1 - 3 Years
Not Disclosed
Full Time - On Contract
Holly Springs, USA, United States of America

Views:207

Applicants:0

Posted on 21 Jun, 2025

Sorry, this vacancy has been closed and is no longer accepting applications.

Overview
  • Industry - HR Staffing & Recruitment Firms / Employment Agency / Background - Reference Check Firms
  • Functional Area - Quality - QC / QA / QMS / TQM / Lean / Six Sigma
  • Job Role - Quality Assurance Lead
  • Employment type - Full Time - On Contract
  • Work Mode - In Office
Job Description | Role and Responsibilities

  • Review & Approve GMP Documents
  • Ensure document adequacy and alignment with GMP standards.
  • Report updates to senior management.
  • Experience in GMP document review from a Quality role.
  • Ability to interpret and apply GMP regulations.
  • Experience in fast-paced pharmaceutical or medical device environments.

Candidate Profile | Who Can Apply
Education
  • Any Graduate - Any Specialization
  • Any Post Graduate - Any Specialization
  • Any Doctorate - Any Specialization
Job Related Keywords
About Employer

Sorry, this vacancy has been closed and is no longer accepting applications.

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