With over 35 years of hands-on experience in highly regulated industries, I provide senior-level technical consultancy to pharmaceutical, biotech, medical device, chemical and nuclear organisations across the UK and Europe.
My background in Chemical Engineering underpins everything I do — from writing bulletproof validation documentation to leading complex capital projects and steering teams through regulatory inspections. I don’t just consult; I embed, deliver, and leave your organisation stronger than I found it.
I have worked on-site and remotely with some of the world’s most recognised names in the life sciences sector, including GSK, Pfizer, AstraZeneca, MSD and Johnson & Johnson, as well as numerous specialist contract manufacturers and engineering firms.
Where I Work
I am based in the UK and available for on-site engagements, remote support, and long-term embedded contracts across Europe.
I have extensive experience working in multinational, cross-border environments and am fully conversant with international regulatory frameworks including FDA (21 CFR), EU GMP, EMA guidelines, and MHRA requirements.
Countries I have worked in include:
United Kingdom · Ireland · Netherlands · Belgium · Germany · France · Denmark · Switzerland
I am comfortable operating in diverse cultural and organisational environments, and have a proven track record of integrating quickly into client teams — whether for a focused two-week documentation sprint or a multi-year capital project.
Currently available for new engagements across the UK and EU. On-site preferred; remote and hybrid arrangements considered.