Liam O'Neill Email & Phone Number
@cbre.com
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Who is Liam O'Neill? Overview
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Liam O'Neill is listed as Associate Director Risk and Compliance at GSK R&D at GSK, based in Stevenage, England, United Kingdom. AeroLeads shows a work email signal at cbre.com and a matched LinkedIn profile for Liam O'Neill.
Liam O'Neill previously worked as Associate Director Risk and Compliance at Gsk and Associate Director - Site Operations (Harlow and Addenbrookes) at Gsk. Liam O'Neill holds Bachelor Of Arts (Honours) In Business Management (Leadership Practice), Upper Second-Class Honours (2.1) from The Open University.
Email format at GSK
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AeroLeads found 1 current-domain work email signal for Liam O'Neill. Compare company email patterns before reaching out.
About Liam O'Neill
As the GSK Associate Director Risk and Compliance for the Europe R&D sites, I am responsible for ensuring that GSK’s principle and enterprise risks are managed appropriately by the R&D Engineering Services organisation and that local ways of working are in accordance with Corporate Policies, QMS (Quality Management System) Policies and Corporate Compliance programs (Risk Management, Info Protect, Third Party Oversight). I not only ensure that the strategies for implementation are effective but also verify through the Internal Control Framework assessment process to ensure no residual risk remains.At the weekend, I am also the head coach for BabyBallers Bishop’s Stortford Ltd. BabyBallers is a children's football and multi-skills club for ages 16 months - 5 years.
Listed skills include Dangerous Goods, Adr, Iata, Hazardous Materials, and 29 others.
Liam O'Neill's current company
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Liam O'Neill work experience
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Associate Director - Site Operations (Harlow And Addenbrookes)
Responsible for hard, soft, and scientific services at GSK Harlow and Addenbrookes sites. Overseeing capital investment and own the rolling infrastructure capital plan. The purpose of this role is delivery of buildings and services that are safe, legal and compliant.Partnering with respective local and global R&D business leaders responsible for the sites.
Pharma R&D Quality For The Patient Lead
Leading the GSK Pharma R&D Quality for the Patient (Q4TP) team. Q4TP is a group comprising of representatives from R&D across EMEA, America's, and APAC.Our mission statement is “Enhancing a culture of Quality mind-set by educating, engaging, and motivating our colleagues about the work they do in service of our Patients”.Our role is to convey the Quality.
Compliance Specialist
- Quality Management System:
- Competent Deviation business lead investigator and trainer, including mentoring others; lead RCAs and development of ASMART CAPA
- CAPA and CAPA Effectiveness Check owner and mentor for GSK and its Service Partner staff
- Develop annual GSK Management Monitoring Universe, Schedules and execute management monitoring assessments (both GxP and non-GxP). Authors annual GxP Management Monitoring Effectiveness Check. Reports on schedule.
- Risk Management: Own compliance related risks, assist staff to enter records into risk management system; deliver risk management training
- Reviews and Owns Quality Management System SOPs, as a representative, during ad-hoc revisions or periodic review, for compliance to regulations. Communicates changes to stakeholders including potential impact to GSK.
Supplier And Audit Specialist
My responsibilities included working with operations to ensure vendor compliance, raise and investigate vendor complaints, writing and management of Quality Agreements, leading deviation investigations relating to suppliers and conducting vendor assessments.I lead the UK internal audits on PerkinElmer activities on GSK R&D and Consumer Health sites which.
Supplier And Audit Specialist
As the Supplier and Audit Specialist for CBRE working on the GSK account. I specialised in vendor compliance and auditing. My responsibilities included working with operations to ensure vendor compliance, raise and investigate vendor complaints, writing and management of Quality Agreements, leading deviation investigations relating to suppliers and.
Interim Site Lead & Customer Business Manager
- Drive operational control through Metrics/KPI Management.
- Maintain a Site budget to identify variations and support action planning.
- Site financial forecasting requirements and ensures compliant financial practices to ensure on time and compliant billing.
- Monitors recurring spend to identify saving opportunities (Labour/Sub/Materials, Optimize Self Perform utilization, Control Variable spend).
- Supports initiatives to achieve/exceed budget expectations at the site level.
- Manages accurate asset inventory & Life Cycle Assessment, including identification and support of Capital replacement projects.
Facilities Manager
- Audit all soft and hard services to ensure standards are being maintained.
- Drive operational control through Metrics/KPI Management.
- Maintain a site budget to identify variations and support action planning.
- Supports site financial forecasting requirements and ensures compliant financial practices to ensure on time and compliant billing.
- Supports initiatives to achieve/exceed budget expectations at the site level.
- Ensure accurate asset inventory & Life Cycle Assessment, including identification and support of Capital replacement projects.
Technical Writer
My role within the Compliance Team is to complete periodic reviews of SOP’s for Facilities at MSD Hoddesdon. These would include Laboratory Services, Calibration, Validation, Engineering, Maintenance and GMP cleaning. I am responsible for seeing investigations into deviations and the subsequent CAPA’s through to completion.
Dangerous Goods Safety Advisor And Waste Manager
I managed the waste streams at MSD Hoddesdon. This involved classifying waste, managing contracts of waste vendors and ensuring site compliance to national and corporate regulations of Hazardous and non-hazardous waste.As DGSA I was responsible for writing procedures governing the site's activities ensuring compliance of national and corporate regulations.
Dangerous Goods Safety Advisor And Waste Co-Ordinator
The role was to ensure compliance with both national and corporate regulations governing Dangerous Goods by Road, Air and Sea as well as assisting the site Safety and Enviornment department in compliance of Hazardous and Non-hazardous waste.This involves writing policies and procedures as well as documenting and investigating any non compliance.
Laboratory Technician
Worked in the Laboratory Services and Materials Management department. Job duties were classifying and packing of dangerous goods for road and air transport, sampling and dispensing of raw materials and API for the science and chemistry departments and receiving materials into the inventory control system. Promoted to the newly created role of DGSA and.
Liam O'Neill education
Bachelor Of Arts (Honours) In Business Management (Leadership Practice), Upper Second-Class Honours (2.1)
National Diploma Sport
Education record
Frequently asked questions about Liam O'Neill
Quick answers generated from the profile data available on this page.
What company does Liam O'Neill work for?
Liam O'Neill works for GSK.
What is Liam O'Neill's role at GSK?
Liam O'Neill is listed as Associate Director Risk and Compliance at GSK R&D at GSK.
What is Liam O'Neill's email address?
AeroLeads has found 1 work email signal at @cbre.com for Liam O'Neill at GSK.
Where is Liam O'Neill based?
Liam O'Neill is based in Stevenage, England, United Kingdom while working with GSK.
What companies has Liam O'Neill worked for?
Liam O'Neill has worked for Gsk, Perkinelmer, Inc., Cbre Global Workplace Solutions (Gws) Emea, and Johnson Controls.
How can I contact Liam O'Neill?
You can use AeroLeads to view verified contact signals for Liam O'Neill at GSK, including work email, phone, and LinkedIn data when available.
What schools did Liam O'Neill attend?
Liam O'Neill holds Bachelor Of Arts (Honours) In Business Management (Leadership Practice), Upper Second-Class Honours (2.1) from The Open University.
What skills is Liam O'Neill known for?
Liam O'Neill is listed with skills including Dangerous Goods, Adr, Iata, Hazardous Materials, Hazardous Waste Management, Waste Management, Sop Authoring, and Sop Development.
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