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Quality Assurance Specialist

Job in Round Rock, Williamson County, Texas, 78682, USA
Listing for: Trident Consulting
Full Time position
Listed on 2026-09-15
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Data Analyst, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 33 - 37 USD Hourly USD 33.00 37.00 HOUR
Job Description & How to Apply Below

Trident Consulting is seeking a   
Quality Assurance Specialist  for one of our clients, A global science and technology company

Job Title:

Quality Assurance Specialist
Duration:12+Month Contract (Contract to hire)
Pay rate:$33-$37/hr on W2

Schedule :
Monday–Friday, 8:00 AM–5:00 PM CST

We are looking for an experienced Quality Assurance Specialist to support quality operations in a regulated environment. The ideal candidate will have strong experience with quality documentation, batch record review, audits, validation, SOPs, and quality systems

Key Responsibilities
  • Review and approve batch records, quality documents, validation records, stability records, and raw material records
  • Review equipment qualifications, calibration records, analytical methods, and method validations
  • Prepare and review Certificates of Analysis (CoA)
  • Support customer, ISO, DEA, and internal audits
  • Review and approve SOPs for quality and regulatory compliance
  • Identify documentation discrepancies and compliance issues
  • Support quality investigations, CAPA, and Root Cause Analysis (RCA)
  • Prepare quality metrics and reports
  • Support quality-system initiatives and continuous improvement
Required Qualifications
  • Bachelor's degree in Chemistry, Biology, Life Sciences, or related field
  • 5+ years of QA experience in an ISO, GMP, or similarly regulated environment
  • Strong experience with quality documentation and batch record review
  • Excellent attention to detail and analytical skills
  • Experience identifying discrepancies between procedures, documentation, and quality requirements
  • Strong written and verbal communication skills
Preferred Experience
  • Pharmaceutical / Biotech / Clinical / Laboratory experience
  • ISO 9001, ISO 17025, ISO 17034, ISO 14001
  • GMP / GxP quality systems
  • Validation and qualification activities
  • Veeva or similar eQMS
  • CAPA, deviations and Root Cause Analysis
  • Internal and external audit experience
Important

This is a 100% onsite position
. Candidates must be comfortable working onsite in a regulated manufacturing/laboratory environment.

About Trident Consulting

Trident Consulting is an award-winning staffing and consulting firm headquartered in San Ramon, CA. Since 2005, we’ve partnered with Fortune 500 and high-growth companies to deliver high-quality talent across technology, engineering, business operations, and professional services.

We specialize in contract, contract-to-hire, and direct hire placements, supporting roles across IT, data & analytics, cloud, cybersecurity, finance & accounting, HR, operations, and more. With a strong focus on hard-to-fill and niche positions, our global recruiting engine enables us to deliver speed, quality, and scale

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