Uvitech · Automation
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About Uvitech

An engineering company built around regulated manufacturing.

UVITECH LTD. is a London-based systems integrator. We specialise in automation and process control for Life Science customers, and we deliver projects wherever those customers manufacture.

London · HQThe City of London skyline
Engineers reviewing drawings together at a table

What we believe

Good automation is quiet.

A well-integrated control system is one nobody talks about: cycles complete, records are produced, audits pass. Getting there takes a narrow focus, so we limit ourselves to the two things we do best and say no to the rest.

We work as an extension of your engineering and QA teams rather than as an outside vendor. That means shared specifications, witnessed tests, and documentation written for the people who will use it in five years.

How we work

The same sequence on every project.

A fixed lifecycle keeps small projects fast and large projects predictable. Each phase closes with a reviewed document.

  1. 01

    Discover & specify

    Site visit, process review and a User Requirements Specification written with your engineering and QA teams.

  2. 02

    Design

    Functional and design specifications, architecture, risk assessment and traceability back to every requirement.

  3. 03

    Build & test

    Panel build and software development, then a witnessed Factory Acceptance Test before anything ships.

  4. 04

    Commission & qualify

    Installation, SAT, IQ/OQ support, training and handover, followed by remote support.

Global reach

Where we deliver.

Projects are engineered and tested in the UK, then commissioned on site by the same engineers. Between visits, systems are supported remotely through secure, customer-controlled access.

United Kingdom & Ireland

Head office and engineering. Short-notice site visits.

HQ · London
Continental Europe

Pharmaceutical and biotech sites across the EU and Switzerland.

On-site · Remote
North America

US and Canadian manufacturers; documentation aligned to FDA expectations.

On-site · Remote
Middle East

Greenfield facilities and equipment upgrades.

On-site · Remote
Asia-Pacific

OEM equipment commissioning and control retrofits.

On-site · Remote
Focus

Life Science only

Pharmaceutical, biotech, sterile fill-finish, medical devices and laboratories. No other sectors.

Independence

Vendor-neutral

We select platforms on lifecycle support and your site standards, not on reseller agreements.

Continuity

One lead engineer

The engineer who writes the specification is the one who commissions the system.

Start a conversation

Tell us about your process. We will tell you how we would automate it.