Utilize Quality Engineering techniques to ensure compliance with federal, industry, and corporate procedures for calibration
Assist in the implementation of corporate policies and procedures relating to quality, project management, process development, and Quality System Regulation/ISO compliance by reviewing specifications and initiating changes
Plan, prepare, and execute calibrations and analyze data to approve equipment and processes used in testing, processing, storing, and distribution of products
Collect and statistically analyze calibration data
Assist in the development, implementation, and documentation calibration activities to ensure product reliability, safety, and effectiveness prior to release
Requirements
Minimum of a Bachelor’s Degree in engineering field or equivalent experience
Minimum of 1-year hands-on calibration experience; preferably in an FDA regulated industry (i.e., pharmaceutical, biomedical, medical device field)
In-depth knowledge of current Good Manufacturing Practices, Quality System Regulations, and ISO Standards