About Ecolab
A trusted partner at nearly three million customer locations spanning over 170 countries, Ecolab is the global leader in water, hygiene and infection prevention solutions and services. Our team delivers comprehensive solutions, data-driven insights and personalized service to advance food safety, maintain clean and safe environments, optimize water and energy use, and improve operational efficiencies and sustainability for customers in the food, healthcare, hospitality and industrial markets.
When you come to work at Ecolab, you get to take on some of the world’s most meaningful challenges and have the opportunity to learn and grow, shape your career, make an impact and quickly see the importance of your work.
As the Validation Service Engineer, you will execute validation and routine verification activities that support the compliant manufacture of disinfectant products and the ongoing control of validated processes, equipment, and environments. The role is focused on protocol execution, accurate data capture, deviation reporting, and supporting the site in maintaining a validated and inspection-ready state.
What’s in it For You:
The opportunity to take on some of the world’s most meaningful challenges, helping customers achieve clean water, safe food, abundant energy and healthy environments
The ability to make an impact and shape your career with a company that is passionate about growth
The support of an organization that believes it is vital to include and engage diverse people, perspectives and ideas to achieve our best
What you'll do:
Carry out validation and revalidation activities for manufacturing processes, cleaning methods, disinfectant preparation steps, and associated equipment in line with approved protocols.
Support qualification activities for equipment, utilities, and controlled environments used in production, storage, and handling operations.
Complete protocol steps, data sheets, sampling records, and supporting documentation accurately and in real time.
Record process observations, test results, and critical parameters against defined acceptance criteria and escalate any anomalies promptly.
Support execution of efficacy, contact time, surface coverage, or environmental verification activities where required by site procedures.
Assist with investigations linked to validation failures, out-of-limit findings, deviations, or changes affecting validated systems.
Prepare validation packs, check equipment and materials readiness, and coordinate practical execution with production, laboratory, engineering, and quality teams.
Contribute to periodic review, requalification planning, and maintenance of the site validation schedule.
Maintain controlled records in line with GDP, data integrity requirements, and internal document standards.
Identify opportunities to improve validation execution, document flow, and operational compliance.
Realise service maintenance and Installation qualification / operation qualification (IQ/OQ) of the equipment.
What you'll need:
Educated to NVQ, BTEC, HNC, A-level, or equivalent in a scientific, engineering, manufacturing, or technical discipline.
Experience in a regulated manufacturing, laboratory, pharmaceutical, chemical, hygiene, or disinfectant production environment is desirable.
Practical exposure to validation, equipment qualification, cleaning verification, or GMP-controlled documentation would be advantageous.
Experience following standard operating procedures (SOP's) and completing documentation to a high standard in a controlled environment.
Familiarity with deviation reporting, Corrective and preventive action ( CAPA) support, or change control in a regulated setting would be beneficial.
Good working knowledge of Good Manufacturing practice (GMP), hygiene control, and validation requirements within a regulated production environment.
Understanding of process validation, cleaning validation, equipment qualification, and routine verification principles.
Ability…