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Validation and Verification Engineer

Job in 8011 AA, Zwolle, Overijssel, Netherlands
Listing for: EPM Scientific
Full Time position
Listed on 2026-05-14
Job specializations:
  • Engineering
    Biomedical Engineer, Quality Engineering, Validation Engineer, Medical Device Industry
Salary/Wage Range or Industry Benchmark: 60000 - 80000 EUR Yearly EUR 60000.00 80000.00 YEAR
Job Description & How to Apply Below
We are seeking a  Verification & Validation (V&V) Engineer  to ensure compliance and process integrity for medical devices involving neutron activation technologies. This role focuses on validating complex processes within a regulated environment, ensuring adherence to international standards and supporting product performance requirements. You will work closely with specialised nuclear facilities and multidisciplinary teams to ensure robust and efficient activation processes.

Location
Overijssel, Netherlands (Hybrid)

Start Date
ASAP

Key Responsibilities

Verification & Validation:  Develop, execute, and maintain V&V plans, Validation Master Plans (VMPs), protocols, and reports for neutron activation processes. Ensure full traceability and compliance with ISO 13485, ISO 14971, FDA 21 CFR Part 820, and radiological safety guidelines.

Process Compliance & Optimisation:  Validate and optimise neutron activation processes in collaboration with specialised nuclear research reactors and irradiation facilities. Identify and implement CAPAs to improve efficiency and minimise risks.

Regulatory Coordination:  Collaborate with QA/RA teams to meet all regulatory verification and validation requirements and close Change Control Processes (CCP).

Design Validation:  Participate in verification and design validation activities for device components, ensuring performance requirements and user needs are met.

Documentation & Reporting:  Prepare comprehensive reports and present findings to internal stakeholders and external regulatory bodies.

Qualifications

Bachelor's or Master's degree in Engineering (Mechanical, Nuclear, Biomedical, or related field).

Proven experience in V&V within medical device development.

Strong understanding of regulatory standards: ISO 13485, ISO 14971, FDA 21 CFR Part 820.

Familiarity with radiological safety guidelines and reactor-based processes.

Excellent documentation and compliance skills.

Preferred Experience

Hands-on experience with process validation and change control in a regulated environment.

Knowledge of neutron activation technologies and associated safety standards.

Experience managing CAPAs and risk mitigation strategies.

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