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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 fitCore 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
Tailor your resumeApplicant 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)