Quality Engineer - Hybrid

Stryker•Redmond, WA

1d•Hybrid

About The Position

Genesis10 is seeking a Quality Engineer for a hybrid position with a Global Medical Technology Company in Redmond, WA. This is a 12+ month contract opportunity. This role is an individual contributor focused on developing and implementing methods for process control, process improvement, testing, and inspection to ensure product quality. The engineer will analyze reports and defective products to identify trends, recommend corrective actions, and collaborate with suppliers on quality improvement initiatives.

Requirements

Engineering degree or equivalent
A minimum of 2 or more years of relevant experience
Ability to work on site 4 days a week
Understanding and application of procedures and concepts of own discipline
Attention to detail in making evaluative judgements based on the analysis of factual information

Responsibilities

Work closely with Operations and business functions to ensure quality performance of product and processes
Collaborate with internal cross-functional and supplier teams to address top quality issues
Own identified internal and supplier-driven Non-Conformances (NC) and Corrective Action Preventative Action records (CAPA), managing the timely processing and closure within the Trackwise system
Support execution and analysis of manufacturing related complaint investigations and product field actions
Investigate and disposition internal non-conforming product within MRB
Communicate and collaborate with suppliers regarding non-conformances, escalating Supplier Corrective Action Requests (SCAR) as required
Execute and manage Supplier Initiated Change Requests (SICRs) received from suppliers
Support manufacturing transfers to or from other facilities, executing appropriate quality activities
Engage in the development and improvement of internal manufacturing and distribution processes for existing products
Perform critical assessments and qualifications of internal and supplier-proposed change management activities, including Production Part Approval Process (PPAP)
Participate in and potentially lead the creation and/or review of new or modified procedures
Support the development and review of process and equipment validation/qualification and MSA of internal processes
Maintain KPIs for monitoring of process and/or product quality, perform analysis, and interpret trends

Benefits

Access to hundreds of clients, most who have been working with Genesis10 for 5-20+ years.
The opportunity to have a career-home in Genesis10; many of our consultants have been working exclusively with Genesis10 for years.
Access to an experienced, caring recruiting team (more than 7 years of experience, on average.)
Behavioral Health Platform
Medical, Dental, Vision
Health Savings Account
Voluntary Hospital Indemnity (Critical Illness & Accident)
Voluntary Term Life Insurance
401K
Sick Pay (for applicable states/municipalities)
Commuter Benefits (Dallas, NYC, SF, and Illinois)