R&D Engineer

About the role

This is a 6-month onsite contract position in Minnetonka, MN (55345) with possible extension. The schedule is Monday through Friday, 8:00 AM to 5:00 PM.

Responsibilities

• Author and execute Process Validations including Test Method Validation (TMV), Inspection Method Validation (IMV), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Product Performance Qualification (PPQ).
• Lead process development, equipment specification, acquisition, and implementation.
• Apply engineering principles, theories, concepts, practices, and techniques to analyze and solve problems.
• Design and complete experiments, validation, testing, and data analysis for continuous improvement activities.
• Present data to equipment teams and suggest new methods or materials for quality and efficiency improvements.
• Analyze current equipment for process suitability and provide detailed improvement plans.
• Create and revise manufacturing documents, including specifications, SOPs, safety instructions, validation protocols, risk assessments, and technical procedures to ensure compliant, efficient, and safe operations.
• Collaborate with engineers and technicians to develop solutions and improvements in materials, equipment, and processes.
• Participate in teams to drive continual improvement, safety, and compliance.
• Provide training and process expertise in areas such as process development, tooling development, and validation.
• Interact cross-functionally and with internal and external customers.

Requirements

• 1–3 years of experience in a relevant engineering role.
• Bachelor’s degree in engineering or a related field (preferred).
• Experience in the medical device industry.