Validation Service Engineer – GMP Compliance & Process Validation

Ecolab; England; Presencial; GBP 35.000 - 52.000; Jornada completa

Descripción de la vacante

Ecolab in the United Kingdom is seeking a Validation Service Engineer to perform validation and routine verification activities that support the compliant manufacture of disinfectant products. The role focuses on protocol execution, accurate data capture, deviation reporting and maintaining validated, inspection-ready state across processes, equipment and environments.

You will collaborate with production, QA and engineering to prepare validation packs, qualify equipment and drive continuous

Formación

• 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 SOPs and completing documentation to a high standard in a controlled environment.
• Familiarity with deviation reporting, CAPA support, or change control in a regulated setting would be beneficial.
• Good working knowledge of GMP, hygiene control, and validation requirements within a regulated production environment.
• Understanding of process validation, cleaning validation, equipment qualification, and routine verification principles.
• Ability to interpret approved protocols, work instructions, specifications, and acceptance criteria.
• Competence in accurate data recording, basic data review, and completion of validation and quality records.
• Awareness of data integrity principles and contemporaneous, legible, and traceable documentation.
• Ability to identify non-standard results and elevate issues in a timely and controlled manner.
• Competent user of standard digital tools used for documentation, data entry, and report preparation.
• Full clean UK driving licence (75% UK / Europe travel)

Responsabilidades

• 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 elevate 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.

Conocimientos

SOP knowledge

Data recording accuracy

GMP awareness

Attention to detail

Data integrity understanding

Communication with teams

Driving licence

Educación

NVQ/BTEC/HNC/A-level or equivalent

Herramientas

Documentation tools

CAPA systems

Deviation reporting tools

Descripción del empleo

Ecolab in the United Kingdom is seeking a Validation Service Engineer to perform validation and routine verification activities that support the compliant manufacture of disinfectant products. The role focuses on protocol execution, accurate data capture, deviation reporting and maintaining validated, inspection-ready state across processes, equipment and environments.

You will collaborate with production, QA and engineering to prepare validation packs, qualify equipment and drive continuous