Pharma Documentation Specialist - GMP & QA Compliance

Mass Pharma (Private) Limited.; Lahore; On-site; PKR 600,000 - 1,000,000; Full time

Job summary

Mass Pharma (Private) Limited. in Lahore, Pakistan is seeking a Documentation Officer to manage GMP-compliant pharmaceutical documents. The role requires a Pharm D and 1–2 years of QA documentation experience.

You will prepare and review SOPs, BMRs, validation protocols, and related records, ensuring regulatory readiness and smooth audits. Collaboration with cross-functional teams is essential for effective document control.

Qualifications

• Pharm D degree from a recognized university.
• 1–2 years of professional experience in pharmaceutical documentation (Quality Assurance)

Responsibilities

• Prepare, review, and maintain pharmaceutical documentation (SOPs, Batch Manufacturing Records, Validation Protocols, etc.) in compliance with GMP guidelines.
• Ensure regulatory compliance and support audit preparations.
• Coordinate with cross-functional teams to manage document control systems efficiently.

Skills

Pharma QA

SOP management

Documentation

Audit support

Education

Pharm D

Job description

Mass Pharma (Private) Limited. in Lahore, Pakistan is seeking a Documentation Officer to manage GMP-compliant pharmaceutical documents. The role requires a Pharm D and 1–2 years of QA documentation experience.

You will prepare and review SOPs, BMRs, validation protocols, and related records, ensuring regulatory readiness and smooth audits. Collaboration with cross-functional teams is essential for effective document control.