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DAWAR CONSULTING INC

Quality Systems Specialist III

DAWAR CONSULTING INC

. Compile and organize quality data and metrics to support Quarterly Executive Management Reviews .

Posted 9/17/2026contractRemote • California • United StatesMid-LevelSenior💰 $65 - $68 per hourWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Quality Management Systems, including Veeva QMS, with a strong ability to analyze quality data and trends for executive reporting. Proven skills in developing professional presentations and managing cross-functional collaboration in a regulated environment.

Highest-signal resume keywords
Veeva QMS ExperienceQuality Management ReviewsMicrosoft PowerPoint SkillsQuality Metrics AnalysisGxP/GMP Regulatory Experience

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Quality SystemsQuality ManagementData AnalysisQuality MetricsDocument ControlDeviation ManagementCAPAChange ControlManagement ReportingExecutive-Level Presentations
Soft Skills
Strong Organizational SkillsExcellent Communication SkillsCross-Functional Coordination
Tools & Technologies
Veeva Quality DashboardsMicrosoft PowerPoint
Industry Keywords
PharmaceuticalBiotechnologyMedical DeviceLife SciencesGxPGMP

About the role

Key responsibilities & impact
  • Compile and organize quality data and metrics to support Quarterly Executive Management Reviews
  • Develop professional PowerPoint presentations using input and data from global business and Quality stakeholders
  • Coordinate and manage inputs, timelines, and deliverables from cross-functional contributors
  • Collaborate with global Quality teams to ensure timely and accurate completion of Management Review deliverables
  • Review Quality System reports, dashboards, and metrics in Veeva QMS to support executive-level reporting and presentations
  • Analyze and summarize quality trends and data for management review discussions
  • Provide general support for QMS processes, including Deviation Management, CAPA, Document Control, and Change Control
  • Track action items and follow up with stakeholders as needed
  • Support continuous improvement and other Quality Systems activities as assigned

Requirements

What you’ll need
  • Bachelor's degree in Life Sciences, Quality, Engineering, or a related field
  • 5+ years of experience in Quality Systems and/or Quality Management within the pharmaceutical, biotechnology, medical device, or life sciences industry
  • Demonstrated experience supporting Quality Management Reviews / Management Review processes
  • Hands-on experience with Veeva QMS is required
  • Strong Microsoft PowerPoint skills with experience developing executive-level presentations
  • Experience working with Quality metrics, dashboards, and management reporting
  • Strong organizational skills with the ability to manage multiple deliverables and deadlines
  • Ability to coordinate effectively with global and cross-functional stakeholders
  • Excellent written and verbal communication skills
  • Experience with Document Control, Deviations, CAPA, and Change Control
  • Experience working in a GxP/GMP-regulated environment
  • Experience presenting or preparing materials for senior/executive Quality leadership
  • Experience with Veeva Quality dashboards and reporting
  • Experience supporting global Quality organizations
  • Availability for PST Hours

Benefits

Comp & perks
  • Medical
  • Paid Sick Leave
  • 401 (k)