Validation Engineer

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

We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients. You will validate and qualify equipment, systems, and utilities at our Pakistan site. You will work with engineering, quality, operations and external vendors to plan, execute, and document validation activities. We value people who are careful, curious, and collaborative. You will grow your technical skills, influence site reliability and compliance, and support GSK’s mission of uniting science, technology and talent to get ahead of disease together.

Responsibilities

• Plan and execute validation lifecycle activities including design reviews, installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ).
• Ensure Computerized System Validation (CSV) at the site—including platforms like Kneat and CSQMS—by performing and documenting periodic compliance and validation reviews for all GxP and Non‑GxP equipment, utilities, and facilities, in line with regulatory and corporate requirements.
• Prepare, review and maintain validation documents such as user requirements, validation plans, protocols, reports and traceability matrices.
• Support computerized system validation (CSV) and maintain compliance with site quality systems and validation policies.
• Coordinate commissioning and SAT activities with engineering, operations and external vendors.
• Lead new validation projects (e.g., URS, SIA, RTM, DQ/DR, CVP/IOQ protocols & reports), maintain and update the validation tracker, and ensure all validation documentation is complete, timely, and accessible as per company policies.
• Actively participate in the Validation Working Party (VWP) to follow up on validation targets, resolve issues, and keep the Site Engineering Lead informed, ensuring all validation activities are aligned with defined timelines and standards.
• Collaborate with engineering, operations, and external vendors for commissioning and SAT activities. Offer technical support for utilities and automation systems (e.g., purified water, compressed air, HVAC, PLC‑driven equipment), and engage in risk assessments and root cause analyses.

Basic Qualification

• Bachelor’s degree in Engineering (Mechanical, Electrical, Chemical, Industrial) or Science
• Minimum 3 years’ experience in validation, engineering, or technical roles in a regulated manufacturing environment.
• Experience with IQ/OQ/PQ activities and preparing validation protocols and reports.
• Working knowledge of computerized system validation concepts and familiarity with validation documentation practices.
• Proficiency in MS Office for report writing and data presentation.
• Strong written and verbal communication skills and the ability to work with cross‑functional teams.

Preferred Qualification

• Degree or certification in quality, validation, automation, or related field.
• Experience with PLCs, SCADA systems, and industrial automation.
• Experience using validation or quality management software.
• Knowledge of Pharmaceutical & Sterile Manufacturing Systems and Clean Utilities Systems (Purified Water, HVAC, Steam) and their qualification.
• Experience in project work, commissioning of equipment, or managing vendors.
• Familiarity with regulatory expectations and good documentation practices in manufacturing environments.

Work location and model

This role is on‑site at our Pakistan facility. Regular on‑site presence is required to lead validation and commissioning activities.

What we value

We look for people who take responsibility, work openly with others, and focus on practical improvements. You will join a team that supports learning, growth and inclusion. We encourage clear, respectful communication and collaboration across teams.

Ready to apply?

If you are motivated to build your validation expertise and make an impact, we would like to hear from you. Please submit your CV and a short note explaining why this role interests you. We welcome candidates from varied backgrounds and encourage applications from all qualified people.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Contact information

You may apply for this position online by selecting the Apply now button.