, Medical Technology, or related field

Tools

Project Management Tools
Digital Collaboration Platforms

Jobbeschreibung

Are you ready to drive complex, high-impact medical device R&D projects from idea to market?

Join an innovative company at the forefront of medical technology and lead multidisciplinary teams to bring life-enhancing products to patients worldwide.

Your Key Responsibilities:

  • Lead cross-functional teams to deliver new medical device solutions from concept through design transfer and launch.
  • Develop detailed project plans, timelines, budgets, and resource allocations to ensure on-time, on-budget delivery.
  • Ensure that all project phases comply with applicable regulatory requirements and internal quality management standards.
  • Coordinate with internal departments, global partners, and external collaborators, including design houses and manufacturing vendors.
  • Identify potential project risks early, propose mitigation strategies, and drive solutions proactively.
  • Organize and facilitate project meetings, workshops, and milestone reviews for stakeholders at all levels.
  • Act as the central point of contact for project status updates and ensure transparent communication with management and stakeholders.
  • Foster a collaborative team culture, promote knowledge sharing, and encourage continuous improvement within project teams.

Your Profile:

  • Master’s degree in Engineering, Medical Technology, Biotechnology, or a related scientific field.
  • Minimum of 8–10 years’ experience managing complex projects in a regulated industry — ideally in medical devices, diagnostics, or pharmaceuticals.
  • Solid understanding of medical device standards and regulations (e.g., MDR, ISO 13485, ISO 14971, FDA QSR).
  • Proven track record of successfully leading interdisciplinary development teams and external partners.
  • Strong risk management and problem-solving skills.
  • Experience with project management tools and digital collaboration platforms.
  • Familiarity with agile or hybrid project management approaches is a plus.
  • Excellent communication skills in English & German.
  • Motivated, structured, and solution-oriented mindset with a passion for improving patients’ lives.

The Offer:

  • An impactful role in a company dedicated to medical innovation.
  • A supportive, collaborative work environment with flat hierarchies.
  • Tailored onboarding and professional development opportunities.
  • Flexible working hours with the option for partial remote work.
  • Competitive salary package and additional benefits.
  • Modern office spaces, free parking, and regular team events.

Ready to take the next step?

Apply today or reach out to Hollie Dear at Adaptive Life Science for a confidential conversation.

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