Validation Engineer

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.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• 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.

Why You?

Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals

• 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
If you have the following characteristics, it would be a plus

• 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.

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.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• 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.

Why You?

Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals

• 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
If you have the following characteristics, it would be a plus

• 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.

Dlaczego GSK?
Łączymy naukę, technologię i umiejętności, aby razem pokonywać choroby.

GSK to globalna firma biofarmaceutyczna, której celem jest łączenie nauki, technologii i talentów, aby razem pokonywać choroby. Jako odnosząca sukcesy, rozwijająca się firma, w której ludzie mogą realizować swój potencjał, dążymy do pozytywnego wpływu na zdrowie 2,5 miliarda ludzi do końca dekady.

Priorytetem są dla nas innowacyjne rozwiązania w obszarze szczepionek i leków specjalistycznych, które maksymalizują rosnące możliwości w zakresie zapobiegania chorobom i ich leczenia. 

Skupiamy się na czterech obszarach terapeutycznych: układzie oddechowym, immunologii; onkologii; HIV; oraz chorobach zakaźnych – aby wpływać na zdrowie na dużą skalę.

Ludzie i pacjenci na całym świecie polegają na lekach i szczepionkach, które produkujemy, dlatego zobowiązujemy się do tworzenia środowiska, w którym nasi pracownicy mogą się rozwijać i koncentrować na tym, co najważniejsze. Nasza kultura bycia ambitnym dla pacjentów, odpowiedzialnym za wpływ i postępowania właściwie jest fundamentem, na którym wspólnie dostarczamy rezultaty dla pacjentów, akcjonariuszy i naszych pracowników.

Dane kontaktowe:
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Ważna informacja dla biur/agencji pośrednictwa pracy
GSK nie akceptuje poleceń pracowników od biur i/lub agencji pośrednictwa pracy w odniesieniu do ofert pracy zamieszczonych na tej stronie. Wszystkie biura/agencje pośrednictwa pracy są zobowiązane do skontaktowania się z działem handlowym i ogólnym/kadr GSK w celu uzyskania wcześniejszej pisemnej zgody przed poleceniem kandydatów firmie GSK. Uzyskanie uprzedniej pisemnej zgody jest nadrzędne w stosunku do jakiejkolwiek umowy (ustnej lub pisemnej) między biurem/agencją pośrednictwa pracy a GSK. W przypadku braku takowego pisemnego upoważnienia wszelkie działania podejmowane przez biuro/agencję pośrednictwa pracy będą uważane za wykonane bez zgody lub umownego porozumienia ze strony GSK. GSK nie ponosi zatem odpowiedzialności za jakiekolwiek opłaty wynikające z takich działań lub wynikające z polecenia danej osoby przez biura/agencje pośrednictwa pracy w odniesieniu do ofert pracy zamieszczonych na tej stronie.