Validation Engineer – CSV & GxP Systems Lead

GlaxoSmithKline; SITE Town; On-site; PKR 1,200,000 - 1,800,000; Full time

Job summary

A global biopharma company in Pakistan is seeking a validation specialist to lead validation lifecycle activities. This on-site role requires expertise in computerized system validation, with a minimum of 3 years in a regulated environment. Candidates must possess a degree in Engineering or Science and have strong communication skills to work with cross-functional teams. Join a team focused on practical improvements and growth.

Qualifications

• Minimum 3 years’ experience in validation in a regulated environment.
• Experience with IQ/OQ/PQ activities and preparing validation protocols.
• Strong written and verbal communication skills.

Responsibilities

• Plan and execute validation lifecycle activities.
• Ensure compliance with Computerized System Validation (CSV).
• Prepare validation documents and maintain validation tracker.

Skills

Validation lifecycle activities

Computerized System Validation (CSV)

Report writing

Technical support for utilities

Cross-functional teamwork

Education

Bachelor’s degree in Engineering or Science

Tools

MS Office

Validation or quality management software

Job description

A global biopharma company in Pakistan is seeking a validation specialist to lead validation lifecycle activities. This on-site role requires expertise in computerized system validation, with a minimum of 3 years in a regulated environment. Candidates must possess a degree in Engineering or Science and have strong communication skills to work with cross-functional teams. Join a team focused on practical improvements and growth.