Position Overview
Summary:
- Supports testing and validation activities for medical devices, ensuring compliance with regulatory and quality standards.
- Ability to interpret engineering drawings and specifications.
Roles & Responsibilities:
- Develop Test Protocols aligned with design verification plans and regulatory requirements.
- Prepare test samples and fixtures for mechanical and functional testing.
- Execute tests and document results per Good Documentation Practices (GDP). Generate Test Reports for inclusion in the Design History File (DHF).
- Coordinate with cross-functional teams to ensure timely completion of testing activities.
Experience Required:
- 2 - 4 years experience.
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