What are the responsibilities and job description for the Calibration Technician position at Artivion, Inc.?
Position Overview
Utilizes Quality Engineering techniques to ensure that Artivion complies with all applicable federal, industry, and corporate procedures, guidelines, and regulations for calibration during the receipt, use, storage, manufacture, and distribution of products.
Responsibilities
Utilizes Quality Engineering techniques to ensure that Artivion complies with all applicable federal, industry, and corporate procedures, guidelines, and regulations for calibration during the receipt, use, storage, manufacture, and distribution of products.
Responsibilities
- Assist in the implementation of corporate policies and procedures relating to quality, project management, process development, and Quality System Regulation/ISO compliance by periodically reviewing specifications for functionality and initiating the required changes, establishing procedures and integrated program plans for achieving reliability in accordance with specifications and procedures.
- Assists engineers in formulating test, calibration, repair, and evaluation plans and procedures to maintain precision accuracy of measuring, recording, and indicating instruments and equipment.
- Plan, prepare, and execute calibrations on less complex equipment and analyze data to approve equipment and processes used in the testing, processing, storing, and distribution of products.
- Collect calibration data in support of statistical analyses.
- Assist in the development, implementation, and documentation calibration activities to ensure that the products processed are proven to be reliable, safe, and effective prior to release.
- Effectively complete “other” functions that may be assigned.
- Bachelor’s Degree in science field or equivalent work experience.
- 1 year experience in any of the following: equipment management, calibration, electronic systems and/or electronic control devices.
- 1 year experience in a regulated industry (i.e., pharmaceutical, biomedical, medical device field or related field) with knowledge of current Good Manufacturing Practices, Quality System Regulations, and ISO Standards.