Sr. Quality Technician

Job Summary

Omnicell is excited to be seeking an experienced Sr. Quality Technician t to join our Quality Operations department. The Sr. 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

• Provide training to peers

• Support a culture of quality in the manufacturing environment

• Understand and support regulatory compliance in particular to 21CFR820 and ISO13485

Additional Responsibilities

• Assist in management of MRB activities including segregation and disposition of materials

• 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 10% (for training as necessary)