Please strictly adhere to the following resume naming convention:
Must Have TechnicalFunctional 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
Role Descriptions: Key ResponsibilitiesDevelop, 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.
Essential Skills: Senior V&V Engineer
Desirable Skills:
Keyword:
Skills: ISO 13485EIS : Medical Device & Regulations
Experience Required: 8-10
