Senior MedTech R&D Engineer — V&V & PLM Leader

Grove Technical Resources; Minnesota; On-site; USD 110,000 - 140,000; Full time

Job summary

Grove Technical Resources seeks a Senior R&D Engineer to drive medical device R&D efforts, design controls, and V&V in an integration project. You will transfer specifications, validated test methods, and design documentation into a new PLM and quality system, ensuring regulatory and manufacturing compliance.

The role emphasizes cross-functional collaboration with Quality, Manufacturing, Regulatory, and engineering teams, plus execution of validation activities and documentation control in a

Qualifications

• Bachelor's degree in Mechanical, Biomedical, Electrical Engineering, or a related field with at least 4 years of relevant experience.
• OR Master's degree in a related engineering field with at least 2 years of relevant experience.
• Preferred 5–10 years of R&D Engineering experience, ideally within the medical device industry.
• Strong analytical, problem-solving, communication, and cross-functional collaboration skills.

Responsibilities

• Review and transfer existing engineering specifications into a new Product Lifecycle Management (PLM) system.
• Review and update design inputs and outputs to ensure alignment with product requirements.
• Transfer validated test methods into a new quality system, identify documentation gaps, and update procedures as needed.
• Support test method validation, equipment qualification, and verification and validation activities.
• Review engineering drawings, test protocols, reports, and technical documentation for regulatory and quality compliance.
• Develop, execute, and document verification and validation protocols when required.
• Collaborate with Quality, Manufacturing, Regulatory, and cross-functional engineering teams.
• Support challenge testing, misuse testing, process validation, and Use Failure Mode and Effects Analysis (UFMEA), as needed.
• Ensure all documentation is properly updated and released within electronic document management systems.

Skills

Medical Device R&D Engineering

Medical Device Design Controls

Design Inputs and Outputs

Test Method Validation

Verification & Validation (V&V)

Process Validation

Equipment Qualification

Product Development Process (PDP)

PLM / Document Management Systems

Regulatory and Quality Compliance

Education

Bachelor's degree in Mechanical, Biomedical, Electrical Engineering, or related field

Master's degree in related engineering field

Job description

Grove Technical Resources seeks a Senior R&D Engineer to drive medical device R&D efforts, design controls, and V&V in an integration project. You will transfer specifications, validated test methods, and design documentation into a new PLM and quality system, ensuring regulatory and manufacturing compliance.

The role emphasizes cross-functional collaboration with Quality, Manufacturing, Regulatory, and engineering teams, plus execution of validation activities and documentation control in a