Process Development Engineer — Medical Device (Onsite — Maple Grove, MN) Co at Pharmavise Corporation

Maple Grove, Minnesota, United States -

Full Time

Start Date

Immediate

Expiry Date

06 Mar, 26

Salary

0.0

Posted On

06 Dec, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Process Development, Product Development, Engineering Documentation, Quality Compliance, Testing Processes, Tooling Design, Cross-Functional Collaboration, Technical Development Process, Product Development Process, Data Analysis, Specification Writing, Training, Equipment Validation, Research Data Compilation, Improvement Identification

Industry

Business Consulting and Services

Description

Our F500 Medical Device client has an exciting opportunity for a Process Development Engineer. Job Summary: Assists in the development and analysis of products, materials, processes, or equipment. Under direct supervision/guidance, compiles, analyzes and reports operational, test, and research data to establish performance standards for newly designed or modified products, processes, or materials. Responsibilities: Undertakes and successfully completes simple or basic project/product development tasks to include any of the following: writing and/or verifying specifications, maintaining product/process documentation, testing processes, equipment, raw materials and product, and validating equipment and processes. May assist in inventing / creating concepts and designs/approaches for new products/processes/test methods. Designs, procures, and fabricates simple tooling and fixtures. Designs and coordinates rudimentary engineering tests and experiments. Applies the Technical Development Process (TDP)/Product Development Process (PDP) methodologies. Prepares standard reports/documentation to communicate results to technical community. Completes basic tasks on engineering documentation. Train technicians/operators on new processes and/or test procedures. Identifies areas for improvement, suggests solutions, and submits idea records. Quality Systems Duties and Responsibilities: Build Quality into all aspects of their work by maintaining compliance to all quality requirements. Qualifications 0 - 1 Year with BS Bachelors of Science/Biomedical/Mechanical Chemical or Material Science preferred Additional Job Specific Requirements: Collaborates effectively with cross functional peers. Other Details: Schedule: 08:00:AM - 04:30:PM Contract Length: 12 months Work Set-Up: Onsite in Maple Grove, MN Start Date: 12/29/2025

Responsibilities

The Process Development Engineer will assist in the development and analysis of products, materials, and processes. Responsibilities include completing project development tasks, maintaining documentation, and training technicians on new processes.