Assoc, Quality I - Clinical Trials at Quest Diagnostics Lewisville, TX

Quest Diagnostics

Lewisville, TXFull-timePosted Apr 22, 2026

Behavioral Health Market Context

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Qualifications

  • Excellent verbal and written communication skills
  • Strong organizational skills; very detail oriented and a self-motivated problem solver
  • Knowledge of Microsoft Word, Excel, PowerPoint, and Outlook
  • Required Work Experience
  • 0-2 years' experience in a QA role in a GLP or GCP environment
  • Knowledge of Standard Operating Procedures and Quality Systems principles
  • Knowledge of Standard Operating Procedures and Quality Systems principles
  • Knowledge of document control systems
  • Good verbal and written communication skills; strong interpersonal skills
  • Strong organizational skills; detail oriented
  • Proficiency with Microsoft Office Suite (including WORD, EXCEL)
  • To perform this job successfully, the individual must be able to perform each essential duty satisfactorily
  • The requirements listed above are representative of the knowledge, skill, and/or ability required
  • 10 more items(s)

Responsibilities

  • Exercises judgement within defined areas of responsibility
  • Works on problems of limited scope; performs all duties and responsibilities with direct supervision
  • Under supervision, engages in planned and systematic activities to provide confidence that Quest is fulfilling its requirements for quality and continuous quality improvement
  • Under direct supervision, performs audits of laboratory and study records to ensure compliance with regulatory requirements and company standards
  • Under general supervision, manages the Pharma Services Biopharma Document Control Repository
  • Under general supervision, manages the Pharma Services Biopharma staff training files
  • Manage the Document Control
  • May perform periodic review of Document Control Standard Operating Procedures and forms
  • Review Document Control SOPs & provide feedback to content owner, as needed
  • Manage training files for Pharma Services BioPharma Personnel
  • Participate in the Quality Management Program including, but not limited to:
  • Participate in administrative functions of the QAU (e.g. updating records, maintaining spreadsheets, preparation of reports, filing, etc.)
  • May assist with preparation of quality indicators
  • Auditing & Inspections:
  • Under direct supervision, assist team with, or conduct study audits
  • Under direct supervision, assist with preparation of reports, as applicable
  • 13 more items(s)


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