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Serialisation engineer

Crawley
Blackfield Associates
Engineer
Posted: 9 March
Offer description

Serialisation Engineer

West Sussex

Are you looking to build specialist expertise in serialisation and automation within a regulated pharmaceutical environment?

We're recruiting a Serialisation Engineer to join a global life sciences organisation supporting clinical trials and pharmaceutical supply chains. This is an excellent opportunity to develop hands-on experience with industry-leading serialisation and compliance systems while contributing to medicines and therapies that impact patients worldwide.

Working within a collaborative engineering and operations team, you'll gain structured training and exposure to real production challenges, helping you progress towards becoming a Subject Matter Expert (SME) in serialisation technologies.

The Role

In this role you will support and develop serialisation systems used within pharmaceutical packaging and supply chain operations.

Key responsibilities include:

* Operating and supporting serialisation systems in line with SOPs, GMP and engineering best practices
* Investigating and resolving serialisation issues, including data recovery and file repair
* Creating and maintaining serialisation equipment recipes for production
* Retrieving and analysing data from automation and serialisation systems
* Supporting engineering validation and connectivity testing
* Working closely with engineering, quality, operations teams and external suppliers
* Assisting with preventative maintenance activities and machine breakdown support
* Contributing to continuous improvement initiatives across production and quality
* Ensuring all work is completed safely and in line with compliance standards

What We're Looking For

We're looking for someone who is curious, technically minded and motivated to develop within a regulated engineering environment.

You will ideally have:

* A relevant engineering qualification or equivalent practical experience
* Strong analytical and problem-solving skills
* Good organisational and time management abilities
* The ability to work both independently and collaboratively
* Clear communication skills when working with cross-functional teams
* Proficiency in Microsoft Office (Word, Excel etc.)

Experience in pharmaceutical, manufacturing, or other regulated industries would be advantageous, but not essential.

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