Hybrid Medical Device System Verification Engineer

Amaris Consulting; Mirandola; Ibrido; EUR 26.000 - 50.000; Tempo pieno

Vantaggi offerti da questo lavoro

Hybrid work model

Internal Academy training

Global exposure

WeCare Together program

Descrizione del lavoro

Amaris Consulting is seeking a System Verification Engineer to join our international team in Mirandola, Italy. You will plan and execute system-level verification for complex medical devices, ensuring compliance with IEC 60601, ISO 13485, ISO 14971 and MDR.

We offer a hybrid work model from Mirandola, with a local salary range and opportunities to grow within a global organisation. You will collaborate with engineering and quality teams and contribute to continuous process improvements.

Competenze

• Plan and execute system-level verification activities for medical devices.
• Develop and maintain verification strategies, protocols, and test cases.
• Ensure compliance with IEC 60601, ISO 13485, ISO 14971, FDA, and MDR.
• Perform requirements traceability and verify/validate system requirements.
• Manage defect identification, reporting and resolution.
• Prepare test documentation including verification plans and reports.
• Support audits and regulatory submissions with verification evidence.
• Contribute to continuous improvement of verification processes.

Mansioni

• Plan and execute verification activities per project requirements.
• Collaborate with cross-functional teams to align objectives.
• Provide verification evidence for audits and submissions.
• Maintain comprehensive test documentation and traceability matrices.

Conoscenze

System verification

Requirements traceability

Test documentation

Regulatory submissions

Analytical skills

Communication skills

English

Italian

Formazione

Engineering

Biomedical engineering

Related field

Strumenti

Traceability tools

Descrizione del lavoro

Amaris Consulting is seeking a System Verification Engineer to join our international team in Mirandola, Italy. You will plan and execute system-level verification for complex medical devices, ensuring compliance with IEC 60601, ISO 13485, ISO 14971 and MDR.

We offer a hybrid work model from Mirandola, with a local salary range and opportunities to grow within a global organisation. You will collaborate with engineering and quality teams and contribute to continuous process improvements.