
Compliance Engineer (Secondment)
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Job Title: Compliance Engineer
This is a secondment role is for 12 months that offers a unique opportunity to make a meaningful impact while gaining valuable experience.
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 Foundation degree in engineering discipline
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
Working Arrangements:
On site role (not eligible for remote working).
Skills
Asset Life Cycle Management, Data Integrity, Digital Fluency, GxP Regulations, Lean Management, Manufacturing Technologies, Pharmaceutical Manufacturing, Problem Solving, Risk Awareness, Standards ComplianceIf you require an accommodation or other assistance to apply for a job at GSK/ViiV Healthcare, please submit a request to HR via the Service Portal
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
This Position Description is to provide a framework for job understanding between employee and manager. It may not cover or contain the full listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice and at the discretion of the management of the Company. The position description is not used in the assignment or assessment of any GSK level or grade used in the Job Evaluation Process.
Compensation Grade:8Job Posting End Date:10-08-2026Eligible for Employee Referral Bonus:NoSimilar jobs

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