5 - 10 Years
Not Disclosed
Full Time - Permanent
Vapi

Views:57

Applicants:1

Posted on 23 Jun, 2025

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

Overview
  • Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO, Biotech / Biopharmaceuticals
  • Functional Area - Quality - QC / QA / QMS / TQM / Lean / Six Sigma
  • Job Role - Quality Compliance Manager
  • Employment type - Full Time - Permanent
  • Work Mode - In Office
Job Description | Role and Responsibilities

  • Monitor GMP adherence in manufacturing, packaging & storage

  • Audit processes, equipment & training; resolve compliance gaps

  • Review & approve batch records, SOPs, deviations/CAPAs

  • Train staff; update GMP materials; build quality culture

  • Support regulatory audits; implement findings

  • Improve processes while ensuring cleanroom & API handling

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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