Quality Engineering Technician-Paso Robles, CA

Trelleborg is a world leader in engineered polymer solutions for almost every industry on the planet. And we are where we are because our talents brought us here. By specializing in the polymer engineering that makes innovation and application possible, Trelleborg works closely with leading industry brands to accelerate their performance, drive their business forward—and along the way, shape the industry and progress that will benefit humankind in the exciting years ahead.

Location

Paso Robles/CA

Trelleborg Healthcare and Medical is headquartered in Paso Robles in an 110,000 square foot state of the art cleanroom manufacturing facility. We are a premier manufacturer for life-saving medical components, and our company is a very dynamic, forward thinking business. We have been active in our lean manufacturing journey for many years and are advancing towards making our business a showcase of excellence in the medical industry. Visit us at www.trelleborg.com

Trelleborg is an ISO 13485 certified manufacturer of custom silicone components and parts for the medical device industry. Our specialties include silicone extrusion, molding, sheeting and closed cell sponge/foam. 

Trelleborg is an Equal Opportunity Employer and offers an excellent benefits package that includes:

  • Life Insurance
  • Medical Insurance
  • Vision Insurance
  • Dental Insurance
  • 401(k) plan
  • Generous PTO plan
  • 11 paid holidays

We currently have an opening for a Quality Engineering Technician. In this role, you will be partnering with Quality Engineers in developing, trouble shooting, standardizing and improving new and existing production methods and procedures for new product release and legacy products. In addition, you will be expected to follow good manufacturing practices (GMP) and principles to help develop and maintain the quality system. 

Some of the essential functions include:

  • Assists Engineers with the tasks related to the development and/or update of Risk Management FMEA and Hazard Analysis documentation 
  • Supports Engineering group in development and performance of operational and process qualifications for customer manufacturing processes 
  • Assists in qualification activities associated with supplier/vendor design characterization requirements for projects, to include audits and assessments 
  • Performs data analysis, researching, compiling and analyzing information and assists in GR&R activities. Creates measurement system programs, when necessary 
  • Communicates quality issues to Quality Engineers  
  • Supports internal and external audit activities 
  • Supports continuous improvement methods to help achieve company goals for a robust and effective system.   
  • Performs product and material testing, as needed. 

Required: 

  • 2 year degree in quality, manufacturing, engineering, or related equivalent experience  

Desired: 

  • 2+ years of regulated manufacturing experience. 
  • Quality certification(s) (e.g. ASQ CQE, CQT, CQA, etc.). 
  • Class I, II and/or III Medical Device manufacturing experience. 
  • Other regulated manufacturing industry experience (e.g. Aerospace, Automotive, Defense, Pharmaceutical, etc.) 
  • Knowledge and experience with GMP/ISO Standards. 

PLEASE NOTE: To be considered, you must apply using this link:   

https://recruiting.ultipro.com/TRE1005TRLB/JobBoard/e29d2cd1-2e41-4fb7-99cf-4974ca632ddb/Opportunity/OpportunityDetail?opportunityId=4bd43c67-3157-4a25-9c84-8257e643bd6f