Software Quality Engineer

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Company: Katalyst HealthCares and Life Sciences

Location: Irving, TX 75061

Description:

Responsibilities:
  • Review and Approval of software lifecycle (SLC) Deliverables for Regulated applications; Risk Classifications, Requirements, Config/Design Specs, IQ, OQ, PQ, Trace Matrix, Summary Reports etc.
  • Collaborate with the cross-functional teams to build compliance capabilities to assure the quality of the deliverables and ensure the business needs are met.
  • Review of CAPAs, Change Controls and Defects for GxP applications.
  • Working with Global teams and providing audit support.
  • Working with a range of applications/tools including ALM, TrackWise, JIRA, Confluence, and other integration tools.
Requirements:
  • Bachelors with 8+ years of exp. or Master's with 5+ years of exp prefered.
  • Prior experience in regulated industry - GxP systems.
  • Good knowledge of FDA regulations; 21 CFR Part 11, 820, Annex 11, GAMP5, ISO 13485 and ISO 27001.
  • Quality Management Tools and Test Management Tools - TrackWise/ComplainceWire/Veeva, ALM, JIRA etc.
  • Knowledge about Data Integrity and prior audit support experience (Internal/External).
  • Experience working with Software as a Service (SaaS), Infrastructure as a Service (IaaS), Platform as a Service (PaaS), Commercial-off-the-shelf (COTS) and Custom applications.

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