Job Description

Typically requires a bachelor's degree in mechanical engineering, manufacturing engineering, or related field with a minimum of 0-2 years related experience. Intermediate or advanced beginner with inspection equipment such as: CMM (Mitutoyo Vision and Touch Probe System, OGP vision System, digital microscopes, and others). Intermediate or advanced beginner with engineering software tools for CAD (SolidWorks preferred), engineering analysis, and statistical analysis (e.g. Minitab) Intermediate or advanced beginner with basic statistical analysis (normality, standard deviation, variance, and comparison of data groups) including Gage R&R and test method validation. Intermediate or advanced beginner with geometric dimensioning and tolerancing and the ability to read mechanical drawings is a plus. Proficiency with Microsoft Office Products. Previous direct involvement in the medical device industry or a regulated industry. Ability to run self-directed projects, maintain timelines, transfer technology, and execute projects in an R&D and GMP manufacturing environment. Ability to deal with ambiguity/uncertainty and a willingness to try new/challenging things. Strong interpersonal and teamwork skills. Demonstrated written and verbal communication skills.

Skills Required