Pharma Serialisation Engineer: Automation & Compliance

Blackfield Associates; England; On-site; GBP 40,000 - 60,000; Full time

Job summary

A global life sciences organisation is seeking a Serialisation Engineer in the UK to support and develop serialisation systems used in pharmaceutical packaging. Candidates should have a relevant engineering qualification, strong analytical skills, and the ability to work in a collaborative environment. This role offers structured training and hands-on experience in a regulated setting, contributing to critical aspects of clinical trials and pharmaceutical supply chains.

Qualifications

• Curiosity and motivation to develop in a regulated engineering environment.
• Experience in pharmaceutical or manufacturing industries is advantageous.

Responsibilities

• Operate serialisation systems in line with SOPs and GMP.
• Investigate and resolve serialisation issues, including data recovery.
• Create and maintain serialisation equipment recipes.
• Retrieve and analyse data from automation systems.
• Support engineering validation and connectivity testing.
• Work closely with engineering, quality, and operations teams.
• Assist with preventative maintenance activities.
• Contribute to continuous improvement initiatives.
• Ensure all work complies with safety and standards.

Skills

Strong analytical and problem-solving skills

Good organisational and time management abilities

Ability to work independently and collaboratively

Clear communication skills

Proficiency in Microsoft Office

Education

Relevant engineering qualification or equivalent practical experience

Job description

A global life sciences organisation is seeking a Serialisation Engineer in the UK to support and develop serialisation systems used in pharmaceutical packaging. Candidates should have a relevant engineering qualification, strong analytical skills, and the ability to work in a collaborative environment. This role offers structured training and hands-on experience in a regulated setting, contributing to critical aspects of clinical trials and pharmaceutical supply chains.