Pierre Winnepenninckx

Pierre is a Chemical Engineer and the CEO of No deviation. He likes to develop a team vision for quality accountability and innovation. He is hugely optimistic and sees the opportunity in every task he undertakes.

A pharmaceutical engineer conducting GMP-compliant maintenance on manufacturing equipment, ensuring process control and regulatory compliance.

GMP-Compliant Maintenance: A Pillar of Process Control

1 Comment / Blog, Predictive Maintenance /

GMP-Compliant Maintenance: A Pillar of Process Control In Good Manufacturing Practice (GMP), the third phase of process validation—continued process verification—ensures that your process remains in a state of control. However, maintaining this state is not static; it requires proactive management throughout the lifecycle of your facility. From the initial equipment qualification and process validation, many changes will inevitably occur. Equipment…

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Nd Conversations That Matter

Mobilizing a Digital Engineering Program: Practitioner View   

Leave a Comment / Blog, Digitalization /

Conversations That Matters No deviation’s  Takeaways from ISPE Facilities of the Future Conference in San Fransisco Mobilizing a Digital Engineering Program: Practitioner View    Speaker: Joydeep Ganguly, Gilead Sciences, Inc.   Gilead Sciences: Rebuilding for Innovation and Digital Transformation  Gilead’s ambition to lead pharmaceutical innovation drove its strategic decision to accelerate drug development and optimise operational efficiency.

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Nd Conversations That Matter

Revolutionizing Pharmaceutical Manufacturing: Robotics, Teleoperation, and Digital Twins

Leave a Comment / Blog, Digitalization /

Conversations That Matters No deviation’s Takeaways from ISPE Facilities of the Future Conference in San Fransisco Shanshan Liu, our technical director and Pierre Winnepenninckx, our CEO were attending ISPE Facilities of the Future conference 2025 happening last week! Here’s a summary of the sessions they attended on Robotics, teleoperation and ditigal twins. Introduction This content summarizes

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the 7 guides to unlock a successful risk based cqv project no deviation

The 7 guides to unlock a successful risk-based CQV project

Commissioning, Qualification and Validation /

Our previous post talked about the skills a CQV engineer needs. In this article, we will give you the CQV starter kit with 7 documents that will guide you in unlocking a successful risk-based CQV project. It has everything you need to understand the journey of equipment into the different phases of the project, and

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what you need to become a cqv engineer in the pharma industry no deviation

What you need to become a CQV engineer in the pharma industry

Blog, Commissioning, Qualification and Validation /

In our previous posts, we explained why there is no better time than now to work in the pharmaceutical industry. It is especially true for the year to come, if you live in Singapore or plan to relocate here. With the current COVID-19 situation, much more manufacturing power is needed, and Singapore is a unique

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the triangle no deviation

How to reach a quality mindset in the pharma industry

Blog, Quality and Compliance /

In the pharmaceutical industry, quality is one of the foremost considerations. Technological evolution has enabled new ways of delivering quality, which go beyond compliance. In fact, a proactive approach will help create the greatest value for the patient and for the pharma company. For this, a quality mindset must be achieved. This diagram represents how,

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digitalisation in the pharmaceutical industry no deviation

Digitalization in the pharmaceutical industry

Blog, Digitalization /

Last year during the ISPE Singapore conference 2020, I was fortunate to moderate a discussion on Reaching Digital Maturity Through Pharma 4.0. I shared the panel with Roger Harty, Director of EMEA & APAC, Belgium, Samme Wang, Head of Engineering and Technology Asia, Bayer, Singapore, Rajnish Narula, Director Business Excellence, Pfizer, Singapore, Jennie Burton, Operations

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