Back to Job SearchROLE OVERVIEW
We are currently seeking a V&V Engineer to join a leading player in the Pharmaceutical and Medical Device industries, supporting their innovative projects across various locations globally. This is an excellent opportunity for a motivated professional to contribute to critical verification and validation activities within a company known for its continuous growth and commitment to excellence. The role is remote, offering flexibility to candidates across the US looking to make an impactful contribution in a regulated environment.
As the V&V Engineer, you will be pivotal in ensuring products meet all functional, performance, and regulatory standards, working closely with cross-disciplinary teams to uphold quality and compliance throughout product development. Your expertise will support both ongoing and upcoming projects, shaping the success of cutting-edge medical technologies and medicines in dynamic markets.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the V&V Engineer will be varied however the key duties and responsibilities are as follows:
• Plan, execute, and document verification and validation (V&V) activities to ensure products meet functional, performance, and regulatory requirements.
• Apply human factors engineering principles to product development and lead usability studies and assessments as part of V&V activities.
• Develop and execute test protocols and test plans, including in vitro and in vivo testing, and analyze results to support product validation.
• Maintain traceability between user needs, design inputs, and validation activities throughout the product development lifecycle.
• As the V&V Engineer, you will ensure compliance with industry standards and regulatory expectations, contributing to successful product launches and sustained quality.
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the V&V Engineer we are looking to identify the following on your profile and past history:
• A Degree or higher level in a related field (e.g., Biomedical Engineering / Quality Assurance / Regulatory Affairs).
• Proven industry experience in Verification & Validation engineering within a regulated industry, preferably medical devices or pharmaceuticals.
• A working knowledge and practical experience with FDA regulatory requirements, including V&V documentation expectations under 21 CFR Part 820.
WHAT’S IN IT FOR YOU?
Joining our client as a V&V Engineer provides an exciting career opportunity in a global leader supporting groundbreaking medical and pharmaceutical innovations. You’ll benefit from a dynamic, remote working environment and the chance to shape products that impact lives worldwide. This role offers excellent professional development prospects within a company committed to scientific excellence and industry leadership.
Key Words: V&V Engineer / Verification and Validation / Medical Device / Pharmaceutical / Human Factors Engineering / Usability Studies / FDA / 21 CFR Part 820 / Product Development / Remote / Regulated Industry
"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career".
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
