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Quality Engineer

Job in Redmond, King County, Washington, 98052, USA
Listing for: Actalent
Full Time position
Listed on 2026-08-31
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Production QC/QA
Job Description & How to Apply Below

Quality Engineer

This role focuses on ensuring the consistent quality performance of products and processes by working closely with Operations and cross-functional business partners. The Quality Engineer manages non-conformances and CAPA activities, supports supplier quality and change management, and drives process improvements and validations in a live production environment. The position requires a balance of supplier quality and product/manufacturing quality experience, strong root cause analysis skills, and the ability to operate effectively in a fast-paced, highly regulated setting.

Responsibilities
  • Work closely with Operations and other business functions to ensure the quality performance of products and processes.
  • Collaborate with internal cross-functional teams and suppliers to address top quality issues and drive effective resolutions.
  • Own identified internal and supplier-driven Non-Conformances (NC) and Corrective Action Preventive Action (CAPA) records, ensuring timely processing and closure within the electronic quality management system (e.g., Track Wise).
  • Support the execution and analysis of manufacturing-related complaint investigations and product field actions, ensuring robust documentation and follow-up.
  • Investigate internal non-conforming product within the Material Review Board (MRB) process and issue NCs as appropriate, including disposition of non-conforming materials.
  • Communicate and collaborate with suppliers regarding non-conformances and escalate Supplier Corrective Action Requests (SCAR) as required.
  • Execute and manage Supplier Initiated Change Requests (SICRs), engaging cross-functional teams for technical assessment, risk evaluation, and approval.
  • Support manufacturing transfers to and from other plants or facilities by executing appropriate quality activities and ensuring compliance with applicable procedures.
  • Collaborate with stakeholders to identify and implement opportunities for supplier part certification to improve incoming quality and efficiency.
  • Engage in the development and improvement of internal manufacturing and distribution processes for existing products, focusing on quality, robustness, and efficiency.
  • Perform critical assessments and qualifications of internal and supplier-proposed changes, including conducting or supporting Production Part Approval Process (PPAP) activities for supplier changes.
  • Participate in and, when appropriate, lead the creation, revision, and review of new or modified procedures related to quality, manufacturing, and supplier management.
  • Support the development and review of process and equipment validation and qualification activities, as well as Measurement System Analysis (MSA) for internal processes.
  • Maintain key performance indicators (KPIs) for monitoring process and product quality, perform data analysis, interpret trends, and implement appropriate corrective or preventive actions.
  • Support live production issues in real time, helping to keep operations moving while maintaining compliance and product quality.
  • Lead or actively contribute to discussions with stakeholders to explain issues, proposed fixes, and resolution plans in a clear and structured manner.
  • Work independently and as part of cross-functional teams, taking ownership of issues and driving actions to closure.
  • Perform other related duties as assigned to support overall quality and operational objectives.
Essential Skills
  • Balanced experience in both supplier quality and product/manufacturing quality, with approximately a 50/50 focus.
  • Strong experience in root cause analysis, including structured problem-solving methods to identify, contain, and eliminate quality issues.
  • Hands-on experience managing Non-Conformances (NC) and Corrective Action Preventive Action (CAPA) activities from initiation through closure.
  • Demonstrated experience with validation activities for both processes and equipment in a production or regulated environment.
  • Experience handling supplier quality issues and change management, including supplier-initiated changes and internal change orders.
  • Experience managing internal manufacturing issues and changes, ensuring quality and compliance during process updates or transfers.
  • Proficiency with documentation and quality system work, including authoring, reviewing, and maintaining controlled documents.
  • Ability to support live production issues, pivot quickly, and keep operations moving while maintaining quality standards.
  • Comfort working in a high-pressure, time-sensitive environment with frequent changes and shifting priorities.
  • Ability to work independently as well as collaboratively across teams, taking ownership and driving actions to completion.
  • Strong communication skills, with the ability to clearly explain issues, root causes, and resolution plans to diverse stakeholders.
  • Comfort leading discussions and influencing stakeholders, including manufacturing, engineering, quality, regulatory, compliance, and suppliers.
  • Naturally curious and investigative mindset, with a strong…
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