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Systems Engineer Risks and Safety Standards

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Systems Engineer Risks and Safety Standards

Coopers Group AG

Systems Engineer Risks and Safety Standards

Skills

ComplianceRegulatory ComplianceRisk Management

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.

Apply now

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