Manufacturing Execution System (MES) Engineer

Operations Helix Ltd

Glasgow, United Kingdom

20 days ago

Role details

Contract type

Permanent contract

Employment type

Full-time (> 32 hours)

Working hours

Regular working hours

Languages

English

Experience level

Intermediate

Compensation

£ 46K

Job location

Remote

Glasgow, United Kingdom

Tech stack

C Sharp (Programming Language)

SQL Databases

Data Streaming

XML

Microsoft Power Automate

Information Technology

GXP

Servicenow

Job description

Working onsite with a key Operations Helix Ltd client you will support the use of the MES system in the manufacturing environment. This includes change management, troubleshooting and continuous improvement activities, ensuring the site delivers safe and effective products that whilst maintaining compliance. The MES engineer will provide subject matter expertise to the operations team for day-to-day production and project work to ensure that output targets are met in line with the production plan., * Provide SME knowledge to the operations team with respect to the MES system.

Partner with Operations, Supply Chain, Engineering, IT and Quality functions to ensure efficient and effective MES site support during operational hours.
Support MES-related documentation, training, and user onboarding
Assist in the rollout of MES upgrades, patches, and system enhancements
Monitor MES interface with lab systems, ERP, and production equipment to ensure data flow and integrity.
Ensure all activities align with GxP compliance and quality assurance protocols.
Design, author, develop and configure Electronic Batch Records (EBR).
Implement MES solutions and integrate with ERP and control equipment.
Document MES configuration and validation of EBRs.

Requirements

Do you have experience in ServiceNow?, Do you have a Bachelor's degree?, * Bachelor's degree in Computer Science / IT/ Pharmaceutical Manufacturing/Engineering, or a related technical field.

Minimum 3 years' MES implementation experience within GMP-regulated environments.
Full understanding of cGMP requirements including 21 CFR 11 and Annex 11.
Excellent understanding of GAMP principles, systems implementation and validation concepts.
Experience with POMS system is advantageous.
Strong C# coding and SQL Database knowledge required.
PTL, XML and Power Automate knowledge desirable.

If you're passionate about supporting digital operations that drive pharmaceutical innovation and quality, we'd love to hear from you. Join a team where your technical skills make a direct impact on patient outcomes and product excellence., * MES: 3 years (preferred)