4 - 8 Years
Not Disclosed
Full Time
Mexico, USA, United States of America

Views:3

Applicants:0

Posted on 15 Dec, 2025

Overview
  • Industry - IT - Consulting Services / Advisory Services
  • Functional Area - Other
  • Job Role - Other
  • Employment type - Full Time
  • Work Mode - Hybrid
Job Description | Role and Responsibilities

  • 4+ years of hands-on CSV experience in pharma, biotech, or CRO
  • Deep understanding of GCP/GLP processes and regulatory expectations
  • Proven track record preparing systems and documentation for regulatory audits
  • Strong documentation, communication, and problem-solving skills

Candidate Profile | Who Can Apply
Education
  • Any Graduate - Any Specialization
  • Any Post Graduate - Any Specialization
  • Any Doctorate - Any Specialization
Job Related Keywords
About Employer
Contact Details
Email - info@programming.com

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