Coopers Group AG
Systems Engineer Risks and Safety Standards
Skills
2 months ago
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Important information
Contract type:
Permanent
Location:
6343 Risch-Rotkreuz, Switzerland
Work mode:
Onsite
Published on:
21 August 2026
What they need
For Roche Diagnostics, we are looking for an experienced Systems Engineer with a strong background in risk management, safety engineering, and medical device compliance . This role is ideal for professionals with proven experience in regulated product development environments and deep knowledge of critical industry standards such as ISO 14971, IEC 60601-1, IEC 61508, and IEC 62304 .
Hard Facts
- Start Date: 01.10.2026 latest 01.01.2027
- Duration: 12 months
- Extension: Very likely
- Workload: 100%
- Location: Rotkreuz, Switzerland & Mannheim, Germany
- Home Office: Hybrid, minimum 50% onsite presence required
- Travel: Up to 20% to Mannheim, Germany
- Work Model: Hybrid
Responsibilities
- Lead and facilitate Failure Mode and Effects Analysis (FMEA) workshops with cross-functional engineering teams
- Identify hazards and evaluate risks within the product risk management process
- Review and update hardware and software safety and reliability concepts, including functional safety aspects
- Oversee test execution and documentation required for certification board (CB) reports
- Maintain and update technical documentation in accordance with internal and external standards
- Plan, coordinate, and report work packages and project activities to stakeholders
Must-Have Qualifications
- Degree in Electrical Engineering, Mechanical Engineering, Software Engineering, Physics, or a related field
- More than 3 years of experience in product development
- Experience in GMP-regulated environments, including:
- Design Controls
- Good Documentation Practice (GDP)
- Design Transfer
- Risk Management
- Quality Process Compliance
- Fluent English communication skills
Nice-to-Have
- German language skills
Ideal Candidate Profile
The ideal candidate brings hands-on experience across the complete systems engineering lifecycle, including requirements engineering, system architecture, integration, usability engineering, and verification & validation (V&V). A strong track record in medical devices or IVD products, combined with expertise in risk management, safety/reliability engineering, and regulatory compliance, will be key to success in this role.
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