Senior Pharma QA Engineer
Redmond, WA
Experience: 0
Category: Scientific & Clinical
Contractor Work Model: Onsite
Brand: Joulé
Compensation Range: 70.00 - 53.00 Per Hour
Job ID: 340139
Date Posted: 12/02/2025
Shortcut: http://jobs.systemone.com/D5IEjv
Job Title: Senior Pharma QA Engineer
Location: Redmond, WA
Hours/Schedule: 3:30 PM-2:00 AM Monday - Thursday, flex Friday as needed
Compensation: $46.66- $53.00
Type: Contract
Overview
Global Medical Device company looking to hire experienced Quality Assurance Engineer to join their growing team. This is not an IT role!
Responsibilities
- Work closely with Operations and the business functions to ensure quality performance of product and processes.
- Non-Conformances
- 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 of NC and CAPA records within the electronic management system, Trackwise.
- Support execution and analysis of manufacturing related complaint investigations
- Investigate and disposition internal non-conforming product within MRB, issuing NCs as appropriate.
- Supplier Activities
- Communicate & 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, engaging with cross-function teams for assessment and approval
- Collaborate with appropriate stakeholders to identify and execute opportunities for supplier part certification.
- Process Improvements/Validation
- Engage in the development and improvement of the 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) activities for supplier changes.
- 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, identifying and activating on appropriate actions as necessary.
- Perform other related duties as assigned.
Requirements
- Bachelor’s degree in an Engineering/Science/technical field or a related field
- 1-3 years of experience in quality assurance
- Medical Device experience is highly preferred
Benefits
System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.
Ref: #558-Scientific
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