Company:GlaukosIndustry:Medical Technology and PharmaceuticalLevel:Full timeLocation:San Clemente, CACompensation:Base Salary Range: $40,900 - $59,400OVERVIEWPosition SummaryThe Quality Control Inspector II will be responsible for 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.CompensationCompensation for each successful candidate will be based on several factors, which may include qualifications, experience, education, talent availability, and local market conditions. Range listed is not inclusive of additional compensation such as bonus, equity, or additional benefits.›RESPONSIBILITIESQuality AssuranceEnsure all quality records meet good documentation practices in accordance with internal procedures. Coordinate final inspection activities with outside vendors, i,e, LAL, peel testing. Ensures on a daily basis quality records and company practices are compliant with internal procedures and regulations.EngineeringRead engineering drawings and interpret geometric dimensioning and tolerancing. Work with engineering in the design of high quality inspection / metrology fixtures.AnalysisReview associated paperwork, complete inspection records using good documentation practices, and release components. Review device history records for lot release.InspectInspect and release labeling. Inspect finished goods for proper labels, packaging, tamper seals and product in accordance with procedures.ProcessCarefully handle and process extremely small components without damaging them.ProcedureReceiving inspection of components following procedures, specifications and drawings. Write clear and concise procedures for inspection of components, machined tubing, etc. (Level 2 and higher).VisionUtilize 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.ComplianceConduct periodic compliance audits of manufacturing operations and procedures for cGMP compliance.REQUIREMENTSExperienceCollege courses or degree preferred. Level 2: 3-7 years industry experience. 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.SkillsTeam player, good written/oral communicator. Attention to detail and accuracy a must. Must have excellent documentation skills.›ABOUT USFounded in 1998, Glaukos Corporation is an ophthalmic medical technology and pharmaceutical company focused on novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases.Our company was the first company to bring to market Micro-Invasive Glaucoma Surgery (MIGS), the micro-invasive procedure which revolutionized the treatment and management of glaucoma. In 2012, we launched our first MIGS device—the iStent®—in the United States, followed by our next-generation iStent inject® device in September 2018 and iStent inject® W in September 2020.In November 2019, Glaukos acquired Avedro, maker of the first and only FDA-approved cross-linking technology for progressive keratoconus. And we continue to seek to leverage our platform technologies to build a comprehensive and proprietary portfolio of micro-scale surgical and pharmaceutical therapies for glaucoma, corneal health, and retinal diseases.