Senior Medical Device Verification & Validation (V&V) Engineer

Must Have Technical/Functional Skills

· Medical Device industry experience.

· Strong experience in protocol writing, execution, and report generation.

· Hands-on experience in Verification & Validation (V&V) activities.

· IT systems experience.

· Exposure to legacy operating systems, particularly Windows 2000.

· Ability to work with legacy technologies and systems.

· Knowledge of regulated environments and quality processes.

· Strong analytical and problem-solving skills.

· Excellent written and verbal communication skills.

· Self-motivated and able to work with minimal supervision.

· Familiarity with FDA, ISO 13485, and IEC 62304 standards is a plus.

Roles & Responsibilities

We are looking for a senior-level Verification & Validation (V&V) Engineer with experience in the Medical

Device industry. The ideal candidate will be responsible for protocol development, execution, and

reporting while working independently in a regulated environment.


Key Responsibilities

· Develop, review, and execute V&V protocols and test plans.

· Prepare validation reports and ensure accurate documentation of results.

· Perform protocol execution and document observations, deviations, and outcomes.

· Support verification and validation activities throughout the product lifecycle.

· Collaborate with cross-functional teams including Engineering, Quality, and Regulatory Affairs.

· Work with legacy systems and technologies as required.

· Ensure compliance with applicable quality and regulatory requirements