Senior QA Operations Lead — Batch Release & Compliance

Centrient Pharmaceuticals Netherlands

Dera Ghazi Khan Division

On-site

PKR 1,800,000 - 2,600,000

Full time

4 days ago
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Job summary

Centrient Pharmaceuticals Netherlands is seeking an experienced QA Operations professional to review Batch Production Records, issue and review product labels, and oversee release of finished products. The role requires API experience and strong CAPA/Investigations capabilities.

The candidate will report to the Manager - QA Operations and will participate in audits, calibration activities, and site verification processes to ensure compliance with GMP and safety standards.

Qualifications

  • MSc in Chemistry or M.Pharma required.
  • Experience: 10–15 years with API exposure.
  • Review and approval of Batch Production Records and investigations.

Responsibilities

  • Review Batch Production Records and approve investigations.
  • Release or reject finished products per approved specs.
  • Verify QC test results and batch disposition, quarantine as needed.
  • Release/Reject finished products as per specifications.
  • Calibration & maintenance QA oversight.
  • Perform cleaning verification during product changeovers.
  • Verify reprocessing activities at the site.
  • Handle sale returns.
  • Comply with Safety, Health & Environment norms.
  • Assign tasks as directed by supervisor.

Skills

QA Oversight
CAPA & Deviations
OOS/OOT Investigations
Batch Review & Release
QC Test Results Review
Calibration & Maintenance
GMP & Compliance
Safety & Environment

Education

MSc in Chemistry or M.Pharma

Job description

Centrient Pharmaceuticals Netherlands is seeking an experienced QA Operations professional to review Batch Production Records, issue and review product labels, and oversee release of finished products. The role requires API experience and strong CAPA/Investigations capabilities.

The candidate will report to the Manager - QA Operations and will participate in audits, calibration activities, and site verification processes to ensure compliance with GMP and safety standards.

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