Description:

Title:

R D Engineer Duration:

06

Months Location:

Minnetonka, MN ( 55345) Roles and responsibilities Author and execute Process Validations including Test Method Validation (TMV), Inspection Method Validation (IMV), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Product Performance Qualification (PPQ) Responsible for process development, equipment specification, acquisition and implementation. Understands engineering principles theories, concepts, practices and techniques. Analyzes and solves problems from basic engineering principles. Completes design of experiments, validation, completion of testing and analysis of data for continuous improvement activities. Presents data to equipment teams. Suggests and supports new methods or materials for continual improvement of quality and efficiency. Analyzes current equipment for process suitability and provides detailed plans for improvement Creates and revises manufacturing documents, specifications, standard operating procedures (SOPs), safety instructions, validation protocols, risk assessments, and procedures and other technical documents to ensure compliant, efficient and safe procedures. Works with other engineers and technicians in developing solutions and improvements in materials, equipment and process as necessary. Participates in teams as necessary to ensure continual improvement, safety and compliance. Provides training and process expertise for product processing in specific areas such as process development, tooling development and validation. Interacts cross functionally and with internal and external customers.

Preferred education:

Bachelor's degree Required experience: Medical device 1-3 years experience