QA Engineer II - Up to $20K Sign-on Bonus! Job at RCI for Confidential Companies (hosted jobs)

RCI for Confidential Companies (hosted jobs) Santa Cruz, CA 95060

QA Engineer II

Santa Cruz, CA and Morgan Hill, CA

How does joining a growing team of medical device professionals sound to you? This contract manufacturer of finished medical devices is adding to their team. Interested in a great new career opportunity with the potential to save and improve lives?

The Perks!

· Up to $130K salary!

· Up to $20K Sign-on Bonus!

· Medical, Dental, Vision

· 401(k) plan with up to 6% match

· Vacation

· And much more!

We’re Recourse Communications and we match top talent with top opportunities. As a QA Engineer II with our client, you will perform Quality Assurance/Quality Engineering activities to ensure components, finished products, and processes meet established specifications. You will analyze materials and processes, make recommendations, or take action to correct deficiencies. You will support the Quality Policy, ensuring that customer, regulatory, and quality system requirements are met or exceeded. You will develop Control Plans, Inspection Instructions, and other documents as needed to effectively manage product and process quality, both internally and at the suppliers. You will develop and review documented operating procedures associated with material inspection or processes. You will support Engineers to develop manufacturing in‐process inspections and perform In‐process, incoming, and final inspections. You will conduct and review inspections onto tubing extrusions. You will participate in the review and approval of Document Change Notice. You will collect, analyze, and interpret statistical data and assist in the design of Experiments and Statistical Process Control to improve processes and products.

About You

  • Bachelor’s of Science in Engineering or equivalent degree
  • 2 years of experience as an Engineer, preferred in the medical device industry
  • Quality Engineering capacity or equivalent work experience (internships and co‐ops considered)
  • Familiar with FDA regulations and Engineering Standards (ISO 13485 familiarity preferable)
  • Experience in Root Cause Analysis Methodology
  • Ability to read and interpret engineering drawings and GD&T symbols and to create 3D models and detail drawings in SolidWorks or equivalent CAD tool
  • Knowledge and understanding of medical devices especially catheters and Good Manufacturing Practice (GMP)
  • Knowledge of validation and statistics
  • Excellent problem‐solving, troubleshooting and verbal and written communication skills
  • Ability to work in a fast‐paced contract manufacturing environment and to work on a multiple project simultaneously
  • Comfortable with MS Office Package, Minitab, and other software
  • A results-oriented, quick learner capable of responding to the urgent needs of the team

About the Company

The Company is a leading contract manufacturer of finished medical devices, specializing in catheter-based medical devices, delivery systems, custom medical tubing, and related minimally invasive surgical products.

Apply Now

There’s no better time than nowto grow your career! Click “Apply Now” to submit your updated resume for consideration.

Equal Opportunity Employer

Job Type: Full-time

Benefits:

  • 401(k) matching
  • Dental insurance
  • Health insurance
  • Paid time off
  • Vision insurance

Schedule:

  • Day shift

Education:

  • Bachelor's (Preferred)

Experience:

  • Root Cause Analysis Methodology: 1 year (Preferred)
  • validation and statistics: 1 year (Preferred)
  • Quality Engineering capacity: 1 year (Preferred)

Work Location: One location




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