Compliance Engineer

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About the role

Job Title: Compliance Engineer 14 Month Fixed Term Contract FTC Role Purpose: The purpose of this role is to ensure adherence to company and regulatory standards for Environment, Health & Safety (EHS), Quality, and Engineering. By leveraging continuous improvement methodologies, the role will drive sustainable enhancements to existing compliance systems and processes, ensuring compliance requirements across engineering are consistently met. Key Responsibilities: • Own and drive compliance with Quality Management Systems and Safety systems within Engineering. • Management and governance of engineering safety and quality Key Performance Indicators (KPI’s). • Provide management and oversight of the following key compliance areas within Engineering: Engineering Standards (ES), Quality Management System (QMS), Eng Alerts, Legionella, Asbestos, TP13, Technical Authority, Risk Management, Maturity Assessments. • Ensure documentation periodic review and retention is managed. • Manage the department Self Inspection Audit/Management Monitoring program. • Ownership of the Engineering Change Control and Planned Change process • Support Good Manufacturing Practices ( GMP) and safety audits including fronting as required. • Manage and chair department councils & engineering governance meetings. • Deliver GMP training as required for the department. Basic Qualifications: • A-Levels or a Foundation Degree in an engineering discipline, or equivalent experience. • Experience in Quality Management System principles and engineering standards • Experience in organizing workload effectively and manage multiple tasks • Experience preparing and delivering written and verbal communications in English in a professional setting • Experience working with cross-functional teams to achieve shared objectives. • Experience creating presentations in Microsoft PowerPoint and analysing data using Microsoft Excel. • Experience working in a pharmaceutical manufacturing environment operating under cGMP and Quality Management Systems (QMS). Preferred Qualifications: • Higher National Certificate or Degree or equivalent experience in relevant engineering related subject • To enable the individual to manage compliance within a complex GMP environment Work Arrangements: Based Barnard Castle This role is on-site, 5 days per week. Closing Date for Applications: 20/10/2026 Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application. #LI-GSK Skills Asset Life Cycle Management, Data Integrity, Digital Fluency, GxP Regulations, Lean Management, Manufacturing Technologies, Pharmaceutical Manufacturing, Problem Solving, Risk Awareness, Standards Compliance     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 fo

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