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Preclinical Quality Assurance Technician 2

Job in Atlanta, Fulton County, Georgia, 30301, USA
Listing for: Veranex
Full Time position
Listed on 2026-08-20
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Job Description & How to Apply Below

Preclinical Quality Assurance Technician 2

Veranex's mission as an Innovation CRO is to improve patient outcomes by accelerating our clients' innovations to market. As the world's only end-to-end professional services firm focused on Med Tech, we take clients' Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.

About

This Role

The Preclinical Quality Assurance Technician 2 will primarily support study-level Quality Control activities at Veranex Preclinical Services in Atlanta. The position will be aligned with the Quality Assurance department and remain independent from study operations while working directly with study teams to support timely, accurate, and complete study documentation.

What You'll Do
  • Perform contemporaneous and detailed QC reviews of GLP and non-GLP study records, raw data forms, worksheets, logs and reports for completeness, accuracy, consistency, legibility, and compliance with SOP's and Good Documentation Practices (GDP).
  • Verify that study records contain all required signatures, dates, corrections, and supporting documentation.
  • Coordinate with Study Directors and operational personnel to resolve documentation deficiencies prior to QA inspections or record archival.
  • Support review of data tables, calculations, report components, study closure, and archival.
  • Conduct data reconciliation activities in collaboration with study personnel.
  • Maintain QC logs, issue trackers, and study-specific quality records.
  • Support audit and inspection readiness activities.
  • Assist with document control, quality documentation, training, and other QA/QC activities.
  • Assists with the design and updating of quality documentation.
Required Qualifications
  • 2-4 years of relevant work experience.
  • Good knowledge of overall medical device industry.
  • Good understanding of good laboratory practices (GLP) and regulatory policies and governance practices.
  • Associate degree in a relevant field required.
  • Strong attention to detail, organization, consistency, and follow-through.
  • Strong written and verbal communication skills.
  • Ability to work independently and across functional teams.
Location
  • This is an onsite position in Atlanta, GA

Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.

Applicants must be currently authorized to work in the United States on a full-time basis. The company is not able to sponsor visas or provide employment-based immigration sponsorship for this role now or in the future.

Protecting Your Job Search (Recruitment Scam Awareness)

At Veranex, we believe our people are what set us apart, and our commitment to supporting talent begins the moment you consider joining our team. We aim to provide every candidate with a safe and transparent recruiting experience. As phishing and recruitment scams continue to target job seekers worldwide, here are a few items to keep in mind:

  • Official communications will only come from company email addresses ending in
  • We will never ask you to send money or provide banking information at any stage of the recruitment process.
  • Be cautious of unexpected emails and avoid opening suspicious links or attachments.
  • When in doubt, contact us. If you have questions about the authenticity of a communication you've received, please contact our recruiting team at  before responding
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