Meet the Team
Meet the Team
Management
Morgan O'Brien
General Manager Europe
With over 20 years of project experience in the Pharmaceutical and related industries, Morgan has held a number of Project and Commissioning Management roles on high value projects both in Asia and Europe. P.M.P. certified with the Project Management Institute, and this along with his practical, in-the field experience have allowed him to understand the requirements of successful Project Delivery.
JoonLeong Ng
Business Director Singapore
With 15 years of experience across APAC region with focus on Commissioning, Qualification & Validation in the pharmaceutical industry. Throughout the years, Joon has gathered extensive hands-on as well as management experience. He also possesses in depth knowledge in Regulation & Guidelines, Project Management, Change Control Process and Lean Leadership.
Frank Yao
Business Support
Hans van den Hoogen
C&Q Engineer
Hans van den Hoogen has over 10 years of experience in the pharmaceutical industry, specializing in CQV and held multiple lead positions.
As a certified Power User Level 2 in Kneat, he has supported client projects in adopting digital tools for CQV, driving efficiency and innovation in industry operations.
Chia Ren Jie
Business Manager
With a degree in Chemical Engineer at the National University of Singapore, Renjie built his expertise in biopharma manufacturing and CQV, specialising in downstream processes. Today at No deviation, he applies that technical depth to business development and partnership management, connecting opportunities and people with the same care and precision that define the life sciences industry.
Hong Hwee Lim
Business Manager
With over 12 years in pharmaceutical manufacturing and validation, Hong Hwee leads client engagement, proposal development, and project delivery across GMP-regulated facilities. She brings expertise in equipment qualification, compliance assessments, and project coordination, ensuring both technical and regulatory excellence. She has a strong track record of driving performance and compliance through technical depth and business insight.
Technical Staff - Singapore
Qian Dong Heng
Technical Lead, Knowledge Management
Qian Dong Heng is a Process and Automation Engineer with over five years of experience across the pharmaceutical and oil & gas industries. As Technical Lead for Knowledge Management at No deviation, he brings strong expertise in risk assessment, cGMP compliance, and validation activities, including computer systems, cleaning, and process validation.
Shanta Latchumy
Technical Lead
Shanta is a Kneat Super User and validation specialist with strong experience in commissioning, qualification, GMP documentation and paperless validation. At No deviation, she supports Kneat deployment, governance and continuous platform support, combining hands-on project experience with a detail-oriented and knowledge-sharing mindset.
David Bartlett
Automation Technical Lead
SME Automation and Senior Manager at No deviation, David is leading critical conversations around digital transformation. As ISPE Singapore’s Pharma 4.0 Community of Practice co-founder and its Automation SME, he brings hands-on experience and sharp insight into the evolving landscape of pharma manufacturing as the “Digital Reality” track’s session chair and panelist.
Augustus Graham
Process Technical Lead
Originally from Kansas, USA, he holds a degree in Chemical Engineering from Kansas State University and began his career with Pfizer (formerly Hospira) in the US and India. Since moving to Singapore in 2017 and joining No deviation in 2019, he has worked on major biopharma projects, including GSK’s vaccine expansion, where he leads the upstream equipment scope from design to qualification.
Technical Staff - Europe
Hong Hwee Lim
Lead Accountant
An experienced Lead Accountant with a demonstrated history of working in the pharmaceuticals/engineering industry. He has an acute understanding of business practices and is skilled in utilizing tools to achieve desired results.
Dave O' Connor
C&Q Digital Transformation Manager
Dave O’Connor is a CQV consultant with extensive experience in Project Management, Compliance and Equipment Commissioning, Qualification & Validation (CQV) in Med-Device, API and Biotech Manufacturing. He regularly contributes to the ISPE Digital Validation subcommittee and has published several articles on the subject of Digital Validation Tools (DVT’s). He is a Chapter Lead for the upcoming ISPE Good Practice Guide for Digital Validation Tools, due to be published in Q2-2025.
Mary O' Brien
CQV Specialist
Mary has over 20 years experience working in numerous projects in the Bio-pharmaceutical and food industries. A Senior C&Q Lead Engineer with previous management experience including as a Suite Team Lead. A member of the No deviation Kneat development team with a strong understanding of the key elements associated with the Kneat Gx platform, holding Kneat Power Level 2 and Kneat Administrator Certification.
Chloe Lu
Human Resource Executive
Chloe is a Human Resource Executive who has experience in the F&B, retail and pharmaceuticals/engineering industries. She manages the full spectrum of HR functions, is responsible for implementing policies and is the go-between employees and employer.
