Copy - Quality Control Inspector

Introduction
Here at Glaukos, we recognize the deep significance and profound meaning that comes from knowing that we can make a meaningful difference by helping improve the eyesight of people worldwide. Because we’re a rapidly growing company with a dynamic, fast-paced culture, employees here are empowered with more diverse and enriching challenges than might not be possible at a larger company.
Overview
Based in San Clemente, the responsibilities of the Quality Control Inspector will include all aspects of inspection (receiving, in-process and final). In addition, this position will provide QSR support for other QA activities such as calibration, environmental monitoring, product testing, label control, etc.
Responsibilities

• Receiving inspection of components following procedures, specifications and drawings.
• Utilize a variety of standard metrology equipment, including: Optical comparator, height gauge, master height gauge, CMM, Vision Metrology System (VMS, e.g., Smartscope), calipers, micrometers, surface table, gauge blocks, pin gauges, dial indicators, durometer, measuring microscope, hardness testers, pull force testers, surface roughness testers, etc.
• Read engineering drawings and interpret geometric dimensioning and tolerancing.
• Review associated paperwork, complete inspection records using good documentation practices, and release components.
• Carefully handle and process extremely small components without damaging them.

In-Process Inspection

• Coordinate the monthly environmental monitoring of the cleanrooms.
• Work with engineering in the design of high quality inspection / metrology fixtures.
• Ensures on a daily basis quality records and company practices are compliant with internal procedures and regulations.
• Support equipment and process validation activities by inspecting process outputs.
• Coordinate quarterly dose audits.
• Conduct periodic compliance audits of manufacturing operations and procedures for cGMP compliance.

Requirements
Education:

• 1-3 years industry experience.

Responsibilities

• Team player, good written/oral communicator.
• Must be organized and able to coordinate activities with outside vendors.
• Experience working in a clean room and/or performing in-process assembly and manufacturing verification inspections desirable.
• Medical device experience and working knowledge of QSR a must.
• Attention to detail and accuracy a must.
• Must have excellent documentation skills.

Glaukos compensation ranges were not directly given to LinkedIn and are estimated ranges from similar roles outside of Glaukos. Glaukos provides competitive industry and functional compensation. Please apply and inquire with your recruiter.