

Technical Product Lead - Hardware Diagnostics Systems - RZ
Manpower SA
- 15.01.2026
- 21 - 42%
- Fachverantwortung
- Temporär
Technical Product Lead - Hardware Diagnostics Systems - RZ
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The ManpowerGroup is the world's leading provider of workforce solutions.
With our three brands - Manpower, Experis, and Talent Solutions - we support companies in various industries with their recruitment needs. For 75 years, we have been operating in over 75 countries and supporting our clients throughout Switzerland in successfully completing their tasks and projects.
We are looking for a Technical Product Lead - Hardware Diagnostics Systems (m/f/d)
Within an international and highly networked setup, the PCR Hardware Development organisation - including the Instrument Product Care team - is responsible for the long-term maintenance and continuous improvement of complex diagnostic platforms that combine hardware, software and consumables.
In the role of Technical Product Lead (Hardware), you will be an integral part of a cross-functional product team supporting diagnostic instruments used in Nucleic Acid Purification, PCR and Sequencing. Your focus lies on product life cycle activities, technical decision-making and coordination with internal experts as well as external development and engineering partners. You will act as a technical authority, aligning engineering solutions with business and product strategy in close collaboration with Product Management at Roche.
Technical & Project Leadership
Take ownership of the hardware product care scope as technical lead and steer work package planning, execution and prioritisation together with line management
Drive engineering change activities across the product life cycle
Budget, Cost & Progress Control
Manage and control development budgets related to hardware product care and CoGP
Track technical progress and ensure transparency towards key stakeholders
Design Control & Specifications
Define, maintain and approve technical concepts, requirements and specifications
Ensure alignment with internal standards and external development partners
Quality, Reviews & Change Management
Lead and moderate technical reviews and redesign discussions (incl. PCBA and firmware topics)
Approve technical changes and actively contribute to Design Quality Management (DQM) activities
Negotiate technical solutions with business and product representatives
Verification & Risk Management
Oversee planning, execution and documentation of verification activities together with Test Managers and Product Owners
Actively manage technical and project-related risks and contribute to Product Risk Assessments
System Integration & Interfaces
Support system integration and design V&V activities
Resolve interface issues in collaboration with architects and system engineers
Stakeholder & Partner Coordination
Manage external suppliers and engineering partners
Align closely with internal functions such as Business, Operations, Supply Chain and Development
Establish clear and efficient communication structures across Europe, the USA and Asia
Essential Qualifications
Degree in engineering or life sciences (e.g. mechanical or electrical engineering with life science focus) or equivalent professional experience as a Technical Project Leader
At least 3 years of experience in technical project management
Solid knowledge of ISO 13485 and regulated development environments
Proven experience working in a highly regulated industry
Strong motivation and capability to lead technical sub-projects with US-based stakeholders (incl. travel)
Fluency in English (written and spoken); German is a strong advantage
Additional Assets
Background in laboratory diagnostics and/or service & support environments
Experience supporting both hardware and software topics
Familiarity with engineering tools or strong willingness to learn
Personal Attributes
Structured, solution-oriented and proactive working style
Strong communication and negotiation skills
Team-oriented mindset with the ability to work autonomously in complex environments
Start Date: 02.02.2026
Latest Start Date: 01.05.2026
Planned Duration: 12 months
Extension: Very likely, potential internalisation possible
Workload: 100%
Location: Rotkreuz
Home Office: 1 day per week possible
Travel: Approx. 10-20% (Switzerland & USA)
Working Hours: Standard business hours; late meetings with US partners may occur
GxP Environment: Yes
Criminal Record Extract: Required (international travel, incl. USA)
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