Senior Project Manager Medical Devices

Geistlich; Wolhusen; On-site; CHF 140,000 - 190,000; Full time

Job summary

Geistlich in Root & Wolhusen, Switzerland, seeks a Senior Project Manager Medical Devices to lead complex device development from concept to market readiness. You will coordinate R&D, QA, Regulatory, Operations and Marketing to deliver successful products.

The role requires 8+ years leading multidisciplinary teams and 5+ years in medical devices, with hands-on Design Controls and strong regulatory knowledge (ISO 13485, ISO 14971, FDA/EU MDR).

Qualifications

• 8+ years of experience leading multidisciplinary teams in regulated industries.
• 5+ years of project management experience in Medical Devices, Life Sciences or other highly regulated industries.
• Proven experience leading cross-functional product development projects.
• Hands-on experience with Design Controls from user needs through design transfer.
• Strong knowledge of ISO 13485, ISO 14971, FDA and/or EU MDR requirements.

Responsibilities

• Lead complex medical device development projects from concept through market readiness.
• Own timelines, budgets, resources, risks, deliverables, stakeholder alignment and project reporting.
• Lead cross-functional teams, drive decisions and project governance.
• Ensure compliance with Design Controls and applicable quality/regulatory requirements.
• Coordinate design planning, V&V, risk management, manufacturing transfer and scale up.
• Proactively manage risks, dependencies, and critical issues.

Skills

Leadership

Cross-functional teamwork

Project management

Stakeholder mgmt

German language

English language

Problem solving

Education

Engineering / Biomedical Engineering / Life Sciences degree

Job description

Job ID: 724

Workload: 80-100%

Contract type: Permanent

Location:
Root & Wolhusen (LU), CH

By tradition, we are committed to a pioneering spirit that puts employees at the center. They are committed to what drives Geistlich to excellence: a passion for regeneration. This results in innovative medical products that restore bone, cartilage as well as soft tissue. Our motivated team is looking forward to you and working together in a modern, dynamic working environment with an international flair.

Interesting challenges await us on the way to realizing our vision. For this, we are looking for you as Senior Project Manager Medical Devices.

Shape the future of regenerative medicine

At Geistlich, you will lead complex medical device development projects that contribute to advancing tissue regeneration and improving patient outcomes. From early concept through design transfer and market readiness, you will bring together experts across R&D, Process Development, Quality, Regulatory, Operations, Medical Affairs, and Marketing to turn innovative ideas into successful products.

As Senior Project Manager, you will have the opportunity to shape projects with a high degree of ownership and visibility – working in an international environment where scientific expertise, collaboration, and long-term thinking matter.

Your Responsibilities

• Lead complex medical device development and line extension projects from concept through market readiness
• Own timelines, budgets, resources, risks, deliverables, stakeholder alignment and project reporting
• Lead cross-functional teams, drive decisions and project governance
• Ensure compliance with Design Controls and applicable quality / regulatory requirements
• Coordinate design planning, , V&V, risk management, manufacturing transfer and scale up
• Proactively manage risks, dependencies, and critical issues

Your Profile

• Degree or professional qualification in Engineering, Biomedical Engineering, Life Sciences, Natural Sciences, Pharmacy, or a related field
• 8+ years of experience leading multidisciplinary teams, programs, or complex initiatives in regulated industries
• 5+ years of project management experience in Medical Devices, Life Sciences, IVD or other highly regulated industries
• Proven experience leading cross-functional product development projects
• Hands-on experience with Design Controls from user needs through design transfer
• Strong knowledge of ISO 13485, ISO 14971, FDA and/or EU MDR requirements
• Strong leadership, influencing, and stakeholder management skills, with the ability to lead without direct authority
• Structured, proactive, and solution-oriented approach
• Fluent in German and English
• Experience in biomaterials, regenerative medicine, dental solutions, orthopedics, wound care, diagnostics, biologics, or related healthcare sectors is an advantage

Why Geistlich?

Join a company where science, innovation, and collaboration come together to advance regenerative medicine. At Geistlich, your project leadership will directly contribute to bringing innovative medical solutions from concept to patients.

Work locations: Root and Wolhusen, Switzerland

Does your profile fit our position? Then we look forward to receiving your complete application.