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Sr. Design Quality Engineering

Job in Irvine, Orange County, California, 92713, USA
Listing for: Katalyst CRO
Full Time position
Listed on 2026-01-12
Job specializations:
  • Engineering
    Quality Engineering, Biomedical Engineer
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Sr. Design Quality Engineering

Apply for the Sr. Design Quality Engineering role at Katalyst CRO
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Job Summary

Ensure quality engineering activities for released products comply with regulatory and internal standards while supporting risk management, verification & validation, process validation, and sustaining engineering activities.

Responsibilities
  • Ensure quality engineering activities for released products comply with regulatory and internal standards.
  • Collaborate with cross-functional teams to develop product risk management documentation, including Risk Management Plans, Risk Assessments, DFMEA, and Risk Management Reports.
  • Support the development and execution of Verification and Validation (V&V) plans, protocols, and reports, Test Method Validation, as well as process validation activities (PFMEA, IQ, OQ, PQ) using statistical tools (e.g., Minitab) for data analysis and decision‑making.
  • Oversee product testing and analysis to ensure compliance with applicable standards and requirements.
  • Apply Design Control principles to support sustaining engineering efforts, including design updates and product enhancements.
  • Resolve quality issues, manage design changes, and assess risks in partnership with engineering, manufacturing, and quality teams.
  • Apply risk management techniques to proactively identify and mitigate product risks.
  • Use structured problem‑solving methodologies to address product and process challenges.
  • Communicate findings effectively through presentations, technical reports, and cross‑functional collaboration.
Education & Experience
  • Experience supporting Verification & Validation, process validation, risk management, and sustaining engineering activities.
  • Proficiency in using statistical tools such as Minitab for data analysis.
  • Knowledge and experience applying Design Controls and risk management techniques in engineering environments.
  • Ability to work collaboratively across engineering, manufacturing, and quality teams.
Seniority level

Mid‑Senior level

Employment type

Contract

Job function

Quality Assurance

Industries

Pharmaceutical Manufacturing

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