Pharma Validation Engineer - CSV & Commissioning

GSK plc; Pakistan; On-site; PKR 1,200,000 - 1,800,000; Full time

Job summary

A global biopharma company is seeking a Validation Engineer for their site in Pakistan. The role involves planning and executing validation activities, ensuring compliance with regulations, and preparing necessary documentation. Candidates should have a Bachelor's degree in Engineering or Science and a minimum of 3 years of experience in validation. Strong communication and teamwork skills are essential. This position requires regular on-site presence to lead validation and commissioning activities.

Qualifications

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

Responsibilities

• Plan and execute validation lifecycle activities including IQ, OQ, and PQ.
• Ensure CSV is maintained for all GxP and Non-GxP equipment.
• Prepare and maintain validation documents like protocols and reports.

Skills

Validation lifecycle activities

Computerized System Validation (CSV)

Proficiency in MS Office

Strong communication skills

Education

Bachelor's degree in Engineering or Science

Tools

Kneat

SCADA systems

Job description

A global biopharma company is seeking a Validation Engineer for their site in Pakistan. The role involves planning and executing validation activities, ensuring compliance with regulations, and preparing necessary documentation. Candidates should have a Bachelor's degree in Engineering or Science and a minimum of 3 years of experience in validation. Strong communication and teamwork skills are essential. This position requires regular on-site presence to lead validation and commissioning activities.