Warrendale, PA, USA
5 days ago
Quality Technician

Job Summary

Omnicell is excited to be seeking an experienced Quality Technician to join our Quality Operations department. The Quality Technician will be supporting Production & Supplier Quality teams, in addition to performing inspection activities. This role will be based in Warrendale, PA.

 

Responsibilities

Provide and document dimensional & visual inspection of components and sub-assemblies Perform First Article inspections and documentation Perform pre-production part verification for new product development Report and manage non-conforming product per QMS procedures Maintain identification and traceability of parts per regulatory requirements Maintain documentation for supplier certifications Manage inspection criteria and inventory in computer-based inventory management system Support a culture of quality in the manufacturing environment Understand and support regulatory compliance in particular to 21CFR820 and ISO13485

 

Additional Responsibilities

Assist in calibration activities and maintenance of monitoring and measuring equipment Troubleshoot failures and nonconformities identified in new product development and production Assist Quality Engineers in statistical analysis, investigations, and verification activities

 

Required Knowledge and Skills

Strongly demonstrated documentation skills Knowledge of blueprint reading, using CMM and other precision measuring tools and fixtures Knowledge of AQL levels contained in ANSI standards Metrology Experience Quality Inspection Experience Ability to communicate instructions whether written, spoken, or in a diagram Ability to work collaboratively with peers and team members Strongly demonstrated attention to detail Demonstrated proficiency with common MS office programs (Word, Excel, PowerPoint, Project)

 

Basic Qualifications

High School Diploma/GED and minimum five (5) years of quality work experience Team oriented with strong interpersonal skills

 

Preferred Qualifications

ISO 9001, ISO 13485 or FDA Regulated Medical Device experience Associate degree and minimum three (3) years of quality work experience IPC Certification Certified Quality Inspector (ASQ) SAP and Agile experience CMM programming (Calypso software) GD&T experience

 

Work Conditions

Manufacturing Environment Must be able to lift 30 lbs Daily tasks may include kneeling, squatting, or standing for an extended period of time May travel up to 5% (for training as necessary)

 

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