Wide-ranging Facility experience
I have first hand experience of acting as QP at MIA, MIA(IMP), and
MS sites, including IMP QP oversight for UK. I’ve set up PQS for QP
Importation facilities from scratch in both UK and Ireland, obtaining
regulatory licences and importing products from tablets to ATMPs
into UK/EU. I’ve worked through the commercialisation of mutiple
products, including live viral vaccines, ex-vivo CAR-T vectors, and
CRISPR-Cas9 ATMPs, facilitating MHRA & FDA PAI inspections,
including response and CAPA plans.
Product Experience - including ATMPs
I’ve worked for a global client base (especially US / EU / UK), from
big pharma to small CMOs and virtual biotech startups - with
products ranging from tablets and capsules to injections, ATMPs,
cell banks (CHO for mAbs), virus seeds, live virus vaccines, COVID
vaccines, cell and gene therapies including hESCs, T-cells, CAR-T,
and CRISPR Cas-9 editing, and viral vectors including HSV and
lentivirus. This informs our service offering across an unusually
wide range of biological and chemical products - hence the name BioChem!
Deep understanding of Analytical QC
I started in GMP within the QC lab. I’m an MSc Qualified Analytical
Chemist, spending several years in the API QC labs at Zeneca. In
addition to chemical QC expertise (chromatography, spectroscopy,
etc), I have over 20 years experience with biological QC testing,
including molecular biology techniques, immunology-based
testing, virology, and microbiological QC testing, as well as specific
ATMP techniques including cell-based potency assays, genetic
sequencing, and flow cytometry.
Passion for applying Maths and Stats
Any of my clients will confirm how much I love looking at an SPC or
trend chart, on pretty much any topic. I’m well-versed in Excel, and
other more capable statistical software including Minitab and SPC
for Excel. I have an enduring interest in the application of statistics
(good and bad) to aspects of process control, QMS performance,
sampling, analytical and process validation, and anything else I can
find a use for. If you can’t measure it you can’t hope to control it!
Continuous Learning and Development
One of the best things about being a Contract QP is that you get
to set your own training budget! Since 2010 I’ve attended
multiple training / CPD events every year - including MHRA &
HPRA symposia, aseptic processing / Annex 1 events, PQG
events, Pharma Law updates, ATMP manufacturing, AI in
Pharma, etc. During that time I’ve also completed an OU Honours
Module in Cell & Molecular Biology (2016), and a Masters diploma
in ATMPs from the University of Granada (2024). I’m also member of multiple
professional associations, including PHSS, PQG, and PDA with access to their
technical resources
Full IT and Software Capabilities
I never rely solely on my client companies to provide me with the
hardware and software I need to provide a great service. I have my
own IT equipment with full Office365 business suite (Outlook,
Office, OneDrive, Teams, etc), as well as my own subscriptions to
USP and EP - essential for any contract QP. I also have Visio (can’t
beat a good process map), MindManager for mind-mapping (still
the best way to organise and link thoughts), and timesheet
software for clear detailed invoices.