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Quality Control Inspector I - 2nd shift
Glaukos San Clemente, CA
$41k-52k (estimate)
Full Time | Medical Technology 8 Months Ago
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Glaukos is Hiring a Quality Control Inspector I - 2nd shift Near San Clemente, CA

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.

Base Salary Range: $35,600 - $51,700

Overview

The Quality Control Inspector 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.

Responsibilities

Receiving Inspection 

  • 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. 
  • Program the Smartscope to run automatic routines for multiple part inspections. (Level 2 and higher) 
  • Write clear and concise procedures for inspection of components, machined tubing, etc. (Level 2 and higher) 
  • Carefully handle and process extremely small components without damaging them. 

In-Process Inspection 

  • Perform Line Clearance for Operations activities 
  • Inspect and release labeling 
  • Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. 
  • Perform inspections on components and assemblies in manufacturing 

Final Inspection 

  • Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. 
  • Perform final inspection on finished goods 
  • Inspect finished goods for proper labels, packaging, tamper seals and product in accordance with procedures. 
  • Coordinate final inspection activities with outside vendors, i,e, LAL, peel testing 
  • Perform in-house peel testing on sealed packages 
  • Maintain sample retain area 

Other Duties 

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

Requirements

Experience

  • College courses or degree preferred
  • Level 1: 1-3 years industry experience 

Knowledge, Skills, and Abilities

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

Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible. 

These are just a few of the terms our employees use to describe their experiences as a part of the Glaukos family.

Those may seem like big aspirations, but 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 eyesight of people worldwide. And because we’re a rapidly growing company with a dynamic, fast-paced culture, individual employees are empowered with more diverse and enriching challenges that might not be possible at a larger company, and more fulfillment in knowing every person and every task is directly tied to making a difference in the life of others.

We offer competitive salary (based on experience), bonus eligibility, medical/dental/vision, life insurance, stock options, 401(k) Employer Match, Employee Stock Purchase Program, generous time off & paid holidays as well as time-off to volunteer in the community, plus the opportunity to work for a company that is pioneering a new glaucoma treatment class! Moreover, Glaukos Corporation has been Certified as a Great Place to Work the last two years!

Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

Job Summary

JOB TYPE

Full Time

INDUSTRY

Medical Technology

SALARY

$41k-52k (estimate)

POST DATE

08/24/2023

EXPIRATION DATE

05/15/2024

WEBSITE

glaukos.com

HEADQUARTERS

SAN CLEMENTE, CA

SIZE

200 - 500

FOUNDED

1998

TYPE

Public

CEO

THOMAS W BURNS

REVENUE

$200M - $500M

INDUSTRY

Medical Technology

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About Glaukos

Glaukos is an ophthalmic medical device firm that creates micro invasive glaucoma surgery options for patients.

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