MES SME
 |
Job Type | Contract |
This role sits within the Global Team of a top 5 Pharma client. The role is fully remote and gives you the opportunity to work with projects across the world.
Requirements
We are seeking an experienced AI & Manufacturing Execution Systems (MES) Subject Matter Expert to join a global team driving the adoption of AI across Automation, IT, and MES functions within a leading pharmaceutical manufacturing organisation.
This is not a project-based role. Instead, you will play a key part in shaping the organisation’s long-term AI strategy, identifying opportunities to reduce workload, improve productivity, and standardise processes by integrating AI into MES operations while ensuring all quality and validation decisions remain human-led.
Working within a global centre of excellence, you will help evolve how AI is utilised across manufacturing, supporting the development of scalable, compliant, and efficient processes.
Key Responsibilities
Act as the SME for the application of AI within MES and manufacturing processes.
Develop effective AI prompts and workflows using tools such as Microsoft Copilot, Claude, and Claude Cloud to generate high-quality outputs.
Validate and verify AI-generated content to ensure accuracy, GMP compliance, and alignment with global standards.
Support the creation of MES recipes and documentation using AI-assisted approaches.
Identify opportunities to expand AI adoption across manufacturing operations and business processes.
Use AI to generate initial design documentation from engineering and process data.
Ensure recipes, procedures, and documentation remain aligned with global standards and avoid process drift.
Leverage AI to create, review, and verify code where appropriate.
Review AI-generated recipe changes and assess the potential impact on regression testing and downstream manufacturing processes.
Support the development of approved text, scripts, and standardised content for MES applications.
Collaborate with global Automation, IT, and MES teams to continuously improve AI capabilities and governance.
Required Experience
Strong background within pharmaceutical manufacturing operating in a GMP-regulated environment.
Proven experience working with Manufacturing Execution Systems (MES).
Experience with Syncade and/or PharmaSuite is highly desirable.
Strong understanding of MES recipe design, procedures, and manufacturing documentation.
Experience validating technical documentation, recipes, or manufacturing processes.
Ability to translate business or manufacturing requirements into effective AI prompts and validate AI-generated outputs.
Excellent analytical and problem-solving skills with a continuous improvement mindset.
Strong stakeholder management and communication skills within global teams.