MVE Biological Solutions is the leading global manufacturer of vacuum insulated products and cryogenic systems. More than 50 years ago, they set the standard for storage of biological materials at low temperatures. Today, they continue to exceed these standards. Industries from around the world look to MVE for excellence and innovation. Their solutions empower industries to better utilize cryogenic technology. In this manner, MVE continues to make a vital contribution in today’s biomedical life sciences industry.

PRIMARY RESPONSIBILITIES (include But Are Not Limited To)

• Partner with the Product Engineering group to ensure that all aspects of new product introduction and changes to existing products are properly communicated to stakeholders, including production personnel
• Conduct validation tests for components, process, and/or products following established protocols
• Conduct routine investigation tests to address engineering, quality and/or manufacturing issues
• Design and draw, in SolidWorks, machine tools and fixtures to be used in the production process
• Assist in routine design updates to legacy product including documentation and data collection
• Conduct and supervise studies to determine the cause, effect, and corrective actions required to remedy product quality deviations
• Partner with production, engineering, and maintenance departments and apply formal problem solving tools (e.g. 5 Why’s, 8D, Ishikawa diagram) to resolve assembly errors and eliminate variances
• Observe and practice safety procedures and policies
• Other duties and responsibilities as assigned by management

COMPETENCIES & PERSONAL ATTRIBUTES

• Passion for, and alignment with, Cryoport’s mission
• An individual who brings strong core values, quality, ethics, and integrity
• A collaborative team player who embraces and champions the culture
• Strong work ethic and ability to deliver results and meet commitments in a dynamic environment
• Demonstrates a business process orientation to developing solutions
• Must possess a working knowledge of computers, including MS Word, Excel, and SolidWorks
• Understanding of MIG/TIG welding practices, sheet metal fabrication, and vacuum systems, a plus
• Familiarity with medical device manufacturing, including working knowledge of industry-specific regulatory policies (e.g. ISO 13485, MDR 2017/745), a plus
• Familiarity with principles of heat transfer, fluid mechanics, and cryogenics, a plus
• Familiarity with Lean and Six Sigma methodologies, and statistical process control, a plus

Qualifications And Education Requirements

Enrollment in a 4-year BS degree program in Engineering, preferably Mechanical, Manufacturing, or Industrial