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)

• As Passionate Transformers , we find a better way to innovate relentlessly.
• Being Mission Driven, we consistently deliver on our promises.
• Our Entrepreneurial spirit makes the most of EVERY opportunity for innovation.
• Understanding that Relationships Matter creates synergies that yield the greatest benefits for all.
• In Doing the Right Thing , we lead by example in ALL we do.