Senior Verification & Validation (V&V) Engineer

Senior V&V Engineer – Job Description

Job Details

• Job Title: Senior Verification & Validation (V&V) Engineer

• Industry: Medical Devices

• Work Location: Milpitas, California (Fully Onsite)

• Education Start Date: 26-Oct-2026

• Duration of Assignment: 7 months, with the possibility of extension

• Duration Mentioned: 6 months

• Experience Required: 8–10 years

• Base Salary Range: Minimum and maximum not specified

Educational Qualifications

- Bachelor's or Master's degree in any of the following:

• Biomedical Engineering

• Computer Science / Information Technology

• Electronics Engineering

• Software Engineering

• Life Sciences or a related field

Must-Have Technical/Functional Skills

• Experience in the Medical Device industry.

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

• Hands-on experience with Verification & Validation (V&V) activities.

• Experience with IT systems.

• 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.

• Ability to work independently with minimal supervision.

Preferred Skills

• Familiarity with FDA regulations.

• Knowledge of ISO 13485 standards.

• Familiarity with IEC 62304 standards.

• Experience with medical device quality and regulatory requirements.

Roles and Responsibilities

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

• Prepare validation reports and ensure accurate documentation of results.

• Execute protocols and document observations, deviations, and outcomes.

• Support verification and validation activities throughout the product lifecycle.

• Collaborate with cross-functional teams, including:

  • Engineering

  • Quality

  • Regulatory Affairs

• Work with legacy systems and technologies as required.

• Ensure compliance with applicable quality and regulatory requirements.

• Maintain accurate and complete documentation in a regulated environment.

• Work independently to support V&V activities and project deliverables.

Essential Skills

• Senior Verification & Validation (V&V) Engineering

• Medical Device Industry Experience

• Protocol Development and Execution

• Validation Report Writing

• Verification and Validation (V&V)

• IT Systems

• Legacy Systems and Windows 2000

• Quality and Regulatory Compliance

Desirable Skills

• ISO 13485

• FDA Regulations

• IEC 62304

• Medical Device Quality Systems

Keywords

• Senior V&V Engineer

• Medical Device

• Verification and Validation

• V&V Protocols

• Test Plans

• Protocol Execution

• Validation Reports

• ISO 13485

• FDA Regulations

• IEC 62304

• Legacy Systems

• Windows 2000

• Regulated Environment

• Quality Assurance

• Medical Device Regulations