Senior QA Associate – GMP & Microbiology

ADP, Inc.

Dallas (TX)

On-site

USD 65,000 - 85,000

Full time

14 days+

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Job summary

ADP, Inc. in Dallas seeks a Quality Associate III to perform advanced QA functions within cGMP programs and supervise/coach QC Inspectors. The role centers on ensuring products meet regulatory and quality specifications and leading training on quality processes.

Responsibilities include GMP reviews, COA documentation, AQL testing, and cross-functional collaboration to resolve issues promptly and maintain product disposition timelines.

Qualifications

  • 5+ years quality experience in a cGMP or regulated industry
  • 3+ years in a Microbiology Lab (microbiology data mgmt)
  • Experience in OTC Drug / Cosmetic / Medical Device manufacturing preferred
  • Ability to read, write, and understand English
  • Must have high integrity, accuracy, and attention to detail
  • Excellent verbal and written communication skills

Responsibilities

  • Execute timely GMP review for Production Records, ensuring documentation compliance.
  • Create and issue Finished Good Lot codes and train Inspectors.
  • Release materials, products, equipment and facilities per QMS processes.
  • Perform, audit, verify, document and report AQL inspections and testing.
  • Prepare COA documentation as required.
  • Escalate quality issues to leadership and coordinate actions for resolution.
  • Interface with cross-functional teams to ensure cGMP compliance.

Skills

Quality control
Attention to detail
Regulatory compliance
Cross-functional teamwork
Documentation

Education

High school diploma or equivalent

Tools

SAP
Quality Management System Software
Microsoft Outlook
Microsoft Word
Microsoft Excel
TEAMS

Job description

ADP, Inc. in Dallas seeks a Quality Associate III to perform advanced QA functions within cGMP programs and supervise/coach QC Inspectors. The role centers on ensuring products meet regulatory and quality specifications and leading training on quality processes.

Responsibilities include GMP reviews, COA documentation, AQL testing, and cross-functional collaboration to resolve issues promptly and maintain product disposition timelines.

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