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Quality Assurance Consultant - Supplier Management

Job in Elwood, Doniphan County, Kansas, 66024, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-09-12
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers
Salary/Wage Range or Industry Benchmark: 75000 - 105000 USD Yearly USD 75000.00 105000.00 YEAR
Job Description & How to Apply Below

Your Role:
Quality Assurance Associate - Supplier Management (Elwood, Kansas)

Responsibilities:
  • Manage QA activities for material movement, including disposition, hold, rejection, and release of incoming materials.
  • Support Manufacturing and Warehouse teams to promote compliance through leadership, collaboration, and day-to-day quality oversight.
  • Own lifecycle management of material and packaging specifications (drafting, annual review, revision updates).
  • Conduct gap assessments for specifications and SOPs.
  • Draft, route, and complete quality system records (change controls, deviations, CAPAs, investigations) in Veeva Quality Management System.
  • Participate in and lead internal and supplier audits; support documentation requests for external regulatory audits.
  • Analyze quality events/investigations/projects and independently resolve complex technical and compliance issues.
  • Represent QA on cross-functional project teams and provide quality guidance.
  • Author/revise quality documents, procedures, and records to maintain regulatory and internal compliance.
  • Conduct SAP transactions to support material release and verify data accuracy.
  • Support records management/archival and assist QA team members as needed.
Qualifications:
  • Bachelor’S degree in a Life Science discipline preferred (or equivalent education/experience).
  • 5+ years in a regulated industry (USDA, FDA, ISO, GMP, or similar) with direct Quality Assurance experience.
  • Strong understanding of quality systems, GMP principles, and applicable regulatory requirements.
  • Experience reviewing/approving quality documentation, investigations, deviations, CAPAs, and change controls.
  • Ability to make sound independent decisions and manage multiple priorities.
  • Strong technical writing, analytical, and problem-solving skills.
  • Excellent verbal and written communication.
  • Proficiency with Microsoft Office (Word, Excel, PowerPoint).
  • Ability to work effectively in a collaborative team environment.
Preferred:
  • Experience with Veeva Quality Management Systems and SAP.
  • Knowledge of risk management tools and basic statistical analysis.
  • Supplier/internal/regulatory audit experience.
Benefits (highlights):
  • Multiple relocation packages; 8-week parental leave; annual bonus; flexible work arrangements; up to 6% 401(k) matching.
Additional info:

Travel 0–5%.

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