Back to Jobs
Views:62
Applicants:1
Posted on 23 Jun, 2025
In Office
Job Description | 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
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
Qualifications
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
GMP Coordinator
Routine Audits & Inspections
CAPA / Change Control / Deviation Management
Environmental & Cleanroom Monitoring
Equipment Qualification & Calibration
Regulatory Inspection Support (FDA
EMA)
