INSPYR Solutions is looking for Quality Control Specialist in Lewisville, TX. This local job opportunity with ID 3662912323 is live since 2026-05-04 14:28:34. Title: Quality Control Specialist Location: Lewisville, TX (on site) Duration: 6 month contract to hire Compensation: $35-41/hour Work Requirements: US Citizen, GC Holders or Authorized to Work in the U.S. Position Overview
This role supports supplier quality assurance activities for outsourced products, materials, and services. The position ensures that all suppliers comply with applicable regulatory standards and established quality requirements. Responsibilities include conducting supplier audits, managing corrective actions, maintaining supplier data systems, and supporting quality agreements.
The role also participates in new product development initiatives, represents quality functions in cross-functional teams, and serves as a key contact for supplier quality and compliance matters. The objective is to resolve quality issues, strengthen supplier performance, and enhance global quality standards.
Minimum Qualifications
Education Bachelor's degree in a scientific or technical discipline such as Science, Technology, Engineering, Mathematics, or a closely related field.
Experience
Minimum of 5 years of experience in Quality, Engineering, or Manufacturing within a GMP-regulated environment (e.g., pharmaceuticals, OTC products, personal care, or dietary supplements)
At least 3 years of auditing experience
Certifications
One or more of the following certifications (or equivalent) is required:
Certified Quality Auditor (CQA)
Certified Quality Engineer (CQE)
Certified Food Safety Quality Auditor (CFSQA)
Certified Pharmaceutical GMP Professional (CPGP)
Preferred:
Preventive Controls Qualified Individual (PCQI)
Key Responsibilities
Maintain and update supplier/manufacturer data within internal systems, ensuring accuracy and completeness of assessment-related information
Analyze supplier performance metrics and trends to proactively identify risks or issues
Participate in cross-functional continuous improvement initiatives to enhance supplier quality and performance
Develop audit plans and conduct assessments of new and existing global suppliers (including ingredients and component providers) to verify compliance with regulatory and quality standards
Ensure timely communication and documentation of audit findings
Review, track, and manage supplier corrective action plans through to completion
Act as a quality representative on supplier audits, projects, and new product development teams
Serve as a subject matter resource for supplier quality across global operations
Collaborate with regional teams to support local manufacturing, sourcing, and training while ensuring adherence to internal quality policies
Support internal audits of manufacturing and distribution sites, as well as international operations
Assist with external regulatory inspections and audits conducted by agencies such as the FDA and other governing bodies
Quality systems, audit methodologies, inspection processes, and data integrity principles
Familiarity with quality requirements in industries such as personal care, OTC products, and dietary supplements
Ability to manage multiple projects and prioritize tasks effectively to meet deadlines
Experience with continuous improvement tools and methodologies
Strong analytical thinking and problem-solving skills
Ability to work independently with minimal supervision and general direction
Proven effectiveness in a matrixed, global environment spanning multiple regions and cultures
Excellent written and verbal communication skills, with the ability to clearly convey risks and issues to diverse stakeholders
Proficiency in Microsoft Office tools, including:
Word
Excel (data analysis and management)
Outlook
Teams
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