Position Overview

Inspector I Job Description
Performs and documents QC inspection activities to assure conformance to specification and procedural requirements.
Provides feedback to QA, Operations and R&D on quality issues.
Initiates non-conformance reports.
Performs special projects as directed.

Inspector II Job Description
QC Inspector II is proficient in performing all duties and responsibilities of QC Inspector I and assists the QC Lead in reviewing of device history record to assure compliance. Assists the Receiving Inspection Supervisor in the preparation of pre- and post- sterilization and of the release of product to Finished Goods. • Performs and documents QC inspection activities to assure conformance to specification and procedural requirements • Provides feedback to QA, Operations and R&D on quality issues • Initiates non-conformance reports • Assists QC Lead in reviewing and closing Build Records • Assists Receiving Inspection Supervisor in the preparation of product for pre-sterilization and in inspection of product post-sterilization • Performs special projects as directed
  • Inspector I, Quality Control
    • High School diploma or equivalent.
    • Minimum 1 year of experience in medical device manufacturing.
    • Demonstrated knowledge of inspection techniques, understanding and reading technical documentation including mechanical drawings.
    • Working in controlled environments (clean rooms).
    • Detail-oriented.
    • Good interpersonal skills.
    • Knowledge of GMP (QSR) and/or ISO regulations.
    • Ability to work in a fast-paced environment and to balance and prioritize workload to support production schedule.
    • Good written and verbal communication skills.
    • Some knowledge of computer software, including Microsoft Word and Excel.

    Inspector II, Quality Control
    • Demonstrated knowledge of inspection techniques; understanding and reading technical documentation including mechanical drawings • Good written and oral communication skills • Working in controlled environments (clean rooms) • Detail-oriented • Good interpersonal skills • Knowledge of GMP (QSR) and/or ISO regulations • Knowledge of computer software, including Microsoft Word and Excel • Ability to work in a fast-paced environment and to balance and prioritize workload to support production schedule • Ability to balance and prioritize to support production • Minimum 3 years experience in medical device manufacturing • Previous experience with video inspection equipment and other inspection tools desirable • Previous experience working with microscopes • High School diploma or equivalent • Good reading and written communication skills