QA Validation Engineer

CEVA Logistics
Swadlincote, United Kingdom
2 days ago

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Working hours
Shift work
Languages
English, Dutch
Experience level
Senior
Compensation
£ 37K

Job location

Swadlincote, United Kingdom

Tech stack

iOS
Supervisory Control and Data Acquisition (SCADA)
Iq/oq/pq

Job description

YOUR ROLEAre you passionate about quality, compliance, and ensuring that critical facilities and equipment operate to the highest standards? At CEVA Logistics, we are looking for a QA Validation Engineer to support the commissioning and qualification of new GDP/GMP facilities, including ISO 7 and ISO 8 cleanrooms.This role is essential to ensuring our systems, equipment, and environments operate safely, effectively, and in full compliance with all regulatory expectations. You will collaborate with internal teams, suppliers, and external partners to deliver robust validation activities across new and existing facilities.WHAT ARE YOU GOING TO DO?In this role, you will carry out validation and qualification activities for new GDP/GMP facilities, equipment, cleanrooms, and systems. You will review and approve validation protocols (IQ/OQ/PQ), assess vendor documentation, manage deviations, and ensure all validation activities meet internal standards and regulatory requirements.You will perform GAP analyses, support risk and impact assessments, monitor changes to validated systems, and guide decisions on revalidation needs. You will also contribute to SOP updates, environmental monitoring support, and process improvement initiatives.Working closely with project teams, you will help plan, schedule, and deliver validation tasks on time, including supporting the validation of automation systems and warehouse management systems.WHAT ARE WE LOOKING FOR?We are seeking a detail driven, analytical QA professional with experience in facilities and equipment validation within a GMP environment. You will bring strong knowledge of cleanroom qualification, commissioning processes, and validation standards across manufacturing and GDP facilities.You should have a solid understanding of MHRA and FDA regulations, strong technical writing capabilities, and the ability to communicate effectively across diverse teams. You'll be someone who thrives under pressure, uses sound judgement to solve problems, and contributes positively to project environments.A Bachelor's degree in science or engineering is required, along with experience in facility/equipment qualification and validation. Experience in commissioning new facilities, automation validation, and quality systems is highly desirable.WHAT DO WE HAVE TO OFFER?We offer a competitive benefits package, a supportive team culture, and the opportunity to play a key role in the development and validation of critical facilities across our network. You'll work in a dynamic, compliance-driven environment with opportunities to grow your expertise in validation, quality systems, and regulated operations.You will also benefit from our rewards platform, life assurance, pension scheme, and professional development pathways designed to support your long-term success.ABOUT TOMORROWWe invest in your future. With numerous opportunities across our global operation and a strong commitment to professional development, we offer a pathway for you to grow, learn, and lead within CEVA Logistics.Join CEVA for a challenging and rewarding career. Similar jobs, YOUR ROLE Are you passionate about quality, compliance, and ensuring that critical facilities and equipment operate to the highest standards? 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